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Fragrance Terms

Aromatic and Herbaceous

The term 'aromatic' is sometimes used, especially by laymen, to refer to the assertive, fresh fragrance produced by sweet balsamic and resinous green-herbal notes, such as that of pure lavender essence. But strictly speaking, it means an organic compound with a benzene (or arene) hydrocarbon ring structure. The name was originally given to these compounds, before their chemical structure was known, because of their somewhat sweet scent. Aromatic notes are not typically syrupy sweet, but are not at all bitter either. Aromatic compositions are most typically found in fragrances for men.

Herbaceous aromatic materials pair quite well with citruses and spices, in that way lending themselves to fragrances for women as well as unisex perfumes, in addition to the better known masculine ones. Lavender is the prototypical aromatic substance and is used very commonly in perfumery. With its pleasant association with the outdoors and cleanliness, it is a mainstay of the fougère/fern family and frequently is combined with ferny smells with which it has overlapping qualities. The term 'aromatic fougère' is used especially with masculine fragrances, forming a subclassification typified by heavier use of cool, refreshing herbal top notes. Yves Saint Laurent Rive Gauche pour Homme is the perfect example of this genre.

Aromatic accents are used with classic cologne-like notes, providing a somewhat sharper, tonic scent such as that of the 4711 Acqua Colonia series, and are also used to provide a contrasting brightness with darker resinous notes such as incense, as is found in Serge Lutens Encens et Lavande.

In addition to lavender, herbal contributors of aromatic-green camphorous notes, frequently used together in combination, include rosemary and sage, present for example in the top notes of Dior Eau Sauvage, Caron pour Un Homme, and Guerlain Habit Rouge, as well as cumin, mugwort, star anise, and other plants with a very intensive grassy-spicy scent. Examples include artemisia, basil, estragon, marjoram, peppermint, tea, and tobacco.

Other well-known fragrance products with a prominent aromatic nature include:

Acca Kappa White Moss
Acqua di Parma Blu Mediterraneo series
Alfred Dunhill Pure
Alt-Innsbruck Eau de Cologne
Amouage Sunshine Men
Annick Goutal Eau de Lavande
Aramis A, Black, and New West for Him
Atkinsons Rockford and Sport Blue Sky
Aubusson Man in Blue
Azzaro Aqua Verde and Pour Homme LE 2014
Baruti Berlin Im Winter
Borsari Acqua della Macchia Mediterranea
Brooks Brothers New York for Gentlemen
Burberry Summer for Men
Bvlgari Eau Parfumee au The Bleu
By Kilian Moonlight in Heaven
Calvin Klein Eternity Summer and Reveal Men
Caron Pour Un Homme
Caswell Massey Michelsen's Bay Rum
Christian Dior Fahrenheit Summer 2006 and Eau Sauvage
Claus Porto Agua de Colonia No. 4 Spearmint Tea
Coty Gravity series
Crabtree & Evelyn Black Absinthe
Creed Silver Mountain Water
Davidoff Cool Water Freeze Me
Flamboyant Royal White
Floris Lavender
Giorgio Armani Code Ice and Diamonds Summer Fraiche
Givenchy Insense series
Hermes Eau de Gentiane Blanche
Jil Sander Ultrasense
Kenneth Cole Blue and New York Men
Marbert Man Personality
Masaki Matsushima M
Maurer & Wirtz 4711 series
Paco Rabanne Ultraviolet series and XS Sensual Summer
Paul Sebastian Fine Cologne
Penhaligon's Douro and Lavandula
Perry Ellis 360 Degrees and Portfolio Green
Pierre Cardin Vertige
Ralph Lauren Polo Red White & Blue
Roger & Gallet L'Homme
St. Charles Shave Bulgarian Lavender
Santa Maria Novella lavanda Imperiale, Porcellana, Potpourri
Serge Lutens Laine de Verre
Taylor of Old Bond Street Luxury Lavender Water
The Body Shop White Musk
Tom Ford Lavender Palm
Truefitt & Hill 1805
Yves St. Laurent Kouros Eau d'Ete 2006

The term 'herbaceous' often is used more broadly to refer to components derived from or reminiscent of herbal plants in general, which produce a naturally cool, dry, leafy, or hay-like note, such as chamomile, lavender, rosemary, or clary sage. The term 'grassy' is used to refer to a similar but different green, sharp tone like the scent of a freshly mowed lawn or crushed green leaves. Examples include the fragrances of Balmain Vent Vert and L'Artisan Premier Figuier. It should be noted, however, that 'herbaceous' and 'grassy' are not exactly the same as 'aromatic.' Purely herbaceous or grassy materials typically are cool (and especially produce that sensation when blotted and pressed to the lips), while more characteristically aromatic substances tend to be spicy and warm.
 
Mint/Menthol/Coolness

Citrus, green leaves, tart fruit, and lily of the valley are all described as cool scents, but most are not actually cooling. While a 'cool' perfume merely evokes pleasant associations, a truly 'cooling' one is instantly refreshing. The mint family is characterized by this invigorating 'cooling' effect. Menthol, the main component of mint essence or essential oil, provides the trigger for this through TRPM8 cold-sensitive skin receptors. The essential oil of all mint types is extracted from the plants through steam distillation. The oils are clear to pale yellow, with watery viscosity. The mint group includes Japanese mint, English mint, apple mint, curly mint, pennyroyal, peppermind, pineapple mint, spearmint, and water or bog mint, among others. The most important ones commercially are peppermint (M. piperita), spearmint (M. spicata), and wild/field/corn mint (M. arvensis).

In general, mint provides a fresh lift to all fragrance types, accenting the top note. It combines well with white flowers, especially with orange blossom and jasmine, which it also balances. It has become more important as a single note in some modern products that feature 'natural' market positioning. Until fairly recently it was rarely used much in perfumery, probably because of the fact that a fragrance with a bright minty note tends to evoke associations with toothpaste or other hygiene products. Other than Guerlain Aqua Allegoria Herba Fresca or Mentafollia and certain summer limited editions like Cologne Le Male Summer, the majority of experiments with a dominant mint note have just been in minor niche perfumery. Fragrances with the subgroup smell of mint cocktails can be allocated into separate collections: mojito, caipirinha etc. Such accords can be found in vintage Calvin Kline Crave, L’Artisan Parfumeur Batucada, Tom Ford Costa Azzurra, A Lab on Fire Eau d’Ipanema, Demeter Caipirinha, Pierre Guillaume Croisière Mojito Chypre, and Guerlain Homme. Mint essential oil or menthol also can be a part of fresh citrusy accords, such as Diptyque Oyedo.


Mint

Mint (also known as mentha, from the Greek 'míntha' for the nymph that Pluto turned into a sweet-smelling herb), with over 40 species and hybrids, is a genus in the family Lamiaceae. The Lamiaceae (or Labiatae) are also known as the deadnettle family or sage family. Many of them, including widely used culinary herbs like basil, rosemary, sage, savory, marjoram, oregano, hyssop, thyme, lavender, and perilla, are aromatic in almost all their parts. These flowering plants can be shrubs, trees (such as teak), or rarely vines. Besides those grown for their edible leaves, some are grown for decorative foliage, such as Coleus. Others are grown for seed, like chia, or for their edible tubers, such as various exotic potatoes and Chinese artichoke.
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The alternative family name Labiatae refers to the fact that the flowers typically have petals fused into an upper lip and a lower lip ('labia' in Latin). The flowers are bilaterally symmetrical with five united petals and five united sepals. They are usually bisexual and verticillastrate (a flower cluster that looks like a whorl of flowers, but actually consists of two crowded clusters). The leaves emerge oppositely, each pair at right angles to the previous one (decussate) or whorled. The stems are frequently square in cross section, but this is not found in all members of the family.

The family has traditionally been considered closely related to the Verbenaceae (verbena or vervain family), and in the 1990s, phylogenetic studies suggested that many genera classified in the Verbenaceae actually should be classified in the Lamiaceae or in other families of the order Lamiales.


Peppermint and Spearmint

Peppermint (Mentha × piperita, also known as Mentha balsamea wild.) is a hybrid mint, a cross between water mint and spearmint, with spearmint already being a hybrid itself. Peppermint is occasionally found in the wild with its parent species. While Western peppermint is derived from Mentha piperita, Chinese peppermint (or 'Bohe') comes from the fresh leaves of Mentha haplocalyx.
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Peppermint is indigenous to Europe and the Middle East, but it has been cultivated since the late 17th century and is mainly a cultivated species now. Cultivated plants have been selected for more and better oil content. Outside of its native range, areas where peppermint was formerly grown for essential oil often have an abundance of feral plants, and it is considered invasive in Australia, the Galápagos Islands, New Zealand, and the Great Lakes region of the U.S.

There are two main types of peppermint: black mint (also called English mint or mitcham mint) (rubescens nigra) and white mint (pallescens alba). Black mint provides most of the essential oil. The plant is generally harvested before it blooms, when it has the highest oil content, and/or during dry, sunny weather. It usually is harvested in the morning before the oil content is reduced by the sun.

The oil is obtained with steam distillation of the whole plant. The essential oil is nearly colorless. Usually, the shorter the distillation process, the higher the menthol content and the quality of the oil. Analysis of the chemical composition of the essential oil from peppermint (Mentha × piperita L.) demonstrates the main constituents to be menthol, menthone, and menthyl acetate, with the latter responsible for the minty aroma and flavor. The oil most often undergoes additional fractionating to remove unwanted components, such as the lightest fraction containing the unpleasant-smelling dimethyl sulfide. Japanese peppermint oil typically contains 85% menthol, while English oil has 60-70% and American oil 50-78%.

Black mint is cultivated in England, France, Germany, Argentina, Brazil, Romania, Hungary, Poland, Morocco, India, Ukraine, and many other locales. Peppermint is the most commonly used of the more than 25 species of the genus Mentha. In 2000-2006, world production was led by the United States, but more recently (2014) it has been claimed that Morocco and Argentina produce the largest harvests. In the United States, Oregon and Washington produce most of the country's commercial peppermint.
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White peppermint is less hardy and less productive. It is an evergreen perennial that is similar to the black type but is a lighter shade of green and lacks the red or purple flush that appears on leaves and stems of the black variety. White peppermint essential oil, more delicate in aroma, is quite rare.
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Peppermint was first described scientifically in 1753 by Carl Linnaeus from specimens that had been collected in England. He treated it as a species, but it is now universally agreed to be a hybrid. It is an herbaceous rhizomatous perennial plant that grows to be 30–90 cm tall, with smooth stems. The rhizomes are wide-spreading, fleshy, and bear fibrous roots. The leaves are downy and dark green with reddish veins, and they have an acute apex and coarsely toothed margins. The leaves and stems are usually slightly fuzzy. The flowers are white or purple, with a four-lobed corolla. They are produced in whorls around the stem, forming thick, blunt spikes. Flowering season lasts from mid- to late-summer. Peppermint is a fast-growing plant; once it sprouts, it spreads very quickly. Wild peppermint typically appears in moist habitats, including streamsides and drainage ditches. Being a hybrid, it is usually sterile, producing no seeds and reproducing only vegetatively, spreading by its runners.

In perfumery, peppermint oil interacts well with cedar, basil, bergamot, lime, marjoram, pine, rosemary, mandarin, and thyme. Very intense and more concentrated than most other steam-distilled essential oils, it is quite versatile as a middle note in fragrances, providing richness. At lower dilutions, it blends especially well with grapefruit and lemon top notes and lavender and eucalyptus middle notes.

In addition to its use in perfumery, peppermint has a variety of other applications. Fresh or dried peppermint leaves are often used alone in peppermint tea or with other herbs in teas (tisanes, infusions). Peppermint is used for flavouring ice cream, candy, fruit preserves, alcoholic beverages, chewing gum, and toothpaste, and as an odorant in some shampoos, soaps and skin care products.

Dried peppermint leaves have been found in Egyptian pyramids dating to 1000 BCE. Although it has been used in folk medicine for thousands of years for minor ailments (including topical use for muscle/nerve/joint pain or for itching), medicinal uses of peppermint have not yet been approved as effective or safe by the US Food and Drug Administration. With caution that the concentration of the peppermint constituent pulegone should not exceed 1% (140 mg), peppermint preparations are considered safe by the European Medicines Agency when used in topical formulations for adult subjects. Diluted peppermint essential oil is thought to be safe for oral intake so long as only a few drops are used. In this way, peppermint is commonly used as a digestive aid and for stomach complaints, headaches, respiratory symptoms, and nervous system disorders, and it is reputed to help concentration and focus. Although some have used peppermint oil for morning sickness, the oil has not been approved for use in pregnancy.

Although peppermint is commonly available as an herbal supplement, there are no established, consistent manufacturing standards for it, and some peppermint products may be contaminated with toxic metals or other substituted compounds. Skin rashes, irritation, or an allergic reaction may result from applying peppermint oil to the skin, and its use on the face or chest of young children may cause side effects if the oil menthol is inhaled. A common side effect from oral intake of high doses of peppermint oil is heartburn. Oral use of peppermint products may have adverse effects when used with iron supplements, cyclosporine, medicines for heart conditions or high blood pressure, or medicines to decrease stomach acid. The oil is undergoing preliminary research for its potential as a short-term treatment for irritable bowel syndrome. In high concentrations, ingested peppermint oil can cause abortions and should not be used by pregnant women.

Peppermint flowers provide nectar for organisms such as honeybees, but the plant's oil has a high concentration of natural pesticides, mainly pulegone and menthone, and is known to repel some pest insects such as mosquitos.

A less common peppermint chemotype is lemon mint or bergamot mint (Mentha citrata Ehrh). Its essential oil has a smell recalling lavender and bergamot, and it contains almost no menthol. This oil is rarely used in perfumery since it is much more expensive than bergamot and lavender oils.
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Another important species in the genus is spearmint (Mentha spicata, from the Latin 'bearing a spike,' or Mentha viridis), which is actually a hybrid of horse mint (Mentha longifolia or Mentha silvestris) and round-leaved mint (Mentha rotundifolia, itself a hybrid). Spearmint originated in Italy and France. Various types of spearmint are cultivated now in the U.S., Great Britain, Germany, and Japan. It is a perennial herbaceous plant, 30–100 cm tall, with variably hairless to hairy stems and foliage and a wide-spreading fleshy underground rhizome from which it grows. The leaves have a serrated margin, and the stem is square-shaped. Spearmint produces flowers in slender spikes, each flower pink or white in colour. Spearmint blooms in the summer (from July to September in the northern hemisphere).
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Mentha spicata was first described scientifically by Linnaeus in 1753. It is indigenous to the eastern Mediterranean, from Italy to Egypt. Mention of spearmint dates back to at least the 1st century AD, with description by the naturalist Pliny and references in the Bible. Ancient mythology also has descriptions of mint, including spearmint. It was introduced into England through the Romans by the 5th century, and early versions of toothpaste using mint in the 14th century suggest widespread domestication by that point. John Gerard's Herbal (1597) states that: "It is good against watering eyes and all manner of break outs on the head and sores. It is applied with salt to the biting of mad dogs," and "They lay it on the stinging of wasps and bees with good success." He also mentions that "the smell rejoice the heart of man, for which cause they used to strew it in chambers and places of recreation, pleasure and repose, where feasts and banquets are made." Spearmint is documented as being an important cash crop in Connecticut during the time of the American Revolution, at which time mint teas were popular because they were not taxed.

Chemically, spearmint essential oil is quite different from peppermint oil, with the major aromatic component being L-carvone, and menthol and menthone generally not exceeding 1%. L-carvone has a sweet minty smell, while its mirror enantiomer D-carvon (a main component of caraway essential oil) smells spicy and harsh. Spearmint oil also contains significant amounts of limonene, dihydrocarvone, 1,8-cineol, and carvyl acetate. Unlike oil of peppermint, oil of spearmint contains minimal amounts of menthol and menthone.

Unlike peppermint oil, spearmint oil has had few specific medical uses, but it has been used some in traditional medicines for minor ailments such as fevers and digestive disorders. It is widely used as a flavoring in toothpastes and chewing gums and to add aroma to shampoos and soaps. Spearmint leaves are infused in water to make spearmint tea, and it is an ingredient of the famous Moroccan Maghrebi mint tea. Spearmint is an ingredient in several mixed drinks, such as the mojito and mint julep. Sweet tea, iced and flavoured with spearmint leaves, is a summer tradition in the southern United States.

Spearmint essential oil has had some success as a larvicide against mosquitoes. Using spearmint as a larvicide is reputed to be a 'greener' alternative to synthetic insecticides due to the latter's toxicity and adverse environmental effects. Used as a fumigant, spearmint essential oil is an effective insecticide against adult moths.

Another common but less widely used mint species is corn mint (lat. Mentha arvensis L.), with several chemotypes whose essential oils mainly are used for menthol. A final plant classically similar to mint is geranium, due to the presence of menthone. Mint and geranium can be found combined in Frédéric Malle Géranium pour Monsieur, a scent said to be inspired by traditional fragrant Moroccan soap.


Menthol Crystals or Flakes

Menthol (a terpene alcohol, commonly called mint camphor or peppermint camphor) is an organic compound made synthetically or obtained from the oils of mints. It is a waxy, crystalline substance, clear or white in color, solid at room temperature and melting slightly above that. Naturally occurring menthol (l-menthol) is the l-rotatory enantiomer, while synthetic menthol is racemic, consisting of equal amounts of both enantiomers.

Peppermint and wild mint (Mentha arvensis), primarily grown in the Uttar Pradesh region of India, are the primary species of mint used to make natural menthol crystals and flakes. The crystals are obtained by freezing and then filtering the essential oil. Menthol flakes are crystals reduced to a powder. India and China are the largest producers of the world's natural menthol.
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It is said to have been known to the Japanese for more than 2000 years. In the West, menthol was first isolated chemically in 1771 by Hieronymus David Gaubius. It was named in 1861 by F.L. Alphons Oppenheim.

Stimulating the cold-sensitive TRPM8 receptors in the skin and mucosa, menthol causes the cooling sensation when it is inhaled, eaten, or applied topically (similar to the heat-sensor effect of capsaicin, the chemical responsible for the spiciness of chili peppers). It has a characteristic 'cold' smell, transparent and clean, with camphoric, green, and spicy tones. The corresponding ketone, menthone, has a minty smell with much brighter, herbal-green, anisic effects. In perfumery, menthol primarily is used to prepare menthyl esters, which emphasizer floral notes (especially rose) in fragrances. In perfumes and cosmetics, it has some disadvantages: it is quite volatile; has a verybright smell that is difficut to fit into aromatic compositions; has a bitter taste; and in higher concentrations, provokes a sensation of burning. Chemical investigations of menthol and similar 'cooling' materials have been conducted for almost a century, and about 1200 new entities have been synthesized, some more cooling than menthol, less volatile, and not bitter tasting. But few of them have been used yet in perfumery.

Menthol is included in many consumer products, including:
-nonprescription lip balms, cough medicines, and relievers of sore throat and minor mouth or throat irritation
-antipruritics
-topical analgesics, sometimes combined with camphor, eucalyptus oil, or capsaicin
-patches to reduce children's fevers
-transdermal drugs (as a penetration enhancer)
-decongestants for chest and sinuses (cream, patch, or nasal inhaler)
-sunburn medications (often associated with aloe)
-first aid products such as 'mineral ice' to produce a cooling effect as a substitute for ice in the absence of water
-aftershave products
-some cigarettes, for flavor and to reduce mucosal irritation (and also increasing nicotine addictive potential)
-oral hygiene products and bad breath remedies
-chewing gum and candy
-beauty products such as hair conditioners

Menthol's analgesic and counterirritant properties are mediated through selective weak activation of dermal agonist kappa-opioid receptors and blockage of voltage-sensitive sodium channels, which reduces neural activity. Studies show that it acts as a GABA receptor-positive modulator. Its anesthetic properties are similar to those of propofol. In 2017 it was the 193rd most commonly prescribed medication in the U.S., with more than 2 million prescriptions. It has been used in upper gastrointestinal endoscopy as an antispasmodic and smooth muscle relaxant. Menthol is used in dental care as a topical antibacterial agent, effective against several types of streptococci and lactobacilli.

It is used as a pesticide against tracheal mites of honey bees.

Most mint fragrances are deemed unisex, but some are somewhat sharper and aimed more toward men.

'Masculine' Fragrances with Mint or Menthol:

Abercrombie & Fitch 1892 Yellow
Al-Rehab Romantic
Altika Yves Rocher
Alt-Innsbruck Eau de Cologne
Amouage Beach Hut Man
Annick Goutal Eau de Monsieur
Aramis Surface
Armani Code Sport Giorgio
Avon Prime, Real, Musk Marine
Axe Shock, Black Chill
Azzaro pour Homme Wild Mint, Aqua
Barbasol Brisk, Pacific Rush
Battistoni Marte Red Planet, Marte 61
Calvin Klein Crave
Cartier Roadster
Chanel Bleu, Allure Homme Sport Eau Extreme
Creed Royal Mayfair
Davidoff Cool Water (various)
Durance en Provence Fresh Mint
Dzintars Hit Yellow, Lucky No.15
Emper Bandit
Frédéric Malle Géranium pour Monsieur
George F. Trumper Paisley
Givenchy Gentlemen Only Parisian Break
Guerlain Homme (various)
Hugo Boss Mats Hummels, Orange Made for Summer, Iced, Just Different
Humiecki & Graef Eau Radieuse
Issey Miyake Sport Mint
Jean Paul Gaultier Le Male (various)
Jequiti Champs Fort, Merci, l'Attitude Musique
Judith Williams Man No.2
Kanebo Goce
Korres Aktis
Liz Claiborne Curve Wave
l'Occitane Verdon
Marco Serussi White
Massimo Dutti Island Accord
Master Perfumer Grey Fougere No.9
Mennen Skin Bracer
Milton Lloyd America Sport, Colour Me Blue
Montblanc Legend Special Edition 2014
Mugler Kryptomint, A*Men (various)
Nautica Voyage Heritage, Midnight Voyage
Nickel Ulla Lala
Oriflame Glacier Fire, Eclat Toujours, Free Motion, Venture
Paco Rabanne One Million, Ultraviolet
Phaedon Oriental Mint
Pierre Cardin Signe
Prada Luna Rossa
Proraso Green
Ralph Lauren Big Pony No.3
Ricardo Ramos ZirYab Peppermint
Shirley May Sapphire Man
Versace Eros
Williams Aqua Velva Menthol Mist
Xerjoff Renaissance
Yves Rocher Altika, Eryo Blue, Bois de Cedre et Citron, Comme Une Evidence Green
Yves St. Laurent Live Jazz
Zara Man Silver Winter, 2012
 
Aromatic Extraction Techniques in Perfumery

Before perfumed products can be composed, the odorants used in the various perfume compositions must first be obtained. Synthetic odorants are produced through organic synthesis. The term "aroma extraction" refers to the extraction of aromatic compounds from raw natural plant materials, using methods such as distillation, solvent extraction, expression, or enfleurage. The results of the extraction are essential oils, absolutes, concretes, or butters, depending on the amount of waxes in the extracted product. The different methods have been devised to make the extracted material smell as much like the donor plant as possible and to be cost-effective. To a certain extent all of these procedures are damaging: they denature the aromatic compounds, changing their odor profile or even making them totally odorless. This has to do with the materials themselves having so little volatile oil that they do not yield a sufficient crop (lily of the valley and gardenia, for example) or being too delicate to withstand techniques that employ heat, harsh solvents, or exposure to oxygen.

Commercial Extraction Processes

EXPRESSION

Expression is among the oldest methods of fragrance extraction. Aromatic essential oil is produced from plants that are squeezed or compressed, forcing the complete oil out. These oils were first produced in Egypt in unglazed ceramic vases, with the flowers pressed and then buried in the desert for driving out the moisture. The water has a smaller molecular size, so it diffuses through the ceramic vessels, while the larger essential oils do not. The lotus oil in Tutankhamen's tomb, which retained its scent after 3000 years sealed in alabaster vessels, was pressed in this manner. Expression is an especially mild process, historically used in cases where steam distillation would modify or damage the end product. Today the only oils obtained by expression are those from the rinds of citrus fruits, due both to the abundance of aromatics in this squeezable part of the fruit and to the low cost of growing citrus fruits in general. This method is sometimes called cold pressure extraction.


DISTILLATION

Distillation, using an alembic (an alchemical still consisting of two vessels connected by a tube), is an advanced method developed in the Middle Ages and is now a common one, used for rendering a variety of aromatic essences, with the raw material sources being wood, bark, roots, flowers, leaves, seeds, peels, and flowers. In this procedure, a carrier solvent (usually water but sometimes another liquid such as alcohol) is boiled and its steam is passed through the raw material in the still for 60-100 minutes, taking the fragrant substances along with it. After cooling and condensing of the vapor, the essential oil, which floats to the top, is separated from the distillation water in Florentine flasks. The resulting material is still mostly called an essential oil, comprising aromatic and volatile ingredients of the raw material. Several very common essential oils such as peppermint, basil, lavender, rose, palmarosa, geranium, sandalwood, and eucalyptus, are produced in this way. Distillation produces different quality grades of essential oils, making some finer than others. The water collected from the condensate, which retains some of the fragrant compounds from the raw material after the oil is removed, is called hydrosol and is also sometimes sold. Examples are rose hydrosols and orange blossom hydrosols.

Rectification (also called dry or destructive distillation): The raw materials are directly heated in a still, without a carrier solvent such as water or alcohol, and often in the absence of air. Fragrant compounds that are released from the raw material by the high heat undergo anhydrous pyrolysis, which results in the formation of different compounds and thus different fragrance notes that can be used in perfume compositions. This method is used to obtain fragrant compounds from fossil amber and fragrant woods, where an intentional "burned" or "toasted" phenolic (tar-like) odor is desired. Examples are birch tar oil and Styrax pyrogenated oil.

Fractional distillation: A prolonged process is used, employing a fractionating column, which renders several grades of the aromatic compound, varying in quality and depth of scent. This allows for greater control of the qualities of the end material produced and is therefore very helpful in allowing manipulation of the effects they have in a fragrance formula. Although the product of fractional distillation is more expensive, this process is sometimes necessary to remove unpleasant or undesirable scents of a material. It is commonly used for ylang-ylang.


SOLVENT EXTRACTION/MACERATION

Organic solvent extraction is the most common and most economically important technique for extracting aromatics in the modern perfume industry. Raw materials are submerged in a solvent that can dissolve the desired aromatic compounds. Commonly used solvents for maceration/solvent extraction include hexane, ethane, and dimethyl ether.

Fragrant compounds from woody and fibrous plant materials are often obtained in this way, as are all aromatics from animal sources (although this is increasingly uncommon due to ethical concerns). The technique can also be used to extract odorants that are too volatile for distillation or are easily denatured by heat. The remaining waxy mass is known as a concrete, which is a mixture of essential oil, waxes, resins, and other lipophilic (oil-soluble) plant material. Although highly fragrant, concretes are too viscous - sometimes even solid - at room temperature to be useful. This is due to the presence of high-molecular-weight, nonfragrant waxes and resins. Another solvent, often ethanol (ethyl alcohol), which only dissolves the fragrant low-molecular-weight compounds, must be used to extract the fragrant oil from the concrete. The alcohol is removed by a second distillation, leaving behind what is called the absolute. Due to the lower temperatures used in this process, the absolute can be more faithful to the original scent of the raw material than are the products of distillation.

To differentiate between an absolute and a tincture: A tincture is a material produced through use of ethanol extraction directly from dry materials submerged in the alcohol, while absolutes are rendered through washing and effectively purifying with ethanol the waxy materials (oils, concretes) derived from solvent extraction/enfleurage.

Supercritical fluid extraction: In supercritical fluid extraction, a relatively new method, high pressure carbon dioxide gas (up to 100 atm) is used as a solvent. When carbon dioxide is put under high pressure at slightly above room temperature, a supercritical fluid forms. (Under normal pressure, CO2 changes directly from a solid to a gas in a process known as sublimation.) CO2 in a non-polar compound has low surface tension and wets easily, and it can be used to extract the typically hydrophobic aromatics from the plant material. This process is identical to one of the techniques for making decaffeinated coffee. Like solvent extraction, CO2 extraction takes place at a low temperature, extracts a wide range of compounds, and leaves the aromatics unaltered by heat, producing an essence that is very faithful to the original. Since CO2 is a gas at normal atmospheric pressure, it also leaves no trace of itself in the final product, thus allowing one to get the absolute directly without having to deal with a concrete. Extracts produced using this process are known as CO2 extracts.


INFUSION

Water maceration produces an infusion, a familiar term from tisanes/herbal teas and a comparable technique. The plant material is submerged in hot water (or alcohol or oil) and left to marinate (steep) for a period of time, yielding its aromatic properties. Then the plant is removed with a strainer and the water remaining is called an infusion. The process of infusion is distinct from decoction, which involves boiling the plant material, or percolation, in which the water passes through the material (as in a coffeemaker). Infusion is a very simple chemical process used with botanicals that are highly volatile and dissolve readily or release their active ingredients easily in the liquid. The botanicals are typically dried herbs, flowers or berries.


DECOCTION

Decoction is a method of extraction by boiling out dissolved chemicals from mashed plant material, which may include stems, roots, bark, and rhizomes. Decoction produces liquids with differing chemical properties than those of infusion because the temperature/preparation difference results in more oil-soluble chemicals in decoction than in infusion. Decoction is also the name for the resulting liquid.


ENFLEURAGE

Enfleurage is a famous but now antiquated process, prized in years past for its capacity to capture the mature, deep aroma of delicate flowers, such as jasmine or tuberose, that lost their precious aromatic bouquet in high-heat distillation. Enfleurage in the original French means to “impregnate with the scent of flowers.” It is also defined as “extracting perfumes by exposing inodorous oils or fats to the exhalations of flowers.”

The technique uses animal fat (deodorized lard or tallow) as a waxy 'dress' for the flowers, allowing them to macerate for days on large glass plates in wooden frames. Fresh produce was added to the point of fragrance saturation. The fragrant fat 'pomade' was then washed with ethanol to render an 'absolute de chassis.' Two variations of the technique existed: 'cold' enfleurage, perfected in the 19th century and using no external heat, and 'hot' enfleurage, in which the fat was gently heated while the botanical matter was stirred into the fat.

This technique is not commonly used any longer in the perfume industry, due both to its prohibitive labor intensity and cost and to the existence of newer, more efficient extraction methods such as solvent extract and supercritical fluid extraction.


Otto, Attar, and Monoi

Otto (most often rose otto, but also including saffron, lotus, and jasmine osttos) is essential oil derived from the petals of flowers. Rose otto is produced from different varieties of roses through steam distillation (as opposed to the absolute, which is produced through solvent extraction or supercritical CO2 extraction). The finest rose otto is produced in Turkey and Bulgaria. Ottos are used less often in perfumery than absolutes.

Attar is the English form of the Arab term ittar, an ancient Persian word meaning "to smell sweet." It is used to denote a variety of natural oils rendered from botanical sources, especially those that do not contain any added alcohol. The oils are most often distilled into a wood base such as sandalwood and then aged. The aging period can last from one to ten years depending on the botanicals used and the results desired. Attars are highly concentrated and therefore are usually offered for sale in small quantities in decorated crystal cut bottles or small jeweled decanters. The terms attar and otto are sometimes use interchangeably.

A variation on this is the famous Monoi ("scented") oil, which uses Tiaré flowers (i.e. Tahitian gardenias), macerated and distilled in coconut oil (which is a semi-solid wax substance in its pure form).
 
Soapiness

What is called a soapy fragrance also is frequently termed 'fresh, clean, and watery.' When the term 'soapy' is used, it usually means the scents associated with perfumes commonly added to soaps. Fragrance pyramids generally do not mention a soapy scent, although it is present in many compositions. Soapy fragrances generally are thought to constitute a subdivision of 'fresh' scents in classification schemes. The connection between soap and perfume is not really found in the various aromas they may share, but in the message that they both can broadcast: "I am clean."
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Soapy scents are described as somewhat crisp, sometimes slightly cooling, and slightly pungent in a pleasant way, but also creamy and relatively mild. The concept of a soapy smell varies from person to person, depending upon where they grew up, which soap they habitually use (or used in childhood), and what fragrance (often primarily artificial) was added to that memorable soap.
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Generally one can say that a soapy fragrance evokes the scent of freshly used shower soap, and it is meant to prolong the feeling of just having come out of the shower. Plain soap by itself usually has almost no discernable scent, although there may be a hint of residual unsaponified fat. Adding fragrance to soap is a relatively modern phenomenon, only appearing after the Industrial Revolution and commercialization of soap manufacture. Cashmere Bouquet of the late 1800s is thought by some to have been the first scented soap.
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Soapy Notes

Many different elements can contribute to a product's soapy quality: extracts of plants or flowers (especially when used soliflore), certain aroma chemicals, or combinations. Some of the most common notes in soapy compositions are green notes and citrus notes, either on their own or mixed together. Fragrances known for this note use include Drakkar Noir and Kouros. Other notes frequently contributing include woods (especially cedar, sandalwood, and pine), aquatics, certain types of musk, unobtrusive florals such as lavender, tobacco, almond, aloe, mint, vetiver, non-citrus fruits, and light spices. Synthetic aroma chemicals are present in most product but sometimes seem to work against the natural tones, producing a somewhat 'fake' vibe, although still smelling good in a generic, my-body-is-fresh way.
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Masculine soaps often have brought the scent of lavender, especially when combined with neroli and/or sandalwood, and this has carried over to masculine fragrances. Linalool, abundant in lavender, smells soapy to 25-30% of the population (but flowery and citrusy to everyone else).
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Lily-of-the-valley, with its floral-green and fresh facets, is another one often interpreted as soapy, although it often is more suggestive of laundry detergent. Other notes commonly used in soaps, such as rose, jasmine, iris, citruses, juniper, ginger, verbena, and abstract 'green' accords, also give a soap impression to fragrance compositions. A common characteristic of these notes is that they all blend with other notes quite easily and smoothly, without much separation. (This contrasts with the presence in perfume products of indoles, animalic notes, and wood tones, which generally prevent a composition from smelling 'clean' unless appearing just transiently in the top notes.) Examples of these blending notes are the rose in l'Occitane Eau de Quatre Reines and Patou Joy and the lily-of-the-valley in Creed Original Vetiver. Citrus and/or blackberry are frequently used, such as in Mugler Cologne, Prada Infusion de Fleurs d'Oranger, and Maitre Parfumeur Eau de Gantier.

Musk, also often used in detergents, can smell especially soapy when paired with citrus or rose because this was exactly the smell of classic soaps of decades ago, such as Camay, Pears, Dove, and Lux, which frequently were rich in essential oils. They had a basic alkaline smell that was both bitter and sweet, with a vague floral quality.
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Ivory soap is thought to smell the way it does because of a combination of lemongrass and carnation; Dove has synthetic irones (akin to iris) that create a smooth, delicate scent.
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A more modern example of musk use for this is Jennifer Lopez Glow, which was heavily advertised from 2000 as giving a 'just out of the shower' smell. And men's products have been advertised as giving a 'shower fresh' competitive edge in the company boardroom, such as the promotions of Gendarme Carriere, Paco Rabanne Pour Homme, and Mark Pure.

Soapy Aroma Chemicals

Aliphatic or 'fatty' aldehydes have scents ranging from metallic, floral, waxy, or starchy to green or citrus. They all have the common property of having a dominant somewhat 'soapy' aspect to their smell, associated with abstract cleanliness or the lemony scent of freshly ironed linens. One example is 2-methylundecanal, which is a major odor component of Chanel No.5. Aldehydes, discovered in the late 19th century, were first used in perfumes with Houbigant Fougère Royale in 1882 but only became really popular after the huge commercial success of Chanel No.5. Coco Chanel had asked her parfumeur Ernest Beaux for a perfume that 'smells like a woman and not a rose bed,' and he created the aldehydic citrus-soapy No. 5.
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Another aldehyde commonly used is decanal, which has a sweet, flowery scent reminiscent of orange peel. Because of their low price, intensity of smell, and ability to mask the unpleasant base odor of a soap, aldehydes have been heavily used in soapy perfumes for a long time. Well-known products scented by them have included Estée Lauder White Linen and Hermès Caleche. Nevertheless, aldehydic itself does not necessarily equate to 'soapy;' some aldehydic fragrances (e.g. Piguet Baghari, Rive Gauche, Revillon Detchema, Bill Blass Nude) have hints of soapiness but do not immediately evoke a sense of bath soap the way that others do.

Soapy Fragrances

A popular fragrance that typifies the soapy smell is Issey Miyake's 1992 l'Eau d'Issey and its several varieties. Categorized as a floral aquatic, its main accords are white floral, aquatic, ozonic, fresh, and rose. Says the website Fragrantica, "Issey Miyaké thought about creating a perfume that was 'as clear as spring water,' combining the spray of a waterfall, the fragrance of flowers, and the scent of springtime forest. L’Eau d’Issey achieved an enormous popularity, especially in the United States in the 1990s. L’Eau d’Issey is an aquatic floral scent with transparent notes of lotus, freesia and cyclamen and juicy melon. The middle note of peony, lily and carnation reveals the perfume’s character. The end note is a refined woody scent with the notes of cedar, sandal, musk and amber."
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This fragrance apparently influenced Giorgio Armani to produce Acqua Di Giò, which many have described as smelling like clean laundry (while others have said it actually smells like laundry detergent or fabric softener). Subsequent somewhat soapy perfume products have included Kenzo l'Eau, Bvlgari Omnia Crystalline, Calvin Klein Eternity Aqua, Davidoff Cool Water, Gucci Flora Eau Fraiche, and Hermès Jardins en Méditerranée.
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All of this has been promoted, of course, by soap advertisements, which have both reflected our culture (connotations of cleanliness being next to godliness, good complexion care, preservation of youthfulness, and general well-being) and created it. In our modern somewhat germ-phobic social environment, soapy scents seem to represent the solace of cleanliness amidst all the pollution, a form of 'olfactory safety bubble,' as well as a safe, neutral choice for more gender-neutral office workplaces. In addition, a soap smell hinted in the past at high social status, suggesting that the wearer could afford daily baths with hot water and had a refined taste for delicate smells. This concept was suggested in the movie 'Scent of a Woman,' in which the smell of fictional Ogilvy Sisters Soap on the character played by Gabrielle Anwar was admired by the protagonists.
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Masculine fragrances are soapy more often than feminine ones, possibly because women are more hesitant about having their personal wash habits suggested, while men are less shy about communicating that they take washing seriously, especially following their culturally typical rugged, dirty activities.

It can be difficult at first for men to learn what type of cologne to wear for a particular occasion. Soapy fragrances are inoffensive, versatile, and easy to wear year round, and they are usually one of the first types of cologne that a man uses. Many grooming products for men, including aftershaves, soaps, and shampoos, and shower gels, have a clean and fresh scent, so men become accustomed to it. These products often seek to enhance that clean feeling, consciously embodying fragrance profiles resembling 'men's' bath soaps like Zest, Dial, and Irish Spring. A clear example is Sung Homme, which conveys the smell of original Irish Spring soap.
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Some experts and consumers complain about fragrances smelling too much like soap, some even having names like Pure Soap or Laundromat (from Demeter) or Clean Warm Cotton, Fresh Laundry, Shower Fresh, and Lather Clean. They wonder why anyone would want to spend $50-70 or more on a bottle of something just to smell like a fresh shower. They often express preferences for more complex compositions with a suggestion of soapiness, but with other notes or accords to enrich them and make them more interesting.
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A general consensus is that soapy perfumes generally are best worn during the warmer summer months, when feeling clean and fresh is most important, especially for casual events. However, their versatility also lends them to use for formal occasions and during other seasons.

'Soapy' fragrances for men (* indicating general consensus ones):

Acqua di Parma Essenza
Alfred Sung Sung Homme
Al Haramain Neroli Canvas
Amouage Dia, Amouage Reflection Man
Armani Acqua Di Giò
Azzaro Chrome
Bentley
Bijan Nude
Bruno Acampora Musc
Bvlgari Eau Parfumee au The Vert
Burberry Mr. Burberry Indigo, Burberry Touch
Calvin Klein Eternity, CK Euphoria, CK Free, CK One*
Chanel Allure, Chanel Platinum Egoiste
Chrome
Creed Original Vetiver*, Original Tabarome
Davidoff Cool Water
Demeter Pure Soap
Dolce & Gabbana*, D&G Intenso
Dunhill Century
Francis Kurkdjian Lumiere Noire
Geoffrey Beene Grey Flannel
Giorgio Armani Acqua di Giò
Guess 1981 Indigo
Guerlain Vetiver
Issey Miyake l'Eau d'Issey*
Jean Paul Gaultier Le Male
Jil Sander Sun
Miller & Beerteaux Spiritus
Mont Blanc Individuel
Narciso Rodriguez
Nautica Voyage
l'Occitane en Provence l'Occitan
Paco Rabanne Pour Homme*
Penhaligon's Castile
Prada Amber*, Prada l'Homme*, Prada Infusion d'Homme*, Prada Luna Rossa, Prada No4 Fleurs d'Oranger
Ralph Lauren Polo Sport
Rochas Eau de Rochas
Roger & Gallet Open*
Salvatore Ferragamo Acqua Essenziale, SF Subtil
Santa Maria Novella Gold Musk
Serge Lutens Gris Clair
SHL Panthea Iris
Taylor of Old Bond Street Sandalwood
Thierry Mugler Cologne*
Tom Ford Grey Vetiver, TF Neroli Portofino*
Versace Man Eau Fraiche
Yves St. Laurent Kouros, YSL Rive Gauche
 
Melon

Melon is a trailing vine (and its edible fleshy fruit) that originated in Africa and southwest Asia, thought to be current Iran and India. The plants are in the genus Cucumis melo, in the same gourd family (Cucurbitaceae) as squashes and cucumbers. They have large round or lobed leaves and yellow 1-inch flowers. Unlike their cousins the squashes, they are classified as fruits.
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The name melon derives from a Latinized Greek word that combines meanings of 'apple, treefruit' and 'gourd.' Melons are known to have been grown in ancient Egypt, and the plants were brought to Europe by the Nuragic civilization of Sardinia during the Bronze Age (1350-1120 BC), becoming common there by the end of the Western Roman Empire around 476. They were among the earliest plants to be domesticated and among the first crop species brought by the Spanish and Portuguese to the Americas; Christopher Columbus first introduced cantaloupes to the New World on his second voyage there in 1494. And honeydew and casaba melons are recorded as being grown in North and South America by the 1600s.
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Seven distinct cultivar groups of melons are recognized:
1. Reticulatus - Netted or 'musk melon,' having a net-ribbed rind and sweet orange flesh. The most popular cultivated melon. Melons sold in the US as cantaloupes are often the netted melon type rather than true cantaloupes. The W. Atlee Burpee Company developed and introduced the 'Netted Gem' in 1881.
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2. Cantalupensis - True cantaloupes, characterized by a rough, warty rind and sweet orange flesh. Named for Cantalupo, Italy, where they were the first grown in Europe from Asian stock. They are not grown commercially in North America. Pope Paul II became obsessed with cantaloupes during his reign and is said to have eaten 'two good big melons' in one sitting in 1471 and then died. Pope Innocent XIII (1721-24) is reputed to have sipped Port wine from a partially hollowed cantaloupe as an apéritif.
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3. Inodorus - Winter melons, large, smooth-skinned, with mildly flavored light green or white flesh. They include the honeydew, casaba, and Persian melons. The honeydew melon was introduced to China by American Secretary of Agriculture Henry A. Wallace around 1944, when he donated seeds to local farmers during a visit there.
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4. Flexuosus - Snake (or serpent) melon or 'Armenian cucumber,' only 7cm (3 in) in diameter but up to 1m (3 ft) in length, with very thin light green skin and slightly acidic, cucumber-like flesh. It is thought to have been grown year-round for Emperor Tiberius of 1st century Rome.
5. Conomon - Asian common or pickling melons, with smooth skin and greenish flesh that is nonsweet and bland or slightly tart. They are used in Asian cuisines, especially those of Japan and Korea.
6. Chito - Mango-melons, a hybrid fruit, the size and shape of a lemon or orange, with white cucumber-like flesh.
7. Dudaim - 'Stinking' melons (called this because of the foul-smelling vine), the size of an orange and highly fragrant, considered inedible by some.

Only the first three of these cultivars are used in perfumery.

Botanically, melon fruits are a type of berry known as a 'pepo.' They vary greatly in size, shape, surface texture, and flesh color and flavor, depending on the variety, but all have thick firm flesh and an inner seed-filled midsection. They weigh 1-4kg (2-9 lbs). Generally the flavor and aroma are musky or sweet or both.
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In 2018, world production of melons was 27 million tons, led by China with 46% of the total. Turkey, Iran, and Indian produced more than 1 million tons each. Most commercially important melons are eaten fresh, although some varieties can be pickled or made into preserves.
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Melons in Perfumery
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To date it has not been possible to extract melon essential oil from the fruits. In perfumery, melon is a fresh, green, sweet, fruity, somewhat metallic marine/aquatic note that is usually produced by Calone® (methyl benzodioxepinone), a lab synthetic that became very popular in the 1990s, most often combined with touches of other notes (such as caramel) to provide spice or fullness. Calone® was first synthesized in 1951 by chemists from Camilli, Albert & Laloue, precursor of Pfizer, who were looking for an affordable tranquilizer. The lab policy then was to name all compounds according to a code that included the first letters of the company (CAL) and the chemical class (ketone), thus giving Calone. It was patented in 1966 and was used over the next 20 years as a marginal perfume ingredient, mainly in trace amounts for flower accords. Only after the patent expired in the late 1980s did it enter its glory era, first with Aramis New West. Other companies quickly began to produce and use it, and it now is known by many other names, including Aquamore, Watermelon Ketone, Ozonor, and Ozeone. It is similar in structure to brown algae pheromones and is related in structure to the benzodiazepine class of sedatives.
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Another popular melon synthetic is Givaudan Calypsone, which smells ozonic, like a sea breeze, with underlying fruity watermelon nuances. Calypsone has been used in Avon Exclusive in Black, Azzaro Wild Mint, Calvin Klein Summer Daze, Elizabeth Arden Curve Appeal, and Kenzo Homme.

Usually put in the fruity family, melon notes bring cheerfulness and depth to fragrances. Traditionally, fruity notes were mostly employed in feminine fragrances, but subsequently masculine products have contained increasing amounts of fruity scents, including melon once again, especially in the niche side of the fragrance market. One house that is especially notable for using melon is Hermès, which may be related to the fact that it has a 45% share of the Asian market, where tastes show a strong preference for lighter, fresher scents. In addition to the synthetic scents, perfume compositions have occasionally used actual juice extracted from the fruits themselves, starting in the 1920s with the use of those from watermelon, cantaloupe, and honeydew in perfumes from Coudray, d'Orsay, and Dior, and more recently in products from Liz Claiborne and Aramis.
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In addition to the proprietorial synthetics, lab aromatics that have been used frequently to give melon suggestions to fragrances include esters, sesquiterpenes, norisoprenes, short-chain alcohols, aldehydes, and various sulfur-containing compounds, all derived from headspace technology studies of melons, especially watermelon. The one most often used is the 'melon aldehyde' (2,6-dimethyl-5-heptenal). There are now synthetics that are commonly used to specifically mimic cantaloupe, watermelon, and honeydew melon.

Typical melon examples of the 1990s include Issey Miyake l'Eau d'Issey for Men, Davidoff Cool Water, Ralph Lauren Polo Sport, Armani Acqua di Gio, and Calvin Klein Escape. Grooming and cleansing products of that time increasingly used fruit scents to get away from the overboard opulence of the 1980s, and melon and peach were often used for influencing consumers to buy products that did not cost much to produce. By distancing themselves from the herbal scents of the 1970s and the heavy early-1980s shampoos, the new generation embraced fruity notes as a symbol of the upbeat joyfulness of a shower or salon experience. Eventually, however, this got to be too much, and overall sales of melon-based scents dwindled for awhile, with buyers despising them as too mundane and many perfumes being reformulated to decrease or even remove their 'marine freshness.'
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However, more recently there has been a resurgence of interest in melon notes, perhaps just reflecting the cyclical nature of fragrances. In 2007 alone, Bond No.9 premiered its Coney Island, Missoni launched Acqua, and Estée Lauder included cantaloupe in some of their flanker products. And sales of some of the classic melon fragrances from decades ago have remained steady.

Like other fruity notes, melon has been associated frequently with those of the citrus, chypre, and oriental fragrance families. For example, it frequently is orchestrated in a fresh and subtle way, without additional sweetness, to accompany citrus fruits or fresh floral notes or to highlight a gourmand tone. Depending on the combinations, melon can highlight refinement and delicacy or it can reveal a playful, child-like side. It acts right from the start of the volatile top notes but mainly is present in the heart notes, often presenting a light prelude for later, darker aspects of a formula. In contrast, melon - especially crisp honeydew - often sets the tone in predominantly aquatic and salty ocean compositions. Other notes with which melon blends especially well include cucumber, patchouli, and amber.


Male melon fragrances:

1907 Cedar Blue
Abercrombie & Fitch Crest, A&F First Instinct
Adidas Game Spirit
Antonio Banderas Blue Seduction
Avon My Vibe
Bath & Body Works Cucumber Melon
bench An Urban Original 2, bench Sound
Benetton Blue, Benetton Cumbia Colors
Bi-es Ego Platinum, Bi-es Feel OK
Burberry Weekend
Calvin Klein Escape, CK Eternity Summer 2012, CK Reveal
Cartier Pasha Édition Noire Sport
Chanel Bleu
Christian Dior Higher Energy
Christine Lavoisier Parfums Fusion Very Masculine
Contém 1g 81
David Beckham Intense Instinct
David Hechter Contact
Davidoff Good Life
Demeter Honeydew Melon
Exceptional Parfums Because You Are
Ferrari Cedar Essence, Ferrari Essence Musk
Gant Liquid
Hermès Un Jardin Après la Mousson
JohnRichmond
Kenneth Cole Reaction
Liz Claiborne Curve Appeal
Jimmy Choo Man Intense
John Varvatos Vintage
Lomani Lomax Horizon
Louis Varel Reflex Black
Mahogany DSGN
Michael Malul 139 Spice
Nautica Island Voyage
Nike Ion Man
O Boticario Egeo on You
Paolo Gigli Excentrique
Perfumer's Workshop Zipped Apollo
Phebo Guamá
Pierre Bourdon le Grand Tour
Puma Aqua
Ralph Lauren Polo Blue (var.)
Robert Verino VV Man
Rocawear 9 IX
Thera Cosméticos Volcano Gold
Ulric de Varens City Paris, UdV Rectoverso Man Blue Atoll
Uncle Jon's Cucumber Melon
Ungaro Blue Ice
Van Gils Basic Instinct, VG Sport
Zara Classics 8.0, Zara Comme d'Habitude, Zara Denim Couture Red Edition, Zara Summer 8.0
Zirh

Male fragrances designated as honeydew melon:

Al Haramain Entourage Bleu
Bath & Body Works Coconut Mango
Burberry Brit Splash
Calvin Klein Reveal
Cartier Pasha Édition Noire
Clarins Elysium
Francesco Smalto FullChoke
Gallagher Amongst the Waves
Ganache Melones
Gap Blue No. 655, Gap G
Halston
Hermès Le Jardin de Monsieur Li
Jimmy Choo Man Intense
Kansai Yamamoto Éclipse de Soleil
Louis Varel Reflex Black
Michael Malul 139 Spice
Michel Germain Séxūal Secret Man
Nutrimetics Reserved Room
Paris Hilton for Men
Viali VM Challenge


Watermelon

Watermelon (C. lanatus) is trailing vine-like flowering plant (and its fruit) in the Cucurbitaceae family, resembling and related to true melons. It is extensively cultivated and has more than 1,000 varieties. Thought to be native to northeastern Africa, watermelons were domesticated in Egypt by 2000 BC (where they were stored during dry seasons, as both a food source and a method of storing water), and sweet dessert watermelons spread across the Mediterranean world during Roman times. In the 7th century, they were being cultivated in India, and by the 10th century the plants had reached China. The Moors introduced them to the Iberian Peninsula around the same time. The fruit began to appear in European herbal treatises by 1600 and was widely planted in Europe as minor garden crop by the 17th century.
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European colonists and slaves from Africa introduced the watermelon to the New World, with Spanish settlers growing it in Florida by 1576 and the English growing it in Massachusetts by 1629. By 1650 it was being cultivated in Central and South America, and at the same time Native Americans grew it in the Mississippi Valley. Explorers subsequently introduced watermelons to Hawaii and other Pacific islands.

Seedless watermelons were developed in 1939 by Japanese scientists but did not become very popular until disease-resistant hybrids were created in the 21st century, rising to become nearly 85% of total watermelon sales in the US in 2014. Other countries do not use nearly as much of the seedless varieties.
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It is grown now in tropical to temperate regions worldwide, needing temperatures higher than around 25 degrees C (77 F) to thrive. In 2017, China produced two-thirds of the world total watermelon crop.

Watermelon fruit is also a pepo berry, with a hard rind and sweet juicy flesh that varies from deep red to pink and most varieties with many black seeds. It can be eaten raw, juiced, or pickled, and the rind is edible after cooking. Initially the fruit had yellowish-white flesh that was bitter rather than sweet, but the process of commercial breeding allowed production of the current type of fruit. The fruit is over 90% water by weight.

In perfumery, watermelon note overlaps the fresh qualities of the aquatic, green, and fruity families, adding 'sweet wetness' or an illusion of water; but it most often is classified in the fruity group. It sometimes is perceived much like a sliced cucumber or 'ambiguous melon,' the sort of 'ocean air' only found in perfumes and not in reality. It generally has a sweet but obviously synthetic tone. For the most part, what is smelled in perfumery as watermelon in Calone®, sometimes called 'watermelon ketone'. Watermelon note usually smells somewhat sweeter than the more general melon note and has more of a presence in the top notes. Watermelon blends especially well with citrus notes (bergamot, clementine, lemon, mandarin, and grapefruit), other fruity notes (green apple, peach, pineapple, red berries, red current, and pear), and herbs and spices (coriander, basil, bamboo, tea, cardamom, pink pepper, rhubarb, cinnamon, and mint).

Watermelon aroma has been researched extensively, partly because it is notoriously hard to reproduce artificially. In real life, the aroma molecules are produced as a consequence of the fruit being cut open, which releases cellular enzymes that increase the oxidation of fatty acids into aroma compounds. Initial studies suggested that the primary odorants were C6 and C9 alcohols. They were suspected due to their relatively high concentrations. However, they also were found to have higher human odor detection thresholds than some of the other aromatic compounds present; and eventually it was noted that while the researchers collected the compounds over long periods of time, enzymatic action converted their aldehydes into alcohols. It is now thought that the C6 and C9 aldehydes themselves make the main contribution to the fresh watermelon aroma, especially 3,6-nonadienal, which is described in technical literature as 'green fatty dry cucumber violet leaf.' This 'watermelon aldehyde,' a very potent odorant with an estimated detection threshold in water at 0.2 ppb, possesses by itself an aroma very similar to freshly-cut watermelon; unfortunately it is unstable, and working with it is quite difficult. Another one is 3-hexenal, which also is largely responsible for the smell of freshly-cut grass. Attempts to produce esters with a similar structure to these molecules that might provide a similar aroma have been unsuccessful.

Male watermelon fragrances:

12 Parfumeurs Francais le Roi Chanceux
Adidas Fresh Impact
Alan Bray Maxsus Silver
Annayake Love
Antonio Banderas Cocktail Seduction Blue
Avon Blue Rush, Avon Elite Gentleman Reserve
Axe Black, Axe Touch
Baldessarini Ambre Eau Fraiche, Baldessarini Del Mar Seychelles LE
Byblos Uomo 2001
Calvin Klein Eternity Summer 2007, CK Eternity Summer 2014
Carolina Herrera Chic
David Beckham Signature
Davidoff Cool Water Game
Dina Dagger Night
Dunlop Power Elixir
l'Erbolario Felci
Ferrari Black Shine, Ferrari Cedar Essence, Ferrari Essence Musk
Franck Olivier Sun Java
Gianni Versace Metal Jeans
Genty Sniper
Jacques Evard Flyback
Kenneth Cole Reaction
Lacoste L.12.12 Noir
Laura Biagiotti Aqua di Roma
Liz Claiborne Curve Appeal
Mahogany Blue Energy
Mexx Cocktail Summer
Michael Jordan 23
Michael Malul Visionair Midnight Blue
Oriflame True Instinct
Pascal Morabito Mediterranee
Puma Create, Puma Man, Puma Time to Play
Rance Le Vainqueur
RisingWave Eternal
Royal Cosmetic Platinum Air
s.Oliver Casual
Star Wars Rogue One
Tommy Bahama
Versace Metal Jeans
Zara In Tulum
 
Fragrance Layering

Layering, or 'scent mingling,' is the use of more than one fragrance at a time, often as a way to create one's own signature 'bespoke' scent. It is sometimes called 'fragrance cocktailing.' Says perfumer Laurice Rahmé, 'Custom scents capture the personality of an individual. It allows them to whip up their own scent blends whenever the mood suits them.' Although this has been done for centuries, it still is considered a very inexact science, requiring that one be a sort of artist, 'painting with fumes.' The idea generally is to accentuate every note and accord, making them shine more and enhancing their overall intensity, longevity, and sillage. Generally the greater the number of layers, the greater the longevity.

The trend of layering seems to have come initially from the Middle East, where men and women have been mixing fragrances - up to several decadent ones at once - for a very long time (and where some cultures have considered the use of a single scent to be unacceptable). Many Middle Eastern families have a designated 'perfumer' member who does the mixing and layering of scents for everyone in the family.

There are two major schools of thought about layering fragrances. The 'Purist' school, to which many perfumers and reviewers belong, asserts that a fragrance - and especially a classic one - is a thoroughly conceived and finished work and that any changing of it destroys the balance the original creator tried to achieve. The 'Experimentalists,' on the other hand, see a valuable potential in being able to come up with interesting new combinations and to understand smells more completely. They note that one of the best things about layering is that one can comprehend the various 'weights' of notes or accords, sensing which ones disappear first and which ones last longer, which otherwise can seem too theoretical. The idea is that the more we understand fragrances firsthand, the more likely we are to appreciate the most complex commercial compositions available. Experimentalists also like to point out that layering can be cost effective, since one can sometimes use a larger quantity of a less expensive everyday or drugstore perfume as a base, while using a smaller amount of a more expensive product. In this way one can enjoy the creation of a bespoke fragrance without having to pay the high price to a perfumer.

'Layering fragrances is an easy way to get a custom effect,' says Julia Zangrilli, NOVA perfumer. 'The scent is familiar, but not quite - no one else has the exact blend.' Perfumer Alexander Lee says, 'I always saw fragrances to be invisible pieces of clothing. For me fragrance combining is simply wearing multiple fragrances at the same time with the goal to create a personal olfactive form. It's an outlet for the perfume lover to be creative. In fact, a perfume is the result of combining singular perfume notes with other complex accords. Fragrance layering is like walking in the shoes of a perfumer.'

Most experts encourage people to layer initially on a sheet of scent blotting paper, applying the scents one after another without allowing the base to dry. Then when one finds a combination that they like, they can mix it again and apply it to the skin. Says Zangrilli, 'Always test on a piece of paper before trying on your skin, so you aren't always stuck scrubbing off mistakes.' Or rather than using blotting paper, you can do an at-home test by spraying each scent onto a separate cotton ball, pressing them together, then tossing them into a Ziploc bag and sealing it for a few minutes. Then open the bag and smell, and it you like the aroma, try it on your skin. The experts all recommend dabbing or spritzing the scents on a pulse point such as your wrist, and not rubbing, so that they can breathe on your skin. (If a rollerball fragrance is used, it should be applied only to clean, dry skin, so that the smells are not co-mingled on the applicator. If using two products with rollerballs, apply each to a different wrist and then press the wrists together for a moment.)
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One writer recounted a successful experiment of spraying a little of two different fragrances into a new vial, letting them sit for a few days, and then applying them to the skin as if the mix was a new perfume. Since our noses become somewhat insensitive to our fragrances fairly quickly, EO Products perfumer Susan Griffin-Black recommends a challenge: 'One way to test the strength of our scent is to apply the perfume(s) to a piece of cloth. Apply the amount you would normally wear, leave it in a room for a few minutes, and then remove it from the room. Go back into the room after a few more minutes. If you can still smell the fragrance, you've used too much. Your personal scent should only be noticeably strong to someone who is in your personal space (hugging, for instance). Ideally, your scent should only linger for moments after you've left.'

Some say that the safest way to start layering is to use a very common note such as jasmine, rose, or vanilla; to use citrus notes, since they blend easily with floral, woody, and amber scents; or to begin with a light wood note such as sandalwood. Perfumer Patti Kapla says that vanilla and musk are also 'safe' for starting to layer. Zangrilli advises trying very subtle, minimalist fragrances (often those advertising one or two notes in their titles). Another suggestion is to try combining several soliflores (single-flower scents) to create a complex floral perfume. Perfumer Rachel ten Brink says that single-note scents or very light ones are easier to layer. 'Especially heady fragrances - think Chanel No5, Shalimar, and Opium - or evening/noir fragrances - Versace Noir and Tom Ford Black Orchid - are usually too much if combined and may end up giving you a headache.' She also recommends that your total number of spritzes should be no more than the number you usually would spray of just one commercial scent. The linear fragrances from Demeter are perfect for beginners to use for very simple layering. To minimize the cost of experimenting with layers of unfamiliar scents, one can use less expensive mini-bottles.
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Among the different major fragrance groups, those of the floral family seem to be the most foolproof for layering, while those in the oriental family are the trickiest. Also relatively easy to layer are the woody and musk-based scents, since they combine very readily with floral, fruit, or spicy accords. The simplest approach, recommended by some, is to layer only scents in a single family at first. (If one is unsure of the components of a composition, experts note that one can determine the notes present in a given fragrance by putting its name into an online search engine or a fragrance review site such as Fragrantica.com)
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A suggestion from Zangrilli is to separate your scents into two general groups, a Group A of those that are rich in floral or citrus notes and a Group B of those that are aquatic/oceanic, green, or powdery. Then, she says, 'Play with mixing one from A and one from B, or maybe two from A or two from B. You can layer more than two, but this is a good starting point.'
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Addition of scent notes can accentuate a trait in the same olfactory family, such as adding pure vanilla scent to an oriental fragrance that already has some vanilla; or it can strengthen a particular smell character, for example adding patchouli to an oud scent. Linear scents in particular are perfect for beginners to use for layering, since they simplify the process. Zangrilli notes, 'If you want to amplify a single ingredient, jasmine for example, try combining multiple fragrances that feature it as a main note.'
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Some perfumers suggest choosing combinations of very different notes and mixing scents from different families, allowing creation of new fragrances with contrasts, instead of a 'soupy blend.' Examples are mixing a citrus scent with one that is oud-based or a floral perfume with something more intense and sophisticated. Another slightly different approach is to combine fragrances that have different specific memories associated with them, creating a completely new 'dream' experience. Perfumer Carlos Benaim suggests starting with a fragrance with top notes that you love, and pair it with a fragrance that has bases notes you love.
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If one is just beginning, Blanc suggests combining just a spray or two of two fragrances that have a common note or accord and then add from there. Or if one is feeling more adventurous (or just believes that there is little value in mixing scents that are very similar), they can try combining two or more somewhat opposite fragrances - a spice and a vanilla, for instance. Some recommend avoiding the mixing of extreme families, such as oceanics/aquatics with orientals or heavy woods, because they can cancel each other. Benaim says, 'You want to create contrast. The easiest way to do so is to layer lighter fragrances with ones that are a bit heavier or more intense.' Says Zangrilli, 'Some olfactive families are easier to mix than others: woods and spices don't always play well with air, water, or sport. But both can work with florals and citruses.'
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Some suggested 'winning combinations' for beginning to layer include the following:
Spicy + sweet
Fresh + rich
Fruity + floral
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Experts suggest following one's intuition for guidance in picking out scents to mix, but also using self-knowledge and some common sense. 'There is no right or wrong,' Rahmé says. 'Creating a perfume is part science, but it really is an art - the art of translating emotion into a feeling.' When asked if certain scents should be avoided in layering, she says that an individual should feel free to choose as many layers and types as they feel are necessary to express their vision, but that it is a good idea to avoid combining two or more scents with very strong personalities, such as those that are dark and heady, since their sum can be overwhelming. Perfumer Sue Phillips likens fragrance mixing to choosing spices when cooking: 'Individually, each spice is amazing, but if you were to combine every single one in your cabinet, you'd end up with a blend that was overpowering and indistinct.'
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Most experts agree that limiting the layering to 3-6 accords or scents is a good idea in order to avoid sensory muddling and chaos, or too much smell altogether. Another recommendation is to first try layering older, more stable scents (especially florals and orientals), rather than using the newer chemical synthetics that have fragile balances and that tend to cancel each other out more easily. Griffin-Black says that the easiest way to avoid this pitfall is to choose natural scents. 'If that's not possible,' she continues, 'Be careful about how you layer the synthetic fragrances... Be aware of scents that mask the others and those that blend in an odd way. For natural scents, it's best to start with the strongest you will be layering: scents that include ylang-ylang, jasmine, or patchouli, for instance. Then add the softer scents bit by bit until the right balance is reached.'

Once you find a combination you like, you can fine tune the formula. Says Benaim, 'Something as simple as changing the amount of each fragrance you're mixing can make the blend even more distinct.' Start with one spray of each, the try a 2-to-1 mix, then reverse the ratio or try a 3-to-2 mixture. Once you find exactly what you're seeking, be sure to write it down so that you can recreate it accurately in the future. (Also write down the time of day, the season, and the weather, since these influence the effects.)
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Griffin-Black's advice is to familiarize yourself with scents and figure out first which ones you especially like. Once you are familiar with the notes of given fragrances, it is easier to determine ways to mix and match them for layering. 'The main tip I would share is to wear what you like. Scent is subjective, what you like isn't going to be right for everyone. Choose scents that make you feel good. Take the time to get used to the scent before mixing it with others; what we smell when we first take a breath of a perfume is very different that what it will smell like as it dries down. Use your new scent on both your skin and on clothing, since some smell better on one or the other. If you prefer the scent on fabric more than on your skin, you can apply a drop or two on the inside seams of collars and cuffs.'
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Rahmé recommends keeping the pyramid scent structure in mind when starting to combine, considering an increasing scale of volatility, from musks, then animalics, resins, dark woods, blond woods, hot spices, rich flowers, soft flowers, fruits, leaves, fresh spices, and finally citruses. Too much focus on more volatile notes will produce great projection but little duration, while too much density will come off as flat. In other words, one can 'distribute' the weights of notes to build a pyramid and achieve harmony. An approach that most experts recommend is to start with a heavier base scent or two, then add middle heart notes, and finally finish with lighter top notes. As a foundation of the mixture, the base note(s) provide a grounding, warm richness. Using only one base note spritz helps to create a lighter overall fragrance, while two sprays (for a 2-to-1 ratio to the heart or top notes) creates more depth.
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In this way, one can also tailor a mixture to the season and weather. Says Firmenich perfumer Honorine Blanc, 'In the fall and winter, we might want something cozy and slightly richer and warmer, like the feeling of a comfy sweater that we want close to our skin in cold weather. Putting on a complementary lotion for our scent can add intensity and long-lastingness to our wearing experience. In the spring and summer months, though, you might have a desire for something cleaner and fresher, like combining citrus and floral notes with musky cotton notes.' Others suggest adding the sweeter citrus notes in the colder seasons in order to provide some spiritual lift to heavier mixtures. (Or for those feeling most adventurous, different accords or products can be juggled to create more 'masculine' or 'feminine' character to a combination.) A further step in layering is to add different scents during the course of a day, connecting the user to each present moment as circumstances and mood change. Or a layered scent mixture can be freshened up at midday with a spritz of the top note(s). In answer to the question of which occasions are best for layering, Lee answers, 'There is no limit.' Fragrance combining can be used day to day to suit your mood, style, or the season, and for that special occasion.'

All layering experts agree that persistence is important: if one combination of scents does not seem to work well, juggle the ratios or try a different mix, and play with the different tactics for application. They point out that a large part of the enjoyment of layering comes from exploration and discovery. Says Benaim, 'This is all about experimentation. There are infinite combinations that you can create, and the only way to know if one is going to work is to try it.' (A tip from the perfumers: If you feel like sniffing the mixtures is dulling or burning out your sense of smell, take a break and smell a plain tissue paper; its neutral scent can help to cleanse your 'nasal palette.')
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Layering of scents does not necessarily mean spraying two perfumes directly on top of each other. Instead, it can start as a first application of a body lotion after a shower, followed sometime later by a fragrance preparation behind the ears and on the wrists.
In the Middle East, it was a ritual for women to first apply a musk-based cream to the skin, then to scent their clothing and skin with a fragrance mixture. The fragrance blend was personalized each time, frequently with oud, resins, leather notes, saffron, and rose. This approach also was used for centuries in Japan and Korea, where classical layering consisted of putting body milk, cream, or gel on pulse points, then adding talcum powder or deodorant, and finally adding eau de toilette or perfume. Perfume houses that make lines lending themselves especially well to such mixed-product layering include Maison Francis Kurkdjian and Chanel. Some offer items with this specifically in mind, such as the hand creams from Frédéric Malle, Serge Lutens, and Heliotrope.

A layered fragrance can be applied on the wrists and another on the neck, or they can be placed adjacent to each other or overlapping in order to provide a sort of 'semi-mixing' effect. Perfumers who promote layering sometimes suggest putting the weakest or favorite scents closer to the head area and on pulse points so that they are smelled best, while putting stronger or less favored aromas on the knees or on the clothes. Some experts suggest using two different concentrations of a given scent, such as spraying an eau de parfum on two or three places first, followed by a spray of an eau de toilette; or starting with an oil-based fragrance and then following with a more volatile alcohol-based one. As with the creation of a fragrance mixture, the general rule of thumb is that heavier or complex scents should be put on first so that they don't overpower the simpler, lighter counterparts. Experts also agree that prepping the skin first by using a hydrating body lotion (unscented or very delicately scented) will add to the overall effectiveness of layering.

Some perfume brands seem to lend themselves especially well to layering, including Vilhelm, Atelier Cologne, and Francis Kurkdjian. Jo Malone London, a pioneer in commercial fragrance layering, has incorporated layering into its marketing strategy, producing relatively homogeneous scents so that one knows clearly what is being mixed when layering. They also offer professional consultations for customers, in which the client can experiment with a large variety of combinations. The cosmeticians of Jean Coutu offer the same service.
 
Frankincense

Frankincense, also known as olibanum (or Levonah, Luban, Khunk), is an aromatic, congealed, resinous sap obtained from trees of the genus Boswellia in the family Burseraceae. The name comes from the Old French encens ('high-quality incense'); the word franc meant 'noble' or 'pure.' Its other name, olibanum, comes from the Arabic al-luban ('that which results from milking'), possibly a reference to the milky resin.
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True frankincense comes from five main species, the purest from Boswellia sacra. The gum resin is produced under the bark of small tree shrubs that grow in limestone-rich rocky outcrops, cliffs, or dried riverbeds of Southern Arabia (the Dhofar region of Oman and Yemen), India, and Northern Africa (Somalia, Ethiopia, Eritrea, and Kenya). It sometimes sprouts even on solid rock by means of attachment by a bulbous disk-like swelling of the trunk. (This feature is slight or absent in trees that grow in less stormy areas or in rocky soil or gravel.) The plants obtain moisture from morning mist. Trees begin to produce resin at about 8-10 years of age. The resin is harvested by striping (making incisions in the bark) and then allowing the exuded resin to bleed out and dry for about a week into streaks called tears before being cut off as hardened crystal and then hand-sorted for quality. The longer it is left on the tree, the harder it becomes. Striping or tapping is usually done twice a year (spring and fall), with the final tap generally producing the best resin due to its higher content of aromatic terpene, sesquiterpene, and diterpene. Differences in soil and climate create even more diversity of the resin. It is graded by quality based on aroma, purity, color, age, and shape, with the first, lowest grade being the most common. This grade is brownish and has many bark particles in it. The highest grades are called Silver and Jojari. Most of the annual harvest comes from Somalia and India, and the finest resin is said to come from Somalia and Djibouti, where the Roman Catholic Church purchases most of its stock for incense.
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The dried resin is crushed to a powder, put into an oil bath, and steam distilled to produce the essential oil. Content of essential oil in the resin is about 8%. The distilled liquid is pale yellow-brown to green and has a very strong aroma.
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Frankincense tree populations appear to be declining gradually, partly due to over-exploitation by populations with few other sources of income, which decreases germination rates. In addition, burning, grazing, insect attacks, destruction in armed conflict, and conversion of frankincense woodlands to food agriculture in poverty-stricken areas are decreasing the numbers of trees. In 1998, the International Union for Conservation of Nature warned that Boswellia sacra was 'near threatened,' and a 2006 ecological study demonstrated that Boswellia trees were becoming more difficult to find. A 2019 study predicted a 50% reduction in some Boswellia species within two decades.

Popular folk etymology suggests a connection with the Franks (especially Frankish Crusaders), who reintroduced the spice to Western Europe during the Middle Ages. Frankincense has been traded on the Arabian Peninsula and used in religious ceremonies for thousands of years (and named in Christianity as one of the three gifts from the Magi to the infant Jesus). Some of it was traded as far as China. The Greek historian Herodotus noted that frankincense resin was dangerous to harvest because of venomous snakes that lived in the trees, and he described an Arabian method of burning the gum of the styrax (snowbell) tree to produce smoke that drove the snakes away.

In perfumery, the odor profile is sweet, balsamic, somewhat green, warm, woody, and spicy with a hint of citrus and a piney undertone. Initially it is reminiscent of freshly ground black pepper with a lemon peel twist, and as it dries down it reveals its woody character, both rich and crisp, with a dark, balsamic finish. With both cold and warm elements, it is quite versatile. It is associated often with Oriental and heavy, dark fragrances, especially those with amber, cedarwood, spices, vanilla, and patchouli. But it also supports and blends quite well with lighter, effervescent orange, bergamot, and green tones.

Frankincense has been used in perfume products, essential oils, cleaning products, cosmetics, pharmaceuticals, and 'natural' medicines. It is inhaled in aromatherapy or applied to the skin for its supposed health benefits, including calming, clearing, and relaxing the mind. Folk remedies include it for treatment of nausea, indigestion, cough, hypertension, depression, and anxiety. In Chinese medicine, frankincense (called ru xiang), when combined with myrrh, was thought to have antibacterial properties as well as blood-stimulant value, when used topically or orally. In Persia, it was said to be used for diabetes, gastritis, and stomach ulcers, and ancient Egyptians cleansed body cavities with frankincense and natron during the mummification process. By itself or in incense (its most common use), it has been burned in many Hebrew and Christian churches, including Eastern Orthodox, Oriental Orthodox, and Roman Catholic, partly because it is believed to aid prayer and meditation. Both Christian and Islamic faiths have mixed it with oils to anoint newborn infants and church initiates and in burial rituals. The resin powder or oil are put into potpourri, and oil and smoke from burning incense are used commonly to scent room air. In addition, the smoke is effective for driving away mosquitos, thus reducing the incidence of malaria. Finally, frankincense can be used as a flavoring agent, giving a peppery-balsamic flavor. It is added to foods, drinks, and toothpastes, and in the parts of the Middle East it is chewed as a gum to freshen the breath.

Masculine fragrances with significant frankincense:

Abercrombie & Fitch Oud Essence
Amouage Jubilation for Men
Armand Ultimate Drive
Aquaflor Firenze Azar
Armani Privé Bois D’Encens
Ashley Oud pour Lui
Aziza Dark Entity
Bvlgari Aqva Amara; Kobraa; Ambero
Caron Parfum Sacré
Comme des Garçons Incense Series Avignon
Dior Sauvage
Guerlain Arsene Lupin Dandy
Hermès Eau de Gentiane Blanche
Lise London Perfect Gentleman
Malone London Incense & Cedrat
Mauboussin Cristsal Oud
Osmo Encens Epice
Prada Infusion d'Homme
Regence Kolnisch Juchten
Sonoma Incense Pure
Tauer Incense Extreme
Zegna Passion
 
Aromatic Extraction Techniques in Perfumery

Before perfumed products can be composed, the odorants used in the various perfume compositions must first be obtained. Synthetic odorants are produced through organic synthesis. The term "aroma extraction" refers to the extraction of aromatic compounds from raw natural plant materials, using methods such as distillation, solvent extraction, expression, or enfleurage. The results of the extraction are essential oils, absolutes, concretes, or butters, depending on the amount of waxes in the extracted product. The different methods have been devised to make the extracted material smell as much like the donor plant as possible and to be cost-effective. To a certain extent all of these procedures are damaging: they denature the aromatic compounds, changing their odor profile or even making them totally odorless. This has to do with the materials themselves having so little volatile oil that they do not yield a sufficient crop (lily of the valley and gardenia, for example) or being too delicate to withstand techniques that employ heat, harsh solvents, or exposure to oxygen.

Commercial Extraction Processes

EXPRESSION

Expression is among the oldest methods of fragrance extraction. Aromatic essential oil is produced from plants that are squeezed or compressed, forcing the complete oil out. These oils were first produced in Egypt in unglazed ceramic vases, with the flowers pressed and then buried in the desert for driving out the moisture. The water has a smaller molecular size, so it diffuses through the ceramic vessels, while the larger essential oils do not. The lotus oil in Tutankhamen's tomb, which retained its scent after 3000 years sealed in alabaster vessels, was pressed in this manner. Expression is an especially mild process, historically used in cases where steam distillation would modify or damage the end product. Today the only oils obtained by expression are those from the rinds of citrus fruits, due both to the abundance of aromatics in this squeezable part of the fruit and to the low cost of growing citrus fruits in general. This method is sometimes called cold pressure extraction.


DISTILLATION

Distillation, using an alembic (an alchemical still consisting of two vessels connected by a tube), is an advanced method developed in the Middle Ages and is now a common one, used for rendering a variety of aromatic essences, with the raw material sources being wood, bark, roots, flowers, leaves, seeds, peels, and flowers. In this procedure, a carrier solvent (usually water but sometimes another liquid such as alcohol) is boiled and its steam is passed through the raw material in the still for 60-100 minutes, taking the fragrant substances along with it. After cooling and condensing of the vapor, the essential oil, which floats to the top, is separated from the distillation water in Florentine flasks. The resulting material is still mostly called an essential oil, comprising aromatic and volatile ingredients of the raw material. Several very common essential oils such as peppermint, basil, lavender, rose, palmarosa, geranium, sandalwood, and eucalyptus, are produced in this way. Distillation produces different quality grades of essential oils, making some finer than others. The water collected from the condensate, which retains some of the fragrant compounds from the raw material after the oil is removed, is called hydrosol and is also sometimes sold. Examples are rose hydrosols and orange blossom hydrosols.

Rectification (also called dry or destructive distillation): The raw materials are directly heated in a still, without a carrier solvent such as water or alcohol, and often in the absence of air. Fragrant compounds that are released from the raw material by the high heat undergo anhydrous pyrolysis, which results in the formation of different compounds and thus different fragrance notes that can be used in perfume compositions. This method is used to obtain fragrant compounds from fossil amber and fragrant woods, where an intentional "burned" or "toasted" phenolic (tar-like) odor is desired. Examples are birch tar oil and Styrax pyrogenated oil.

Fractional distillation: A prolonged process is used, employing a fractionating column, which renders several grades of the aromatic compound, varying in quality and depth of scent. This allows for greater control of the qualities of the end material produced and is therefore very helpful in allowing manipulation of the effects they have in a fragrance formula. Although the product of fractional distillation is more expensive, this process is sometimes necessary to remove unpleasant or undesirable scents of a material. It is commonly used for ylang-ylang.


SOLVENT EXTRACTION/MACERATION

Organic solvent extraction is the most common and most economically important technique for extracting aromatics in the modern perfume industry. Raw materials are submerged in a solvent that can dissolve the desired aromatic compounds. Commonly used solvents for maceration/solvent extraction include hexane, ethane, and dimethyl ether.

Fragrant compounds from woody and fibrous plant materials are often obtained in this way, as are all aromatics from animal sources (although this is increasingly uncommon due to ethical concerns). The technique can also be used to extract odorants that are too volatile for distillation or are easily denatured by heat. The remaining waxy mass is known as a concrete, which is a mixture of essential oil, waxes, resins, and other lipophilic (oil-soluble) plant material. Although highly fragrant, concretes are too viscous - sometimes even solid - at room temperature to be useful. This is due to the presence of high-molecular-weight, nonfragrant waxes and resins. Another solvent, often ethanol (ethyl alcohol), which only dissolves the fragrant low-molecular-weight compounds, must be used to extract the fragrant oil from the concrete. The alcohol is removed by a second distillation, leaving behind what is called the absolute. Due to the lower temperatures used in this process, the absolute can be more faithful to the original scent of the raw material than are the products of distillation.

To differentiate between an absolute and a tincture: A tincture is a material produced through use of ethanol extraction directly from dry materials submerged in the alcohol, while absolutes are rendered through washing and effectively purifying with ethanol the waxy materials (oils, concretes) derived from solvent extraction/enfleurage.

Supercritical fluid extraction: In supercritical fluid extraction, a relatively new method, high pressure carbon dioxide gas (up to 100 atm) is used as a solvent. When carbon dioxide is put under high pressure at slightly above room temperature, a supercritical fluid forms. (Under normal pressure, CO2 changes directly from a solid to a gas in a process known as sublimation.) CO2 in a non-polar compound has low surface tension and wets easily, and it can be used to extract the typically hydrophobic aromatics from the plant material. This process is identical to one of the techniques for making decaffeinated coffee. Like solvent extraction, CO2 extraction takes place at a low temperature, extracts a wide range of compounds, and leaves the aromatics unaltered by heat, producing an essence that is very faithful to the original. Since CO2 is a gas at normal atmospheric pressure, it also leaves no trace of itself in the final product, thus allowing one to get the absolute directly without having to deal with a concrete. Extracts produced using this process are known as CO2 extracts.


INFUSION

Water maceration produces an infusion, a familiar term from tisanes/herbal teas and a comparable technique. The plant material is submerged in hot water (or alcohol or oil) and left to marinate (steep) for a period of time, yielding its aromatic properties. Then the plant is removed with a strainer and the water remaining is called an infusion. The process of infusion is distinct from decoction, which involves boiling the plant material, or percolation, in which the water passes through the material (as in a coffeemaker). Infusion is a very simple chemical process used with botanicals that are highly volatile and dissolve readily or release their active ingredients easily in the liquid. The botanicals are typically dried herbs, flowers or berries.


DECOCTION

Decoction is a method of extraction by boiling out dissolved chemicals from mashed plant material, which may include stems, roots, bark, and rhizomes. Decoction produces liquids with differing chemical properties than those of infusion because the temperature/preparation difference results in more oil-soluble chemicals in decoction than in infusion. Decoction is also the name for the resulting liquid.


ENFLEURAGE

Enfleurage is a famous but now antiquated process, prized in years past for its capacity to capture the mature, deep aroma of delicate flowers, such as jasmine or tuberose, that lost their precious aromatic bouquet in high-heat distillation. Enfleurage in the original French means to “impregnate with the scent of flowers.” It is also defined as “extracting perfumes by exposing inodorous oils or fats to the exhalations of flowers.”

The technique uses animal fat (deodorized lard or tallow) as a waxy 'dress' for the flowers, allowing them to macerate for days on large glass plates in wooden frames. Fresh produce was added to the point of fragrance saturation. The fragrant fat 'pomade' was then washed with ethanol to render an 'absolute de chassis.' Two variations of the technique existed: 'cold' enfleurage, perfected in the 19th century and using no external heat, and 'hot' enfleurage, in which the fat was gently heated while the botanical matter was stirred into the fat.

This technique is not commonly used any longer in the perfume industry, due both to its prohibitive labor intensity and cost and to the existence of newer, more efficient extraction methods such as solvent extract and supercritical fluid extraction.


Otto, Attar, and Monoi

Otto (most often rose otto, but also including saffron, lotus, and jasmine osttos) is essential oil derived from the petals of flowers. Rose otto is produced from different varieties of roses through steam distillation (as opposed to the absolute, which is produced through solvent extraction or supercritical CO2 extraction). The finest rose otto is produced in Turkey and Bulgaria. Ottos are used less often in perfumery than absolutes.

Attar is the English form of the Arab term ittar, an ancient Persian word meaning "to smell sweet." It is used to denote a variety of natural oils rendered from botanical sources, especially those that do not contain any added alcohol. The oils are most often distilled into a wood base such as sandalwood and then aged. The aging period can last from one to ten years depending on the botanicals used and the results desired. Attars are highly concentrated and therefore are usually offered for sale in small quantities in decorated crystal cut bottles or small jeweled decanters. The terms attar and otto are sometimes use interchangeably.

A variation on this is the famous Monoi ("scented") oil, which uses Tiaré flowers (i.e. Tahitian gardenias), macerated and distilled in coconut oil (which is a semi-solid wax substance in its pure form).
 
"Notes" and the Pyramid Scheme

Often seen in a description of a fragrance is a list of "notes" that it contains, frequently arranged in pyramid form with top, middle, and base notes separated into groups. Sometimes a note refers to an actual discrete ingredient such as rose or orange blossom, but other times it is more loosely used to represent an interaction of two or more factors, and “accord” would be more accurate. This pyramid description provides a useful way to envision a fragrance as it would develop after application. Since fragrant materials differ in their volatility, the olfactory impression of the fragrance changes as it dries down on the skin. So theoretically, first one would smell the most volatile notes, such as citrus and fruit; then the florals would be smelled; and finally one would detect the least volatile musks and woods. However, the fragrance pyramid mostly applies to perfumes created between the 1930s and 1970s. The study of different fragrance materials and their classification in terms of volatility was perfected early in that era by the perfumer Jean Carles (1892-1966,) whose own work on some great classics exemplified the classical pyramid structure. These fragrance mixes were built with a very clear three-dimensional quality, with the characters of the top, middle, and base being very distinct. Earlier 20th century fragrances, prior to the 1930s, were not formulated as a classical pyramid, but were much closer in character to the fragrance blends of the 19th century, based on the use of natural essences fixed in place by oriental components (balsamic, exotic aromas) and animalic materials (such as civet, ambergris, and castoreum, unpleasant in large amounts but providing depth and sensuality in lower concentrations).

A perfume is a unique mixture of scented materials with its own distinctive character that is more than just a sum of its parts, and the list of notes tells only a part of the story. In addition, fragrances made today no longer adhere strictly to the three-tiered structure. Over the past 40 years, there has been a marked shift away from the fragrance pyramid concept and into new structures that give much different impressions. To use a musical metaphor, the theme is there in many modern fragrances from the first movement, and even if you hear a violin at one point and a flute later, the character remains unchanged throughout. Some fragrances might even lack altogether a top note in the classical pyramid sense, with the initial impression being set by a small amount of extremely strong materials that would more typically be considered as middle or base notes. In contrast to more subtle classical mixtures, modern fragrances do not hide or bury their themes, and they frequently represent open character declarations, with side scent notes providing harmonious texture details to the overall "melody." Modern fragrance structures are not necessarily simple, as the creative layering of accords can result in fragrances of remarkable complexity.

Finally, the sheer number of new fragrance launches means that consumers, face with numerous choices, often make decisions based on their first impressions. Fragrance compositions, as well as their descriptions, often are driven by sales considerations, and the pyramid list of notes is sometimes just a marketing concept, crafted for different emphases. For example, some brands might try to avoid listing a perceived heavier component such as musk in their fragrance notes even though their products contain it. Other brands, on the other hand, may want to emphasize and promote notes that they feel are most suited to their concepts: if a fragrance is launched as the new floral to fill a gap in the brand’s product portfolio, its floral notes will be highlighted in the description, even if they play a relatively minor role in the total fragrance composition. Moreover, a descriptor may be inaccurate. A term such as jasmine may not even mean anything that smells truly like a jasmine flower — it may be a luminous hedione note (an ester resembling natural jasmine but actually closer to lily of the valley in character) or a raw material representing just one facet of the flower. And those "woods" anchoring the bottom of a fragrance pyramid scheme are likely to be Cashmeran, a synthesized chemical with a complex woody-musky note.

While the fragrance notes are helpful, they should be seen only as a rough guide. However, since they provide an easily shared and communicated structure, they are commonly used and can be a basis for comparison.

In the pyramid scheme, the olfactory impression of a fragrance is described in a musical metaphor as having three sets of notes, which together constitute the harmonious overall scent accord. Notes are descriptors of individual scents or scent interactions that can be perceived upon the application of a perfume. They are separated into three classes: top/head notes, middle/heart notes, and base/back notes, which denote scents grouped with respect to their varying times for being perceived after application of the fragrance on the skin. Generally, then, this is a volatility grouping, based on a scheme using their respective evaporation coefficients from 1 to 100:

Top Notes: 1 to 14 (most volatile)
Middle Notes: 15 to 60
Base Notes: 61 to 100 (least volatile)

Top or head notes are perceived immediately upon application of a perfume. The compounds that contribute to top notes are strong in scent, are very volatile, and evaporate quickly. They form a person's initial impression of a fragrance and thus are very important in the selling of the product. The scents of this note class are often described with terms such as "fresh," "assertive" or "sharp." Citrus scents and ginger are common top notes.

Heart or middle notes are the second, middle phase of a perfume's fragrance evaporation, occurring after the top note fades away. The heart stage is mainly produced by floral, spicy or woody components, and as its name indicates, it usually represents the heart or dominant tone of the perfume and enables its classification into a fragrance family. Common heart notes are jasmine, rose, lavender, and various herbs. These notes appear anywhere from 2 minutes to an hour after fragrance application, but most commonly require around 10 to 20 minutes to develop fully on the skin. The scent of middle note compounds is usually perceived as mellow and "rounded." These notes often mask initially the unpleasant impression of the later base notes, which become more pleasant over time.

The back or base notes (or fond, meaning "bottom" in French) are the third and last phase of a perfume's life on the skin, the underlying tones that bring solidity and depth. This phase contains the lasting ingredients, such as woods, resins, and animal and crystalline substances. These are the heaviest ingredients, molecularly, in a perfume formula. In heavy fragrances (chypre and Oriental types, for instance), the back note group is so strongly accented that it is even discernible as a first impression along with the top or head notes. Base notes sometimes impart their own scent; they help to fix other notes in the perfume formula (i.e. make them last longer); and they enhance or boost other, lighter ingredients. Base notes generally appear most prominently close to the departure of the middle notes, and the base and middle notes together frequently define the main theme of a perfume and its lasting impression on the person smelling it. Consisting of large, heavy molecules that evaporate slowly, compounds of this class of scents are typically rich and "deep" and are usually not perceived until at least 30 minutes after the application of the perfume or during the period of perfume dry-down.

As noted in terms of the effect of base notes, it should be kept in mind that the presence of one note may alter the perception of another - for instance, the presence of certain base or heart notes will alter the scent perceived when the top notes are strongest, and likewise the detected scent of base notes in the dry-down will often be altered depending on the fragrance materials and lingering smells of the heart notes.
 
Grapefruit

The grapefruit (Citrus paradisi or Citrus x paradisi) is a small subtropical citrus tree known for its relatively large fruit. Although its botanical origins are uncertain, it appears to have come originally from northern China. It is thought to be a natural hybrid originating in Barbados as an accidental cross between the Jamaican sweet orange (C. sinensis) and the Indonesian pomelo or shaddock (C. maxima), both of which had been introduced to the West Indies from Asia by English captain Philip Shaddock by around 1692. The evergreen grapefruit trees usually grow to around 5-6m (16-29 ft) tall but can reach 30m, with a single trunk and many branches. The leaves are glossy, dark green, long, and thin. a tree produces white four-petaled flowers. The fruit's outer skin is light yellow- to orange-skinned (although a few are green) and generally is spherical, ranging in diameter from 10 to 15cm (4-6 in).
IgAgAKC.jpg
M3QwAF4.jpg
mVG53w6.jpg


The tree was first cultivated documented in 1750 by a Rev. Griffith Hughes, who described it in his 'The Natural History of Barbados' and called it the 'forbidden fruit' because it reminded him of the biblical apple in the Garden of Eden. In 1814, naturalist John Lunan first used the term grapefruit in print to describe a similar Jamaican citrus plant, reporting that the name was due to its similarity in taste to the grape (Vitis vinifera). However, an alternative explanation was offered by botanist François Richard de Tussac, who suggested that the name may refer to clusters of fruit on the tree, appearing similar to grape bunches.
Yi0YdT5.jpg
uqwoAa1.jpg
CcGgjzt.jpg


From Barbados, the plant was introduced to Florida in 1823 by Count Odet Philippe (the first permanent, non-native settler there), where it quickly became popular. Subsequent crosses produced the tangelo in 1905, the Minneola tangelo in 1931, and the oroblanco in 1984. Kimball Atwood founded the Atwood Grapefruit Company in the late 19th century, and its planting became the largest grapefruit grove in the world at the time, with a yearly output of 80,000 boxes of fruit. The pink grapefruit was first discovered there in 1906.
y0kfcdJ.jpg
NUqo6ET.jpg
BBUofRQ.jpg


The fruit's interior flesh is segmented, and its colors range from white, through pale yellow or blush-pink, to ruby red. The darker coloration is due to the presence of lycopene. They are rich in nutrients, fiber, vitamins, and minerals. The taste is sour to semi-sweet or bitter. With ongoing research, horticulturalists learned how to remove the bitterness and improve the fruit's sweetness while still maintaining the tangy flavor. Grapefruit flavors result from varying compositions of sugars (mainly sucrose) and organic acids (mainly citric acid). The sweetest and least acidic are the red varieties, but yellow and pink ones are the most common. Radiation has been used to develop plants whose fruit retained the red tones that would usually fade naturally to pink.
NlKlidW.jpg
Brgv7I5.jpg


The major commercial varieties are the Pink, Ruby Red, Star Ruby, Thompson, and White March, with the color name usually referring to the fruit's flesh and not the peel. The Star Ruby is the darkest of the red varieties; it has found only limited commercial success because it is more difficult to grow. The most popular grapefruit is the Ruby Red (or Reblush), patented in 1929 after it was discovered growing on a pink variety as a limb sport (a part of a plant that shows morphological differences from the rest of the plant).
Q6f2RYq.jpg


The US was for a long time the leading grower of grapefruit, but it has been overtaken by China. World production of grapefruit in 2019 was 9.3 million tons, of which 53% came from China. Other significant producers include Vietnam (0.8 ton), the United States (0.5 ton, mainly Florida), Mexico (0.5 ton), and South Africa (0.4 ton).
IbQVV4K.jpg


Commercial grapefruit oil is produced mainly in the US, the West Indies, Brazil, Israel, and Nigeria. The oil is expressed (cold pressed) or distilled from the peels, and to a lesser extent the seeds or even the whole fruit. The essential oil separates naturally from the pressed juice. Most commercial oil comes from the Duncan variety, light yellow fruits with a very light-colored flesh. It is thin and watery and yellow to green-yellow or pale orange-yellow in color. Since oil glands are located more deeply in grapefruit peel than in other citrus fruits, its oil is more difficult to extract and is more expensive than oils of lemon and orange.
q2v6ReQ.jpg
HRqxar7.jpg


A study in 1980 demonstrated that Florida grapefruit oil has at least 32 volatile compounds, and a 2001 study showed that 22 of them had significant aroma activity. In another study in 2002, limonene (93%), myrcene (1.5%), sabinene (0.6%), and α-pinene (0.6%) were determined as major aromatic compounds. Tisserand and Young (2014) reported similar results on grapefruit essential oil composition, confirming that it consisted mainly of limonene (90%) and bergamot (27%–52%). The aroma of grapefruit oil seems to be due mainly to the terpenes. The primary one is mercaptan (thiolimonene), which along with nootkatone are the substances that give a sulfurous 'tropical' character which differentiates grapefruit's smell from those of other citrus fruits. Mercaptan is extremely intense, providing its fruity note even at a presence of less than one part per billion in the oil. A major scent contribution also comes from natural saturated aldehydes, especially octanal, decanal, and dodecanal.
JZZcauB.jpg


There is substantial chemical variation existing in the peel oil from different cultivars grown in the same region, as well as from cultivars grown in different regions, resulting in a wide range of grapefruit aroma qualities and standards. In addition, cold-pressed grapefruit oil sometimes is adulterated by the addition of lower-quality steam-distilled oil, isolated grapefruit terpenes, and sweet orange terpenes. Like most other citrus oils, grapefruit oil is unstable and deteriorates easily upon exposure to moisture, air, and daylight.

In order to create a brighter and more convincing citrus-smelling perfume ingredient, producers reduce the amount of limonene in the oil, usually by distilling it off under pressure at low temperatures. These are called 'folded' oils. For example, the designation '5x fold' or '5-fold' means that the oil must be diluted 5 times with limonene to return it to its original unfractionated version.
gCYnNk8.jpg


In his book 'The Diary of a Nose,' perfumer Jean-Claude Ellena expresses regret that natural grapefruit essential oil smells too much like orange, lacking somewhat the overall character of the smell of the fresh fruit. The smell that differentiate grapefruit somewhat from the other citruses is a particularly bitter, herbaceous woody aspect that is reminiscent of vetiver. This is mainly determined by nootkatone, whose concentration in the oil varies from 0.5% to 2%. The color of the fruit correlates directly with its overall scent composition: white grapefruit, sharp and bitter, has the highest amount of nootkatone and other minor components; while more intensely colored varieties, sweeter and more sensual, contain less of these substances but have a higher aldehyde content.

The chemical synthesis of nootkatone, now being used to fulfill market demand for grapefruit aroma because of low yields from natural plant sources, uses harmful chemicals and is very expensive. It takes about 4 tons of grapefruit to make 1kg of nootkatone. Therefore, attempts are being made to produce nootkatone from microbes through biotechnological approaches. The company Biotrans produces nootkatone from natural valencene derived from oranges, using the enzyme cytochrome p450. This can be called natural in product labeling but cannot be called 'natural grapefruit.'
cpri2Iq.jpg


Synthetics, primarily vetivone and valencene, are also used now in modern perfume products. Their odors provide a number of different facets in varying combinations. Each has its own nuances: dimethylcathinone and fructalate smell very fresh and citrusy; floropal and rhubafuran have rhubarb, green scent, with a touch of marijuana; khusinil, vigoflor and rhubofix share a distinct woody character, reminiscent of vetiver. Rhubofix in particular mimics the qualities of nootkatone. The synthetics, lasting longer than the natural scent components, are sometimes used as middle or base notes.

Citrus essential oils are the most popular group of aromatics in the natural fragrances market, although they are not universally admired, and grapefruit is not among the most favored citruses. In the 1990s, it was mainly used in the top citrus notes of masculine fragrances, but it is employed more widely now. It is a main ingredient of woody aromatic blends, especially summer compositions. Members of the chypre family frequently contain grapefruit along with other citruses, often paired with vetiver, oakmoss, iris, amber, and patchouli.

Grapefruit aroma offers an energetic yet calming and elegant aspect that sets it apart from other citrus fruits. It is lively and sparkling, fresh, cooling, and somewhat sour to bittersweet. As a result of continued cross-breeding, the essential oil's fragrance, like the taste of the fruit, has become 'softer' and with less character than in the past. The grapefruit scent note blends especially well with bergamot, mandarin, neroli, basil, frankincense, peppermint, rosemary, chamomile, clove, black pepper, nutmeg, fennel, ginger, lavender, oakmoss, cypress, cedarwood, rosewood, balsam, juniper, geranium, jasmine, patchouli, and ylang-ylang. The oil breaks down on the skin to form somewhat malodorous compounds, so fruit ester 'modifiers' are sometimes added to it to maintain a fresher floral scent after application.

Grapefruit has a long history of use in folk medicines around the world and has been used traditionally as an antibacterial, antifungal, anti-inflammatory, antioxidant, astringent, and preservative. It is has popular as a remedy for cellulite and as an antidepressant. In aromatherapy, it is thought to be calming but stimulating and uplifting. It is also used commercially as a flavoring agent in foods and beverages and as a fragrance ingredient in soaps, detergents, and personal care products.

Masculine grapefruit fragrances:

Acqua di Gio Essenza
Agonist Solaris
Alfred Dunhill X-Centric
Alendor Taboo
Antonio Puig Quorum
Aramis Havana
Atelier Cologne Pomelo Paradis
Athena Vetiver
Autre Parfum Avant-Garde
Azzaro Chrome (various), Azzaro Jetlag, Azzaro LE 2016
Baldessarini Del Mar Marbella
Barbour
Benetton White Night
Bvlgari Aqua Marine, Bvlgari Man Extreme, Bvlgari Tygar
Burberry Mr. Burberry, Burberry Sport, Burberry Weekend
By Killian Smoke for the Soul
Carolina Herrera 212 Summer 2013, CH 212 Surf, CH Sport
Cacharel Amor Sunshine
Cartier Declaration l'Eau
Chanel Bleu
Chopard Malaki
Christian Dior Aqua Fahrenheit, CD Higher Energy, CD Homme Sport, CD Vetiver
Creed Himalaya
Davidoff Good Life
Dolce & Gabbana Light Blue, D&G The One
Dzintars Sudrabotais Ledus Blue
Emanuel Ungaro Fresh
Estee Lauder Pleasures
Fiorucci Extreme Sport
Giorgio Armani Night
Giorgio Beverly Hills Ocean Dream
Givenchy Blue Label, Givenchy Fresh Attitude
Guerlain Aqua Allegoria Pamplelune, Guerlain l'Instant
Guy Laroche Drakkar Dynamik
Hermes Terre d'Hermes
Hugo Boss Boss in Motion, HB Boss Pure, HB Boss Selection, HB Boss Unlimited, HB Hugo Dark Blue
I-Scents Premium Blue Concept
Issey Miyake Sport Polar Expedition
Jacques Bogart Riviera Nights
Jean Paul Gaultier Le Male Terrible
Jeanne Arthes Joe Sorrento Sport
Jequiti Abyssal Homem Energy
Jo Malone Grapefruit
Kenzo Fresh
Korres Neos
Lange Orient Treasure
Loewe Sport Edicion Especial
Louis Cardin La Viola
Mont Blanc Emblem
Moschino Forever Sailing
Oriflame Ascendant Aqua, Oriflame Eclat Lui
Paco Rabanne 1 Million, PR Invictus
Paul Sebastian Silver
Paul Smith Sunshine Edition
Sean John Unforgivable Night
Tom Ford Mandarino di Amalfi
Tommy Hilfiger Freedom, TH True Star
Victorio & Lucchino No7 Frescor Mediterraneo
Viktor & Rolf Spicebomb
Yves Rocher Cypres et Pamplemousse
Zara Denim Couture, Zara Navy Black, Zara Norrland, Zara Vibrant Leather Parfum de Liberte

Pink grapefruit fragrances for men (generally sweeter):

Bvlgari Man Extreme (various)
Carolina Herrera 212 NYC Seductive
Cartier Declaration l'Eau
Emanuel Ungaro Cologne Extreme
Il Profvmo Cafe Vert
Karl Lagerfeld Bois de Vetiver
Kenzo Electric Wave
Kanon Kool
Lacoste Essential Sport
Nautica Gold Rush
Ralph Lauren Big Pony 4, RL Polo Red (various)
S.T. Dupont Paris by Night
Tommy Hilfiger Eau de Prep, TH Hilfiger
Van Gils Strictly for Night
Yohji Yamamoto His Love Story
Zara Black Edition
 
Grapefruit

The grapefruit (Citrus paradisi or Citrus x paradisi) is a small subtropical citrus tree known for its relatively large fruit. Although its botanical origins are uncertain, it appears to have come originally from northern China. It is thought to be a natural hybrid originating in Barbados as an accidental cross between the Jamaican sweet orange (C. sinensis) and the Indonesian pomelo or shaddock (C. maxima), both of which had been introduced to the West Indies from Asia by English captain Philip Shaddock by around 1692. The evergreen grapefruit trees usually grow to around 5-6m (16-29 ft) tall but can reach 30m, with a single trunk and many branches. The leaves are glossy, dark green, long, and thin. a tree produces white four-petaled flowers. The fruit's outer skin is light yellow- to orange-skinned (although a few are green) and generally is spherical, ranging in diameter from 10 to 15cm (4-6 in).
IgAgAKC.jpg
M3QwAF4.jpg
mVG53w6.jpg


The tree was first cultivated documented in 1750 by a Rev. Griffith Hughes, who described it in his 'The Natural History of Barbados' and called it the 'forbidden fruit' because it reminded him of the biblical apple in the Garden of Eden. In 1814, naturalist John Lunan first used the term grapefruit in print to describe a similar Jamaican citrus plant, reporting that the name was due to its similarity in taste to the grape (Vitis vinifera). However, an alternative explanation was offered by botanist François Richard de Tussac, who suggested that the name may refer to clusters of fruit on the tree, appearing similar to grape bunches.
Yi0YdT5.jpg
uqwoAa1.jpg
CcGgjzt.jpg


From Barbados, the plant was introduced to Florida in 1823 by Count Odet Philippe (the first permanent, non-native settler there), where it quickly became popular. Subsequent crosses produced the tangelo in 1905, the Minneola tangelo in 1931, and the oroblanco in 1984. Kimball Atwood founded the Atwood Grapefruit Company in the late 19th century, and its planting became the largest grapefruit grove in the world at the time, with a yearly output of 80,000 boxes of fruit. The pink grapefruit was first discovered there in 1906.
y0kfcdJ.jpg
NUqo6ET.jpg
BBUofRQ.jpg


The fruit's interior flesh is segmented, and its colors range from white, through pale yellow or blush-pink, to ruby red. The darker coloration is due to the presence of lycopene. They are rich in nutrients, fiber, vitamins, and minerals. The taste is sour to semi-sweet or bitter. With ongoing research, horticulturalists learned how to remove the bitterness and improve the fruit's sweetness while still maintaining the tangy flavor. Grapefruit flavors result from varying compositions of sugars (mainly sucrose) and organic acids (mainly citric acid). The sweetest and least acidic are the red varieties, but yellow and pink ones are the most common. Radiation has been used to develop plants whose fruit retained the red tones that would usually fade naturally to pink.
NlKlidW.jpg
Brgv7I5.jpg


The major commercial varieties are the Pink, Ruby Red, Star Ruby, Thompson, and White March, with the color name usually referring to the fruit's flesh and not the peel. The Star Ruby is the darkest of the red varieties; it has found only limited commercial success because it is more difficult to grow. The most popular grapefruit is the Ruby Red (or Reblush), patented in 1929 after it was discovered growing on a pink variety as a limb sport (a part of a plant that shows morphological differences from the rest of the plant).
Q6f2RYq.jpg


The US was for a long time the leading grower of grapefruit, but it has been overtaken by China. World production of grapefruit in 2019 was 9.3 million tons, of which 53% came from China. Other significant producers include Vietnam (0.8 ton), the United States (0.5 ton, mainly Florida), Mexico (0.5 ton), and South Africa (0.4 ton).
IbQVV4K.jpg


Commercial grapefruit oil is produced mainly in the US, the West Indies, Brazil, Israel, and Nigeria. The oil is expressed (cold pressed) or distilled from the peels, and to a lesser extent the seeds or even the whole fruit. The essential oil separates naturally from the pressed juice. Most commercial oil comes from the Duncan variety, light yellow fruits with a very light-colored flesh. It is thin and watery and yellow to green-yellow or pale orange-yellow in color. Since oil glands are located more deeply in grapefruit peel than in other citrus fruits, its oil is more difficult to extract and is more expensive than oils of lemon and orange.
q2v6ReQ.jpg
HRqxar7.jpg


A study in 1980 demonstrated that Florida grapefruit oil has at least 32 volatile compounds, and a 2001 study showed that 22 of them had significant aroma activity. In another study in 2002, limonene (93%), myrcene (1.5%), sabinene (0.6%), and α-pinene (0.6%) were determined as major aromatic compounds. Tisserand and Young (2014) reported similar results on grapefruit essential oil composition, confirming that it consisted mainly of limonene (90%) and bergamot (27%–52%). The aroma of grapefruit oil seems to be due mainly to the terpenes. The primary one is mercaptan (thiolimonene), which along with nootkatone are the substances that give a sulfurous 'tropical' character which differentiates grapefruit's smell from those of other citrus fruits. Mercaptan is extremely intense, providing its fruity note even at a presence of less than one part per billion in the oil. A major scent contribution also comes from natural saturated aldehydes, especially octanal, decanal, and dodecanal.
JZZcauB.jpg


There is substantial chemical variation existing in the peel oil from different cultivars grown in the same region, as well as from cultivars grown in different regions, resulting in a wide range of grapefruit aroma qualities and standards. In addition, cold-pressed grapefruit oil sometimes is adulterated by the addition of lower-quality steam-distilled oil, isolated grapefruit terpenes, and sweet orange terpenes. Like most other citrus oils, grapefruit oil is unstable and deteriorates easily upon exposure to moisture, air, and daylight.

In order to create a brighter and more convincing citrus-smelling perfume ingredient, producers reduce the amount of limonene in the oil, usually by distilling it off under pressure at low temperatures. These are called 'folded' oils. For example, the designation '5x fold' or '5-fold' means that the oil must be diluted 5 times with limonene to return it to its original unfractionated version.
gCYnNk8.jpg


In his book 'The Diary of a Nose,' perfumer Jean-Claude Ellena expresses regret that natural grapefruit essential oil smells too much like orange, lacking somewhat the overall character of the smell of the fresh fruit. The smell that differentiate grapefruit somewhat from the other citruses is a particularly bitter, herbaceous woody aspect that is reminiscent of vetiver. This is mainly determined by nootkatone, whose concentration in the oil varies from 0.5% to 2%. The color of the fruit correlates directly with its overall scent composition: white grapefruit, sharp and bitter, has the highest amount of nootkatone and other minor components; while more intensely colored varieties, sweeter and more sensual, contain less of these substances but have a higher aldehyde content.

The chemical synthesis of nootkatone, now being used to fulfill market demand for grapefruit aroma because of low yields from natural plant sources, uses harmful chemicals and is very expensive. It takes about 4 tons of grapefruit to make 1kg of nootkatone. Therefore, attempts are being made to produce nootkatone from microbes through biotechnological approaches. The company Biotrans produces nootkatone from natural valencene derived from oranges, using the enzyme cytochrome p450. This can be called natural in product labeling but cannot be called 'natural grapefruit.'
cpri2Iq.jpg


Synthetics, primarily vetivone and valencene, are also used now in modern perfume products. Their odors provide a number of different facets in varying combinations. Each has its own nuances: dimethylcathinone and fructalate smell very fresh and citrusy; floropal and rhubafuran have rhubarb, green scent, with a touch of marijuana; khusinil, vigoflor and rhubofix share a distinct woody character, reminiscent of vetiver. Rhubofix in particular mimics the qualities of nootkatone. The synthetics, lasting longer than the natural scent components, are sometimes used as middle or base notes.

Citrus essential oils are the most popular group of aromatics in the natural fragrances market, although they are not universally admired, and grapefruit is not among the most favored citruses. In the 1990s, it was mainly used in the top citrus notes of masculine fragrances, but it is employed more widely now. It is a main ingredient of woody aromatic blends, especially summer compositions. Members of the chypre family frequently contain grapefruit along with other citruses, often paired with vetiver, oakmoss, iris, amber, and patchouli.

Grapefruit aroma offers an energetic yet calming and elegant aspect that sets it apart from other citrus fruits. It is lively and sparkling, fresh, cooling, and somewhat sour to bittersweet. As a result of continued cross-breeding, the essential oil's fragrance, like the taste of the fruit, has become 'softer' and with less character than in the past. The grapefruit scent note blends especially well with bergamot, mandarin, neroli, basil, frankincense, peppermint, rosemary, chamomile, clove, black pepper, nutmeg, fennel, ginger, lavender, oakmoss, cypress, cedarwood, rosewood, balsam, juniper, geranium, jasmine, patchouli, and ylang-ylang. The oil breaks down on the skin to form somewhat malodorous compounds, so fruit ester 'modifiers' are sometimes added to it to maintain a fresher floral scent after application.

Grapefruit has a long history of use in folk medicines around the world and has been used traditionally as an antibacterial, antifungal, anti-inflammatory, antioxidant, astringent, and preservative. It is has popular as a remedy for cellulite and as an antidepressant. In aromatherapy, it is thought to be calming but stimulating and uplifting. It is also used commercially as a flavoring agent in foods and beverages and as a fragrance ingredient in soaps, detergents, and personal care products.

Masculine grapefruit fragrances:

Acqua di Gio Essenza
Agonist Solaris
Alfred Dunhill X-Centric
Alendor Taboo
Antonio Puig Quorum
Aramis Havana
Atelier Cologne Pomelo Paradis
Athena Vetiver
Autre Parfum Avant-Garde
Azzaro Chrome (various), Azzaro Jetlag, Azzaro LE 2016
Baldessarini Del Mar Marbella
Barbour
Benetton White Night
Bvlgari Aqua Marine, Bvlgari Man Extreme, Bvlgari Tygar
Burberry Mr. Burberry, Burberry Sport, Burberry Weekend
By Killian Smoke for the Soul
Carolina Herrera 212 Summer 2013, CH 212 Surf, CH Sport
Cacharel Amor Sunshine
Cartier Declaration l'Eau
Chanel Bleu
Chopard Malaki
Christian Dior Aqua Fahrenheit, CD Higher Energy, CD Homme Sport, CD Vetiver
Creed Himalaya
Davidoff Good Life
Dolce & Gabbana Light Blue, D&G The One
Dzintars Sudrabotais Ledus Blue
Emanuel Ungaro Fresh
Estee Lauder Pleasures
Fiorucci Extreme Sport
Giorgio Armani Night
Giorgio Beverly Hills Ocean Dream
Givenchy Blue Label, Givenchy Fresh Attitude
Guerlain Aqua Allegoria Pamplelune, Guerlain l'Instant
Guy Laroche Drakkar Dynamik
Hermes Terre d'Hermes
Hugo Boss Boss in Motion, HB Boss Pure, HB Boss Selection, HB Boss Unlimited, HB Hugo Dark Blue
I-Scents Premium Blue Concept
Issey Miyake Sport Polar Expedition
Jacques Bogart Riviera Nights
Jean Paul Gaultier Le Male Terrible
Jeanne Arthes Joe Sorrento Sport
Jequiti Abyssal Homem Energy
Jo Malone Grapefruit
Kenzo Fresh
Korres Neos
Lange Orient Treasure
Loewe Sport Edicion Especial
Louis Cardin La Viola
Mont Blanc Emblem
Moschino Forever Sailing
Oriflame Ascendant Aqua, Oriflame Eclat Lui
Paco Rabanne 1 Million, PR Invictus
Paul Sebastian Silver
Paul Smith Sunshine Edition
Sean John Unforgivable Night
Tom Ford Mandarino di Amalfi
Tommy Hilfiger Freedom, TH True Star
Victorio & Lucchino No7 Frescor Mediterraneo
Viktor & Rolf Spicebomb
Yves Rocher Cypres et Pamplemousse
Zara Denim Couture, Zara Navy Black, Zara Norrland, Zara Vibrant Leather Parfum de Liberte

Pink grapefruit fragrances for men (generally sweeter):

Bvlgari Man Extreme (various)
Carolina Herrera 212 NYC Seductive
Cartier Declaration l'Eau
Emanuel Ungaro Cologne Extreme
Il Profvmo Cafe Vert
Karl Lagerfeld Bois de Vetiver
Kenzo Electric Wave
Kanon Kool
Lacoste Essential Sport
Nautica Gold Rush
Ralph Lauren Big Pony 4, RL Polo Red (various)
S.T. Dupont Paris by Night
Tommy Hilfiger Eau de Prep, TH Hilfiger
Van Gils Strictly for Night
Yohji Yamamoto His Love Story
Zara Black Edition
My favorite of the citrus scents! The cologne that I have that has the most realistic grapefruit note is Dolce & Gabbana Light Blue Forever
 
Galbanum

Galbanum is a gum resin, collected from several species of flowering Ferula plants, whose oil has a pungent, bitter, green, woody-resinous odor reminiscent of sliced green peppers and cut grass. It provides a "green" and somewhat earthy note to fragrance products. Galbanum frequently is mentioned as a top note, but its tenacity actually lingers in the heart and base. As it evolves on the skin, the initial acrid, peculiar scent is followed by a complex green, spicy tone, and then a woody-balsamic tone, after which it finally becomes more musky. It frequently is used in the creation of tobacco aromas. When employed as a base note, it usually is combined with musk, oakmoss, or pine. Traditionally it mainly has been used to give a natural green effect to floral accords, usually featuring hyacinth, gardenia, narcissus, iris, and violet, with which it pairs very well. Modern (post-1920s) "green" fragrances evoke the outdoors and nature much more than the sophisticated intimacy and animal density of more traditional chypres. Nevertheless, galbanum is also clearly present in many oriental blends, chypres, and fougeres as well. Galbanum resin also is prized for its fixative qualities; like other heavy molecules with low volatility, it anchors more ephemeral elements.

The Ferula plants from which galbanum is obtained originally grew in Mesopotamia and subsequently were exported to India, China, Israel, and Egypt. Today Iran and Turkey are the primary sources for galbanum. Galbanum also is produced in South Africa, Lebanon, southern Russia, and Afghanistan.

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The oil, the form most widely used in perfumery, is steam-distilled from the resinoid - a thick, crumbling, yellowish to greenish-brown paste - which is exuded from wounds cut in the trunks and roots of the plants.

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Initially the resin is earthy and peaty, but with dilution in alcohol the fruity-floral "bouquet" opens up, and one is reminded of crushed pine needles or pea pods with lemony overtones, fresh, vegetal, and sharp. The chemical constituents of galbanum are monoterpenes (a and ß pinene), sabinene, limonene, undecatriene and pyrazines. The pure oil, however, often is adulterated with pine oil, which may be why some batches of imports smell more of green, snapped pine needles than others. Perfume houses sometimes use additional steps beyond distillation to remove acrid sulfuric and terpenic notes when they are present.

The use of galbanum in perfumes is typified by Chanel No 19, Balmain Vent Vert, Guerlain Chamade, and Estée Lauder Aliage. It is also prominent in Robert Piguet Bandit, and it appears in Serge Lutens Iris Silver Mist, Atelier Cologne Grand Néroli, and Guerlain La Petite Robe Noire Modèle 2.

Galbanum also has been used as a medicinal ingredient, primarily as an anti-inflammatory agent, expectorant, and antiseptic, and as an antispasmodic for women during childbirth. In ancient Egypt it was burned in incense in religious ceremonies and was used in embalming processes.

Fragrances for men or both genders that feature galbanum include:

Penhaligon's Quercus
Creed Silver Mountain Water, Royal Oud, Cedre Blanc, Iris Tuberose
Czech & Speake Vétiver Vert
Hugo Boss Red
Ineke Hothouse Flower
L'Artisan Parfumeur Premier Figuier
Olfactive Studio Panorama, Still Life
Police Naked pour Homme
Versace Blue Jeans for Men
Hareer Anfasic Dokhoon
Pioneer Boadicea the Victorious
Lush Flower Market
Etienne Aigner Private Number
Pino Silvestre Green Generation
Black Phoenix Alchemy Lab Dragon's Eye
Tom Ford Vert de Fleur, Vert Bohème, Ombre de Hyacinth
Chanel Egoiste Platinum
Wax Poetic Ember
Jeanne Arthes Cobra pour Homme
Emper Bandit, Presidente Sports
Serge Lutens Bas de Soie, Borneo 1834
Maison Martin Margiela (untitled)
Comme des Garcons
Cartier Must pour Homme
Miller Harris Patchouli
Testa Maura Carticasi
Anglia Perfumery Park Royal
Vilhelm Parfumerie Morning Chess
Dolce & Gabbana Velvet Vetiver
Jequiti Aire
Aramis Devin
Phaedon Coton Egyptien
Ava Luxe Figuer
Fueguia 1833 Gálbano
O Boticario Uomini
Gap Established 1969
Esprit de Versailles for Him
Officina delle Essenze Caldo Encens
Swiss Arabian Shadha
Zoologist Macaque
Monsillage Eau de Céleri
Novaya Zarya Driver
Acqua di Stresa Dianthus
Prada No 8 Opopanax, Infusion d'Homme
Ralph Lauren Safari
Guepard for Man
Dina Cosmetics Imperial Silver Black
DSH Perfumes Adoration (Milan), Viridian
Renato Balestra Via Sistina 67 Homme
D.S. & Durga Sir
Laura Biagiotti Roma per Uomo
Azzaro Aqua Verde
Art Deco Perfumes Aventure
Anatole Lebreton l'Eau de Merzhin
Geoffrey Beene Grey Flannel
Maitre Parfumeur et Gantier Eau des Iles
Frederic Malle French Lover
 
Fragrance Classification and Fragrance Wheels

In perfumery there have been four main fragrance categories traditionally: Fresh, Floral, Oriental, and Woody. Within these four main groups fall generally accepted families; and beyond these are numerous combinations of notes that blur the lines of distinction.

The original classification of fragrances, which emerged around 1900, consisted of 7 entities:

•Single floral: dominated by a scent from one particular flower, in French called a soliflore.
•Floral bouquet: containing a combination of several flowers in a scent.
•Ambery or oriental: sweet, spicy, and exotic, featuring vanilla and animal scents together with flowers, woods, and spices such as cardamom and clove, sometimes enhanced by camphoraceous oils and incense resins.
•Woody: dominated by wood scents, typically of sandalwood, oak, and cedar. Patchouli is commonly found in these perfumes.
•Leather: featuring the scents of honey, tobacco, wood and wood tars in the middle or base notes and suggesting leather items.
•Chypre: fragrances built on an accord consisting of bergamot, oakmoss, patchouli, and labdanum. Named after a perfume by Francois Coty.
•Fougère: having a base of lavender, coumarin, and oakmoss and characterized by a sharp herbaceous and woody scent.

Since 1945, due to technological advances in compound design and synthesis and to style evolution, additional categories of scents have emerged:
•Bright floral: combining the traditional Single floral and floral bouquet categories.
•Green: a lighter and more modern interpretation of the chypre type.
•Oceanic/Aquatic/Ozone: the newest category, appearing in 1991, a clean, modern smell invoking the sea or the smell of rain, and leading to many of the modern androgynous perfumes.
•Citrus or Fruity: a very old fragrance family that until recently consisted mainly of "freshening" eau de colognes due to the low tenacity of natural citrus scents such as lemon, orange, bergamot, grapefruit, and mandarin. Development of newer fragrance compounds has allowed for the creation of stabel primarily citrus fragrances.
•Gourmand: scents with "edible" or "dessert"-like qualities, often containing notes like vanilla and tonka bean, as well as synthetic components designed to resemble food flavors.

However, there is not a complete consensus, and according to some experts, there should be eight major families: four feminine ones (Chypre, Floral, feminine Citrus, and feminine Oriental) and four masculine ones (Aromatic, Woody, masculine Citrus, and masculine Oriental).


Fragrance Wheel

The Fragrance wheel (or aroma wheel, fragrance circle, perfume wheel) is a relatively new classification method that is widely used in the fragrance industry. It is represented by a round diagram. The method was first used in 1949 by Austrian perfumer Paul Jellinek and was titled the Odor Effects Diagram:

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Subsequently U. Harder at Haarman & Reimer and others developed several variations of the Fragrance Circle. And in 1983 Michael Edwards, a consultant in the perfume industry, designed his own scheme of fragrance classification after being inspired by a fragrance seminar by Firmenich. Since its creation, Edwards' wheel has been modified several times, and it is the most widely used model.

The wheel scheme first was created in order to simplify fragrance classification and naming on a logical basis, as well as to show the relationships between individual classes, based upon odor similarities and differences, which previous classifications had overlooked.

The five standard families on most wheels now consist of Floral, Oriental, Woody, Fougère, and Fresh, with the first four families being the more "classic" ones, while the Fresh category consists of newer, bright and clean-smelling citrus and oceanic fragrances that have arrived due to improvements in fragrance technology. With the exception of the Fougères, each of the families is in turn usually divided into three sub-groups and arranged around a wheel:

1. Floral

1.Floral - notes of fresh-cut flowers
2.Soft Floral - aldehydes and powdery notes
3.Floral Oriental - main notes of orange blossom and sweet spices

2. Oriental

1.Soft Oriental - incense and amber
2.Oriental - vanilla and oriental resins such as frankincense
3.Woody Oriental - sandalwood and patchouli

3. Woody

1.Woods (added 2008) - aromatic woods and vetiver
2.Mossy Woods - oakmoss and amber
3.Dry Woods - dry woods and leather

4. Fresh

1.Citrus - bergamot and citrus oils
2.Green - galbanum and green notes
3.Water (Oceanic/Aquatic) - marine and aquatic notes, especially from calone
(4.Fruity - added 2008) - berries and other non-citrus fruits

5. Aromatic/Fougère


The idea is that the wheel represents the circular continuum of fragrances which humans can perceive, with each group blending into and overlapping with its two neighbors, with implied common olfactory characteristics. For instance Floral Oriental scents consist of a mingling of florals with sweet and spicy notes, while the adjacent Soft Oriental group frequently includes a slight flowery touch.

Until recently, the Fougère family was placed at the center of the wheel since it takes fragrance elements from the other four families, citrus from the Fresh, oakmoss and woods from Woody, coumarin and incense from Oriental, and lavender from Floral. This is shown in the 1983 wheel:

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With a further modification in 2010, the Aromatics/Fougère group was moved to a space between Dry Woods and Citrus to synchronize the chart with newer studies of smell perception, and in some charts it actually is included under the Woody class. The 2010 Edwards chart:

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In order to differentiate further, some experts have divided each of a family's subclasses in turn into Fresh, Crisp, Classical, or Rich compositions, while others have simply divided a subclass further into the individual scents themselves.

As a class, Chypres is more difficult to place since it usually would be located under parts of the Oriental and Woody families. For instance, Guerlain Mitsouko, which is classically identified as a Chypre, would be placed under Mossy Woods, but Hermès Rouge, a Chypre with a more floral character, would be put under Floral Oriental. Attempts have been made to incorporate the Chypres into a chart scheme, such as that of the Lebermuth Company, which sets it between the Fougères and the Camphoraceous (eucalyptus, rosemary, and pine), in addition to showing the presumed relationships of individual scents:

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Another wheel example is that of the Chemia Corporation, which divides fragrances into different groups based upon their somewhat subjective predominant character, including "foodlike" ones, as shown here:

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Still another chart which differentiates more is the Atelier wheel:

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And the Drom Fragrance Circle further subjectively aligns scents with gender:

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A more recent chart, outlining aromachemical relationships rather than smell perceptions, is the non-circular Givaudan Scent Ingredients Map:

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And finally, some constructs attempt to express the recently well-described connection and cross-sensory interrelationship between the senses of smell and taste, such as the Aromaster chart:

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Despite these attempts at classification, individual perfume products often remain difficult to characterize objectively. Fragrances may share notes, accords, or other characteristics, but each perfume is an individual entity with unique notes. Because of this uniqueness, a perfume can be seen to fall into more than one category of fragrance, especially since it will have a different smell on one person than on someone else and will vary in its overall personality with body chemistry changes and with the passage of time.
 
Ginger

Ginger (Zingiber officinale) is an herbaceous reed-like plant whose fleshy rhizome, commonly called ginger root or just ginger, is used widely as a spice, a food or condiment, a source of fragrance, and a folk medicine. It is a perennial that grows to a height of about one meter and bears annual narrow-bladed leaves and white and pink buds that bloom into flowers with red or yellow petals, sometimes with purple edges. The plant arises directly from the underground rhizome on separate shoots. Ginger is in the family Zingiberaceae, which also includes turmeric, cardamom, and galangal.
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The English origin of the word 'ginger' is derived from the Sanskrit word 'srngaveram' by way of Prakrit, Greek, Latin, mid-14th century Old English, Old French, and finally Middle English. It is not clear what exactly the Sanskrit word meant, but it is thought that it may have described the shape of the root.

Origination and Spread

Native to India, Malaysia, and possibly China, ginger most likely was first domesticated by Austronesians (peoples from maritime southeast Asia, Micronesia, coastal New Guinea, island Melanesia, Polynesia, and Madagascar with a common language), who also cultivated turmeric. The rhizomes and leaves were eaten by them or used to flavor food, and the leaves were used for weaving mats and hangings. Ginger also had religious significance for the Austronesians and was used in rituals. They transported it throughout the Indo-Pacific during their expansion 5,000-3,500 years ago, eventually reaching as far as Hawaii. They presumably also introduced it to India, Madagascar, and the Comoros. From India it was carried by traders to the Middle East and the Mediterranean, along with peppers, cloves, and other spices, by around the 1st century. Ginger is one of the first spices to have been exported from Asia.
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The first written record of ginger comes from the Analects of Confucius, written in China sometime around 475-221 BC. In 406, the monk Faxian wrote that ginger was grown in pots and carried on Chinese ships for use to prevent scurvy. And there are records from the Song Dynasty (960-1279) showing that ginger was being imported into China. After its introduction to the Mediterranean by the Arabs, ginger was described by various Greek writers, including Ptolemy. It was also mentioned commonly by the Romans. By the Middle Ages, it was being imported into most of Europe, where it was described in the official pharmacopeias of several countries.

Growing, Harvesting, and Processing

Ginger is a true cultigen and no longer exists in its wild state. It is able to grow in a wide variety of land types and areas, but it is produced best when grown in a warm, humid environment at an elevation of 1,000-3,000 feet. A period of low rainfall prior to growing and well-distributed rainfall during growing are essential for it to thrive. In India, planting is usually done between March and June, at the beginning of the monsoon season. For fresh use as a vegetable or for candy, harvesting is done at 4-5 months after planting, whereas when the planting is done for dried ginger or ginger oil, harvesting must be done at 8-10 months. The older the plant gets, the more the root's scent dissipates, become only pungent. It most often is grown through homestead farming, with employees being family members or other local members of the community.
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The size of the seed rhizome determines plant production: the larger the rhizome piece, the faster a plant will be produced and available for sale on the market.
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Dried ginger (bleached or unbleached), one of the most popular forms exported commercially, must have its moisture content decreased from 80% to about 10%. The harvested rhizomes are soaked overnight and cleaned well by rubbing, after which the outer skin is scraped off with a bamboo splinter or wooden knife by hand in order to prevent sprouting. It is then allowed to sun-dry for 8-10 days (or is machine dried), graded, and hand 'polished' to remove dry skin and wrinkles. Ginger is sometimes bleached by repeated dipping in a slaked lime slurry, followed each time by drying; dry ginger can be bleached by a similar process. This liming gives the ginger a better appearance and less susceptibility to attack by insect pests during storage and shipping. When it arrives in terminal markets (eg New Delhi or Bombay) or the consuming country, the dried ginger is ground. The yield of dry ginger is about 20-25% by weight of the harvested fresh ginger.
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Commercial fresh (green) ginger is not dried this way. It is suitable for immediate fresh consumption or for processing into preserved, pickled, or candied ginger for sale or export. When marketed for consumption, it is usually eaten fresh in the area where it is produced, although it is possible to transport fresh roots internationally.
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In 2019, world production of ginger was 4.1 million tons, with India providing 44% of the total and substantial amounts from Nigeria, China, Brazil, and Japan. It is also grown in Nepal, the Caribbean, South America, and areas of Africa. A good deal of India's ginger is used domestically, and the country is only in seventh place in worldwide export of it, accounting for just 1-2% of total exports. Most of the world export of ginger comes from China.
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Perfumery

Ginger has been used in perfumery for several centuries, since the discovery of distillation. Its scent is considered woody and spicy, with fresh, contrasting sweet and bitter nuances. Ginger's odor profile includes a spicy, fizzy, 'rising' top note aspect, with a pronounced fresh lemony citrus facet as well as a piney, soapy nuance. The aroma is fresh and sparkling, but at the same time pungent and peppery. In compositions, it is usually used as a middle note, although it also appears at times among top notes. As a middle note it blends well with resinous scents such as frankincense or sandalwood and with woods (especially cedarwood, red cedar, and rosewood) and other spicy notes, such as cinnamon, cardamom, and black pepper. When used as a top note, it blends nicely with citruses (especially mandarin and lemon) and florals (especially rose, geranium, jasmine, and carnation, whose sweetness it balances). It also is paired sometimes with neroli, bergamot, lemongrass, lavender, mint, basil, vanilla, juniper, and patchouli. Although its presence usually can be sensed immediately, it develops throughout the evolution of a perfume product on the skin, often felt even until the base notes. Fragrances with ginger work well in both warmer and cooler weather. The scent can be found in both feminine and masculine preparations, although most commonly in the former.

Ginger essential oil for perfumery is produced through steam distillation or supercritical CO2 distillation of the rhizome. The modern use of CO2 distillation has revealed previously unknown aspects of the overall aroma. Spicy ginger perfumes were especially popular during the Renaissance, but gradually fell into temporary disfavor during the early 20th century. Thanks to the creativity of more modern noses, however, they have made a marked comeback, beginning with Shalimar in 1925.
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The characteristic fragrance of ginger results from volatile oils that make up 1-3% of the weight of the fresh rhizome, primarily consisting of sesquiterpenes such as zingerone, shogaols, and gingerols, with [6]-gingerol as the major aromatic compound. Gingerol is related to capsaicin and is one of the spicy components in chili peppers, albeit with low potency. Zingerone is produced from gingerols during the drying process and has lower pungency and a spicy-sweet aroma. Shogaols, formed from gingerols during heating or storage, are more pungent but maintain the same aroma. (This is why dried ginger powder adds more pungency than fresh ginger in cooking use.)
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Other Uses

Dried ginger is a common kitchen spice, used as a flavoring for items such as gingerbread, cookies and cakes, crackers, ginger ale, and ginger beer. Candied or crystallized ginger (the root cooked in sugar until soft) is a type of confectionery. Young fresh ginger rhizomes are juicy and have a mild taste, and they can be pickled in vinegar or sherry for use as a snack or as an ingredient in cooked dishes. They also can be steeped in boiling water to make hot or cold herbal teas or made into candy or ginger wine. The juice from fresh ginger roots is often used as a seasoning in Indian, Chinese, Korean, Japanese, and Vietnamese dishes.
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In the Caribbean, ginger is popular for use in cooking and for making drinks, such as sorrel during the Christmas season. Jamaicans make ginger beer, ginger tea, and a famous ginger cake. On the Greek island of Corfu, a type of ginger beer is made, adopted from the British. In Western cuisine, dried ginger is traditionally used mainly to flavor sweet foods, as well as being added to hot coffee or tea.

Ginger has had a role for centuries in traditional Ayurvedic medicine. It was thought to have antiseptic and immunity-boosting properties and has been reputed to promote the health of pregnant or nursing women. It also has had fame, especially in Europe, as a powerful aphrodisiac. In addition, it was consumed there in past centuries because it was thought to ward off the plague. There is some modern evidence for ginger having an anti-inflammatory effect and improving digestive function. A 2018 review found evidence that it could decrease body weight and increase HDL-cholesterol in obese subjects.

Because of its attractiveness and its adaptation to warmer climates, the ginger plant is often used for landscaping, especially around subtropical homes.

Masculine Fragrances with Ginger

Adolfo Dominguez Agua Fresca Citrus Cedro
Angel Schlesser Esprit de Gingembre pour Homme
Animale Black
Antonio Banderas Mediterraneo
Aramis Mustang
Avon Christian Lacroix Noir, Avon Free for Him, Avon Herve Leger Homme, Avon Up to You for Him
Azzaro pour Homme Ginger Lover, Azzaro Pure Cedrat, Azzaro Vibrant Leather, Azzaro Wanted
Balmain Monsieur
Banana Republic Slate
Beverly Hills Polo Club Titan
Bvlgari BLV pour Homme, Bvlgari Le Gemme Empyr, Bvlgari Tygar
Burberry Brit for Men, Burberry Sport for Men (var.)
Calvin Klein Euphoria Men (var.)
Carolina Herrera 212 Heroes, CH Ginger
Cartier Déclaration
Carven Shenandoah
Cerruti Si
Chanel Bleu de Chanel
Christian Dior Homme Sport (var.)
Comptoir Gingembre et Vetiver
Creed Tabarome, Creed Vetiver
Davidoff Run Wild
Dolce & Gabbana The One for Men
Ermenegildo Zegna Bourbon Vanilla
Erox Realm Men
Evaflor Whisky Homme Sport
Gucci Envy for Men
Guy Fox JP
Hermès
Hugo Boss Bottled Tonic, HB Element, HB The Scent, HB The Scent Absolute
Jean Paul Gaultier Le Male Tonique
John Varvatos Artisan Pure
Joop! Rococo for Men
Kenzo Once Upon a Time pour Homme
Lacoste L.12.12. Blanc Eau Fraîche for Him, Lacoste L.12.12. Energized
Lancome Hypnôse Homme
Louis Vuitton l'Immensité
Natura Homem
Nuancielo Ville
Oriflame I.D. Beats
Prada l'Homme Water Splash, Prada Infusion de Vetiver, Prada Luna Rossa Sport
Ralph Lauren Big Pony 3
Serge Lutens Five O'Clock au Gingembre
Thera Cosméticos Biblos, TC Drago
Tiffany Tiffany & Love for Him
Tom Ford for Men
Tommy Hilfiger Freedom, TH Summer 2021, TH Weekend Getaway
Valentino Uomo Born in Roma (var.)
Van Cleef & Arpels Zanzibar
Versace Black Jeans
Yanbal Solo
Yves Rocher Cyprès et Pamplemousse
Yves St. Laurent l'Homme, YSL l'Homme Ultime, YSL, Jazz Prestige, YSL Y Live
Zara Cologne, Z Midsummer Orange Zest, Z Night Skyline, Z Sport 6.0, Z Vibrant Leather Summer, Z Warm Black
Zirh
Zlatan Ibrahimovic Supreme pour Homme

There are many unisex fragrances with ginger.


White Ginger Lily

The white ginger lily (Hedychium coronarium, also commonly known as white ginger, Hawaiian white ginger, butterfly lily, or Indian garland flower), native to Asia, is a perennial flowering plant that is also in the ginger family Zingiberaceae. An upright plant that can reach 1-3m in height, it has long pointed leaves and heavily-scented white flowers with yellow bases. It typically grows in the forest understory, where pseudostems arise from underground rhizomes. It is native to the eastern Himalayas of India, Bangladesh, Nepal, and Bhutan; through northern Myanmar and Thailand and southern China; and east to Taiwan. It was transported and naturalized widely, to Hawaii, southern Africa, eastern Australia, Central and South America, and the Caribbean. It became the national flower of Cuba, known there as mariposa blanca ('white butterfly') due to its shape. In Hawaii it has been used commonly for making leis for visitors. White ginger is cultivated primarily as an ornamental, although it is also grown commercially in China for use in medicine and for production of an aromatic essential oil.
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The amber-colored oil or absolute of white ginger flower, obtained from steam or solvent distillation of the flowers and leaves, displays an intense fragrance. It has a fresh, sweet, tropical floral smell, with a ginger-like fruity undertone that is reminiscent of jasmine, tuberose, and gardenia. The floral sweetness is very rich and deep and has excellent tenacity. It is thought that the constituents responsible for most of the scent are linalool, methyl jasmonate, eugenols, cis-jasmone, beta-ionone, and lactones.

White ginger usually is used in feminine fragrances, but it can appear in some unisex compositions and even a few masculine ones. It is used in the middle and base notes. Its note blends well with jasmine, cassia, sandalwood, balsam of Peru, cinnamon lavender, styrax, myrrh, frankincense, ginger, orris, patchouli, vanilla, and ylang-ylang.

Masculine Fragrances with White Ginger

Abercrombie & Fitch Intense.
Escada Moon Sparkle pour Homme

Unisex White Ginger Compositions

Amberfig Pluie d'Orange
CB I Hate Perfume White Ginger
Dame Soliflore Ginger Lily
Fragrenza Rame Verde
Hermès Un Jardin Apres la Mousson
Liana of Waikiki White Ginger
Louis Marie No.12 Bousval
Magnetic Scent Untitled 1
Olympic Orchids Kilauea
Persephenie White Ginger Lily
Phebo Flor de Maio
Phoenix Ka Pueo
PK Ginger Zest de Citron
Régime des Fleurs Leis
Renier De Lirius
Sarah Jessica Parker Stash SJP
Sultan Pasha Attars Jardin de Borneo White Ginger Lily
TRNP Blossom, TRNP East, TRNP Oasis, TRNP La Selva Sagrada
 
Ginger

Ginger (Zingiber officinale) is an herbaceous reed-like plant whose fleshy rhizome, commonly called ginger root or just ginger, is used widely as a spice, a food or condiment, a source of fragrance, and a folk medicine. It is a perennial that grows to a height of about one meter and bears annual narrow-bladed leaves and white and pink buds that bloom into flowers with red or yellow petals, sometimes with purple edges. The plant arises directly from the underground rhizome on separate shoots. Ginger is in the family Zingiberaceae, which also includes turmeric, cardamom, and galangal.
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gRL7mwH.jpg
sE9Ofqg.jpg
SJ56eeS.jpg


The English origin of the word 'ginger' is derived from the Sanskrit word 'srngaveram' by way of Prakrit, Greek, Latin, mid-14th century Old English, Old French, and finally Middle English. It is not clear what exactly the Sanskrit word meant, but it is thought that it may have described the shape of the root.

Origination and Spread

Native to India, Malaysia, and possibly China, ginger most likely was first domesticated by Austronesians (peoples from maritime southeast Asia, Micronesia, coastal New Guinea, island Melanesia, Polynesia, and Madagascar with a common language), who also cultivated turmeric. The rhizomes and leaves were eaten by them or used to flavor food, and the leaves were used for weaving mats and hangings. Ginger also had religious significance for the Austronesians and was used in rituals. They transported it throughout the Indo-Pacific during their expansion 5,000-3,500 years ago, eventually reaching as far as Hawaii. They presumably also introduced it to India, Madagascar, and the Comoros. From India it was carried by traders to the Middle East and the Mediterranean, along with peppers, cloves, and other spices, by around the 1st century. Ginger is one of the first spices to have been exported from Asia.
l62bSpN.jpg


The first written record of ginger comes from the Analects of Confucius, written in China sometime around 475-221 BC. In 406, the monk Faxian wrote that ginger was grown in pots and carried on Chinese ships for use to prevent scurvy. And there are records from the Song Dynasty (960-1279) showing that ginger was being imported into China. After its introduction to the Mediterranean by the Arabs, ginger was described by various Greek writers, including Ptolemy. It was also mentioned commonly by the Romans. By the Middle Ages, it was being imported into most of Europe, where it was described in the official pharmacopeias of several countries.

Growing, Harvesting, and Processing

Ginger is a true cultigen and no longer exists in its wild state. It is able to grow in a wide variety of land types and areas, but it is produced best when grown in a warm, humid environment at an elevation of 1,000-3,000 feet. A period of low rainfall prior to growing and well-distributed rainfall during growing are essential for it to thrive. In India, planting is usually done between March and June, at the beginning of the monsoon season. For fresh use as a vegetable or for candy, harvesting is done at 4-5 months after planting, whereas when the planting is done for dried ginger or ginger oil, harvesting must be done at 8-10 months. The older the plant gets, the more the root's scent dissipates, become only pungent. It most often is grown through homestead farming, with employees being family members or other local members of the community.
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The size of the seed rhizome determines plant production: the larger the rhizome piece, the faster a plant will be produced and available for sale on the market.
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Dried ginger (bleached or unbleached), one of the most popular forms exported commercially, must have its moisture content decreased from 80% to about 10%. The harvested rhizomes are soaked overnight and cleaned well by rubbing, after which the outer skin is scraped off with a bamboo splinter or wooden knife by hand in order to prevent sprouting. It is then allowed to sun-dry for 8-10 days (or is machine dried), graded, and hand 'polished' to remove dry skin and wrinkles. Ginger is sometimes bleached by repeated dipping in a slaked lime slurry, followed each time by drying; dry ginger can be bleached by a similar process. This liming gives the ginger a better appearance and less susceptibility to attack by insect pests during storage and shipping. When it arrives in terminal markets (eg New Delhi or Bombay) or the consuming country, the dried ginger is ground. The yield of dry ginger is about 20-25% by weight of the harvested fresh ginger.
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Commercial fresh (green) ginger is not dried this way. It is suitable for immediate fresh consumption or for processing into preserved, pickled, or candied ginger for sale or export. When marketed for consumption, it is usually eaten fresh in the area where it is produced, although it is possible to transport fresh roots internationally.
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In 2019, world production of ginger was 4.1 million tons, with India providing 44% of the total and substantial amounts from Nigeria, China, Brazil, and Japan. It is also grown in Nepal, the Caribbean, South America, and areas of Africa. A good deal of India's ginger is used domestically, and the country is only in seventh place in worldwide export of it, accounting for just 1-2% of total exports. Most of the world export of ginger comes from China.
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Perfumery

Ginger has been used in perfumery for several centuries, since the discovery of distillation. Its scent is considered woody and spicy, with fresh, contrasting sweet and bitter nuances. Ginger's odor profile includes a spicy, fizzy, 'rising' top note aspect, with a pronounced fresh lemony citrus facet as well as a piney, soapy nuance. The aroma is fresh and sparkling, but at the same time pungent and peppery. In compositions, it is usually used as a middle note, although it also appears at times among top notes. As a middle note it blends well with resinous scents such as frankincense or sandalwood and with woods (especially cedarwood, red cedar, and rosewood) and other spicy notes, such as cinnamon, cardamom, and black pepper. When used as a top note, it blends nicely with citruses (especially mandarin and lemon) and florals (especially rose, geranium, jasmine, and carnation, whose sweetness it balances). It also is paired sometimes with neroli, bergamot, lemongrass, lavender, mint, basil, vanilla, juniper, and patchouli. Although its presence usually can be sensed immediately, it develops throughout the evolution of a perfume product on the skin, often felt even until the base notes. Fragrances with ginger work well in both warmer and cooler weather. The scent can be found in both feminine and masculine preparations, although most commonly in the former.

Ginger essential oil for perfumery is produced through steam distillation or supercritical CO2 distillation of the rhizome. The modern use of CO2 distillation has revealed previously unknown aspects of the overall aroma. Spicy ginger perfumes were especially popular during the Renaissance, but gradually fell into temporary disfavor during the early 20th century. Thanks to the creativity of more modern noses, however, they have made a marked comeback, beginning with Shalimar in 1925.
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The characteristic fragrance of ginger results from volatile oils that make up 1-3% of the weight of the fresh rhizome, primarily consisting of sesquiterpenes such as zingerone, shogaols, and gingerols, with [6]-gingerol as the major aromatic compound. Gingerol is related to capsaicin and is one of the spicy components in chili peppers, albeit with low potency. Zingerone is produced from gingerols during the drying process and has lower pungency and a spicy-sweet aroma. Shogaols, formed from gingerols during heating or storage, are more pungent but maintain the same aroma. (This is why dried ginger powder adds more pungency than fresh ginger in cooking use.)
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Other Uses

Dried ginger is a common kitchen spice, used as a flavoring for items such as gingerbread, cookies and cakes, crackers, ginger ale, and ginger beer. Candied or crystallized ginger (the root cooked in sugar until soft) is a type of confectionery. Young fresh ginger rhizomes are juicy and have a mild taste, and they can be pickled in vinegar or sherry for use as a snack or as an ingredient in cooked dishes. They also can be steeped in boiling water to make hot or cold herbal teas or made into candy or ginger wine. The juice from fresh ginger roots is often used as a seasoning in Indian, Chinese, Korean, Japanese, and Vietnamese dishes.
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In the Caribbean, ginger is popular for use in cooking and for making drinks, such as sorrel during the Christmas season. Jamaicans make ginger beer, ginger tea, and a famous ginger cake. On the Greek island of Corfu, a type of ginger beer is made, adopted from the British. In Western cuisine, dried ginger is traditionally used mainly to flavor sweet foods, as well as being added to hot coffee or tea.

Ginger has had a role for centuries in traditional Ayurvedic medicine. It was thought to have antiseptic and immunity-boosting properties and has been reputed to promote the health of pregnant or nursing women. It also has had fame, especially in Europe, as a powerful aphrodisiac. In addition, it was consumed there in past centuries because it was thought to ward off the plague. There is some modern evidence for ginger having an anti-inflammatory effect and improving digestive function. A 2018 review found evidence that it could decrease body weight and increase HDL-cholesterol in obese subjects.

Because of its attractiveness and its adaptation to warmer climates, the ginger plant is often used for landscaping, especially around subtropical homes.

Masculine Fragrances with Ginger

Adolfo Dominguez Agua Fresca Citrus Cedro
Angel Schlesser Esprit de Gingembre pour Homme
Animale Black
Antonio Banderas Mediterraneo
Aramis Mustang
Avon Christian Lacroix Noir, Avon Free for Him, Avon Herve Leger Homme, Avon Up to You for Him
Azzaro pour Homme Ginger Lover, Azzaro Pure Cedrat, Azzaro Vibrant Leather, Azzaro Wanted
Balmain Monsieur
Banana Republic Slate
Beverly Hills Polo Club Titan
Bvlgari BLV pour Homme, Bvlgari Le Gemme Empyr, Bvlgari Tygar
Burberry Brit for Men, Burberry Sport for Men (var.)
Calvin Klein Euphoria Men (var.)
Carolina Herrera 212 Heroes, CH Ginger
Cartier Déclaration
Carven Shenandoah
Cerruti Si
Chanel Bleu de Chanel
Christian Dior Homme Sport (var.)
Comptoir Gingembre et Vetiver
Creed Tabarome, Creed Vetiver
Davidoff Run Wild
Dolce & Gabbana The One for Men
Ermenegildo Zegna Bourbon Vanilla
Erox Realm Men
Evaflor Whisky Homme Sport
Gucci Envy for Men
Guy Fox JP
Hermès
Hugo Boss Bottled Tonic, HB Element, HB The Scent, HB The Scent Absolute
Jean Paul Gaultier Le Male Tonique
John Varvatos Artisan Pure
Joop! Rococo for Men
Kenzo Once Upon a Time pour Homme
Lacoste L.12.12. Blanc Eau Fraîche for Him, Lacoste L.12.12. Energized
Lancome Hypnôse Homme
Louis Vuitton l'Immensité
Natura Homem
Nuancielo Ville
Oriflame I.D. Beats
Prada l'Homme Water Splash, Prada Infusion de Vetiver, Prada Luna Rossa Sport
Ralph Lauren Big Pony 3
Serge Lutens Five O'Clock au Gingembre
Thera Cosméticos Biblos, TC Drago
Tiffany Tiffany & Love for Him
Tom Ford for Men
Tommy Hilfiger Freedom, TH Summer 2021, TH Weekend Getaway
Valentino Uomo Born in Roma (var.)
Van Cleef & Arpels Zanzibar
Versace Black Jeans
Yanbal Solo
Yves Rocher Cyprès et Pamplemousse
Yves St. Laurent l'Homme, YSL l'Homme Ultime, YSL, Jazz Prestige, YSL Y Live
Zara Cologne, Z Midsummer Orange Zest, Z Night Skyline, Z Sport 6.0, Z Vibrant Leather Summer, Z Warm Black
Zirh
Zlatan Ibrahimovic Supreme pour Homme

There are many unisex fragrances with ginger.


White Ginger Lily

The white ginger lily (Hedychium coronarium, also commonly known as white ginger, Hawaiian white ginger, butterfly lily, or Indian garland flower), native to Asia, is a perennial flowering plant that is also in the ginger family Zingiberaceae. An upright plant that can reach 1-3m in height, it has long pointed leaves and heavily-scented white flowers with yellow bases. It typically grows in the forest understory, where pseudostems arise from underground rhizomes. It is native to the eastern Himalayas of India, Bangladesh, Nepal, and Bhutan; through northern Myanmar and Thailand and southern China; and east to Taiwan. It was transported and naturalized widely, to Hawaii, southern Africa, eastern Australia, Central and South America, and the Caribbean. It became the national flower of Cuba, known there as mariposa blanca ('white butterfly') due to its shape. In Hawaii it has been used commonly for making leis for visitors. White ginger is cultivated primarily as an ornamental, although it is also grown commercially in China for use in medicine and for production of an aromatic essential oil.
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The amber-colored oil or absolute of white ginger flower, obtained from steam or solvent distillation of the flowers and leaves, displays an intense fragrance. It has a fresh, sweet, tropical floral smell, with a ginger-like fruity undertone that is reminiscent of jasmine, tuberose, and gardenia. The floral sweetness is very rich and deep and has excellent tenacity. It is thought that the constituents responsible for most of the scent are linalool, methyl jasmonate, eugenols, cis-jasmone, beta-ionone, and lactones.

White ginger usually is used in feminine fragrances, but it can appear in some unisex compositions and even a few masculine ones. It is used in the middle and base notes. Its note blends well with jasmine, cassia, sandalwood, balsam of Peru, cinnamon lavender, styrax, myrrh, frankincense, ginger, orris, patchouli, vanilla, and ylang-ylang.

Masculine Fragrances with White Ginger

Abercrombie & Fitch Intense.
Escada Moon Sparkle pour Homme

Unisex White Ginger Compositions

Amberfig Pluie d'Orange
CB I Hate Perfume White Ginger
Dame Soliflore Ginger Lily
Fragrenza Rame Verde
Hermès Un Jardin Apres la Mousson
Liana of Waikiki White Ginger
Louis Marie No.12 Bousval
Magnetic Scent Untitled 1
Olympic Orchids Kilauea
Persephenie White Ginger Lily
Phebo Flor de Maio
Phoenix Ka Pueo
PK Ginger Zest de Citron
Régime des Fleurs Leis
Renier De Lirius
Sarah Jessica Parker Stash SJP
Sultan Pasha Attars Jardin de Borneo White Ginger Lily
TRNP Blossom, TRNP East, TRNP Oasis, TRNP La Selva Sagrada
Today’s shave for me is dedicated to Ginger
 
Lime

Lime is a citrus tree in the Rutaceae family. The tree seldom grows to more than 5m in height. Its branches spread and are irregular, with short twigs, small leaves, and many small spiny thorns. The smooth evergreen leaves are pale green. Small white flowers are produced, usually in clusters. The lemon-like fruit is usually 3-4cm in diameter, oval to nearly globular in shape, with a peel that is thin and greenish-yellow when the fruit is ripe. The pulp is tender, yellow-green in color, and quite acidic. Most limes have both more acid and more sugar than lemons, but a few varieties almost lacking citric acid are known as sweet limes. The fruit requires 5-6 months from flowering to harvest.
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There are several species of citrus trees whose fruits are called limes, including the Key lime or Mexican Lime (c. aurantifolia), Persian lime (c. latifolia), Makrut or Thai lime (C. hystrix), and desert lime. It is difficult to identify exactly which species of fruit are being called lime in different parts of the world, partially due to the botanical complexity of the citrus genus. Species of the genus hybridize readily, and only recently have genetic studies begun to illustrate the structures. The majority of cultivated species are hybrids, produced from the citron (C. medica), the mandarin orange (C. reticulata), the pomelo (C. maxima), and the micrantha (C. hystrix var. micrantha).
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For most commercial uses, two species are used, the Key lime and the Persian lime. The Key lime is used more for cocktails and pastries and in perfumery, while the larger and darker Persian lime is used mostly in perfumery.
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The name comes through French and Arabic from the Persian word līmū, meaning 'lemon.'

All citrus fruits likely appeared initially around 8 million years ago in the Himalayan foothills of eastern Assam, northern Myanmar, and western Yunnan. When the climate changed, bringing weaker monsoons and drier weather, the plants were able to spread throughout southeast Asia. Recent genetic studies suggest an origin for C. aurantifolia, the true lime now known as the Mexican or Key lime, in Malaysia. Molecular data indicate that this lime's female parent was C. micrantha, native to the Philippines; and the male parents was C. medica, a juiceless citron that was the first cultivated citrus and probably came from India or New Guinea.

Lime trees were spread throughout the world via migration and trade. The makrut lime, in particular, was one of the earliest citrus fruits introduced to other parts of the world by humans, spread into Micronesia and Polynesia through the Austronesian expansion (c. 200-1500 BCE) and taken to the Middle East and the Mediterranean region via the spice and incense trade routes by around 1200 BCE. Atiphanes said in the 4th century that citrus had reached Greece from Persia by then, and ancient Rome was known to have limes, as well as lemons and citrons.

Limes were introduced to western European countries by the Moors and by returning Crusaders in the 12th and 13th centuries. Subsequently, Christopher Columbus took lime seeds to the West Indies in 1493. Other Spanish and Portuguese explorers probably also transported it to the Americas, and the trees soon became widely distributed in the Caribbean and in Mexico and Florida. The Spanish introduced commercial lime cultivation to their West Indies colonies in the 16th century.
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During the 19th century, British sailors were issued a daily allowance of citrus, including lime, to prevent scurvy; the ships were provisioned with fruit from their colonies of Antigua and Barbados. Limes were preferred over lemons because they were less susceptible to fermentation, and the juice could be preserved with 15% rum. Thus the sailors acquired the nickname 'Limey.'
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Commercial lime growing reached south Florida during the 1830s, with groves initially planted in natural and blasted potholes in the limestone bedrock. A Caribbean area 'Lime Juice Cordial' industry was launched in the 1860s when a method for preserving lime juice with sulfur dioxide was discovered. Limes were crushed between rollers at sugar cane mills, and the juice was decanted into wooden vats and allowed to settle. After two weeks, clear juice was drawn off, sweetened with sugar, treated with S02, and sealed in casks. A similar process is still used today, with current techniques including the addition of calcium carbonate to shorten the settling time, sweetening done with cane syrup, and the juice pasteurized before bottling.

Limes are grown commercially and produce fruit year-round, primarily in tropical and subtropical regions. The Persian lime is the most common, although the smaller Key lime or Mexican lime is also economically important.
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World production of limes (combined with lemons for reporting) was 19.4 million tons. The top producing countries - Mexico, India, China, Argentina, Brazil, and Turkey - accounted for 65% of the total. Lime juice mainly comes from Mexico, Peru, Haiti, and Brazil.

Lime Essential Oil
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Lime oil, mainly from the peel of the fruit, is processed mainly in the West Indies. It is obtained by manual or machine pressing (cold expression) and by steam distillation, the only citrus fruit processed in both ways. When machinery is used to press the entire fruit, the oil is separated from the juice with a centrifuge. (Sometimes the juice-oil slurry is sent on to a steam distillation unit.) Expressed oil has a full-bodied, green, spicy, woodsy aroma with sweet, lactonic undertones. It features much less of the characteristic citrusy limonene molecule than other citrus oils. It is given its woodsy-coniferous character by pinenes and a slightly medicinal-green aspect by 1,8-cineole, the main aroma constituent in Eucalyptus. It also contains methyl anthranilate, a grape-wintergreen molecule that also occurs in many white flowers, as well as coumarin, which gives it a coconut finish. The expressed oil is pale yellow, light olive, or even dark green in color.
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Steam-distilled oil is produced either from the juice of the unripe fruit or from the crushed peels. The Mexican or Key lime is the main type used in distillation. The juice that is distilled comes into contact with steam for about 10 hours, reducing the citral content and producing alpha-terpineol (up to 7%). Distillation not only is cheaper, but also preferred for producing oil used in flavoring because it removes some of the characteristic bitterness and 'dry mouth' feeel that expressed oil has. The terpineol gives it sharpness, and its sweeter character is due to aliphatic aldehydes, with freshness provided by limonene. Most people prefer the distilled lime oil because it a smell more familiar and similar to that of all the lime-flavored products to which everyone is exposed through soft drinks and candies. Distilled oil is clear to pale yellow in color.
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Both types of oil become less sweet during dry-down, evolving into more woodiness.

Pressed oil, preferred for having greater tenacity and complexity, and being closest in aroma to the fresh fruit, is produced in much smaller quantities than distilled oil and is much more expensive. It is produced primarily in the West Indies and on the islands of Grenada and Montserrat.

Use in Perfumery

Lime's scent note is sharp, fresh, zesty, vibrant, lively, green, and slightly woody. The odor is dryer, fresher, lighter, and sweeter than that of lemon. It is uplifting, sparkling, and stimulating, and it gives an exotic accent, especially when combined with neroli in cologne and chypre compositions and aldehydic perfumes. It is described by some as having Coca-cola and sour candy nuances. It is more striking than other citrus notes such as bergamot, lemon, orange, and mandarin, but it is very often blended with them. It usually appears as an intense top note, adding clarity and enhancing freshness. Other top notes can sometimes be too sweet, and lime is added to 'break' them. Lime is used to boost and refresh other top notes in oriental fragrances and to bring freshness to exotic floral compositions, especially those with cyclamen, lily, ylang-ylang, frangipani, and rose. It is often used in fougeres, adding an extra bit of coumarin. Lime blends well with citronella, clary sage, lavender, lemongrass, and rosemary.

The note also is present in mojito accords (mint, rum, and lime), such as that of Guerlain Homme, and it is combined and blends well with vanilla and coconut in tropical compositions. Lime actually blends well with members of all the olfactory families; it is most often associated with fresh perfumes such as eau fraîche. It is thought to have appeared first in commercial fragrances around 1800-1810.

Lime is found in many masculine fragrances, where its woodsy tone blends well with the typical wood bases. It is not just used in summer compositions; it adds lightness, sweetness, and intensity to fragrances for all seasons. Perfumer Julie Massé describes it as 'a fantastically juicy, tart, citrus note. When you smell it in a fragrance, you can almost feel it smarting on your tongue...'

Kitchen Use

In cookery, lime is useful both for its acidity and for the floral aroma of its zest. It is a common ingredient in the cuisine of many cultures, especially Mexican, Vietnamese, Thai, Iraqi (Persian), and eastern Arabian, frequently used along with mint to season rice and raw vegetables. Lime pickles and lime chutney are important parts of Indian cuisine.

Lime juice, especially that of C. aurantifolia, is used to flavor drinks, foods (such as salad dressings and baked goods), candy, and gum; and it may be concentrated, dried, frozen, or canned. It is one of the main components of Coca-Cola and citrus-flavored sodas (ginger ale, 7-Up, and others). Key lime gives a characteristic flavor to desserts, including Key lime pie; and in Australia, desert lime is used to make marmalade.
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Lime juice may be squeezed from fresh limes or purchased in bottles in both unsweetened and sweetened forms. It is used to make limeade and as an ingredient in many cocktails.

Other Uses

Lime extracts and essential oils are often used in cleaning products, as well as in aromatherapy, often blended with pine and/or lemon oils. Citrate of lime and citric acid are also prepared from the fruit and are used for many commercial purposes. Lime is used often in saunas in combination with eucalyptus, where it is thought to cleanse the skin.
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Lime is thought to have antispasmodic, anti-inflammatory, and sedative properties, and it has been used in a variety of folk medicine traditions, but modern evidence is scant. It has been used for centuries in Indian Tantric rituals to ward off evil spirits.

Adverse Reactions

Contact with lime peel, juice, or cold-pressed essential oil, followed by exposure to sunlight or ultraviolet light, may cause a rash called phytophotodermatitis. This appears to be due to furanocoumarin compounds, especially bergapten. The peel contains higher concentrations of the chemicals than the pulp and so is significantly more phototoxic. Distilled lime oil does not cause this reaction.
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Masculine fragrances with significant lime:
(starred items are consensus favorites)

4711 Acqua Colonia Lime & Nutmeg*
Ajmal Titanium
Anglia Imperial Lime, Anglia Spiced Limes
Aramis Always, Aramis Cool Blend, Aramis Tuscany
l'Artisan Parfumeur Batucada
Atelier Cologne Cedrat Enivrant*
Axe Recover
Ayala Moriel ArbitRary
Azzaro Ginger Lover, Azzaro pour Homme Cologne Intense, Azzaro Travelling, Azzaro Wanted Tonic
Bath House Cuban Cedar & Lime
Bond No 9 Coney Island, Bond No 9 I Love New York for Fathers
Boucheron Jaipur
Burberry Bris Summer 2012, Burberry Summer 2009
Calvin Klein Obsession
Carolina Herrera VIP Men (var.)
Carven Prague
Christian Dior Eau Sauvage
Clive Christian 1872
Clubman Pinaud Lime Sec*
Coach Blue
Coty Stetson (var.)
Crabtree & Evelyn West Indian Lime
Creed Virgin Island Water*
Crown Spiced Limes
DS & Durga Barbados, DS&D Burning Barbershop
Geo. F. Trumper Extract of Limes
Giorgio Armani Acqua di Gio*
Guerlain Aqua Allegoria Limon Verde*, Guerlain Habit Rouge (var.), Guerlain Homme*, Guerlain Homme l'Eau Boisee*, Guerlain Vetiver
Floris Limes
Hermes Eau d'Orange Verte*
Hollister Free Wave
Issey Miyake Nuit d'Issey Bleu Astral*
Kenzo Aquadisiac
Lacoste Live
Lancome Trophee
Liz Claiborne Bora Bora*
Masaki Matsushima Aqua Mat
Montale Aoud Lime*
Montblanc Legend SE 2014
Odore Mio Fresh Lime
Oriflame Paradise
Pecksniff's Active
Penhaligon's Blenheim Bouquet*
Perry Ellis 360 Degrees Red
Pino Silvestre Modern Dandy
Ralph Lauren Big Pony 1, RL Chaps
Rasasi Chastity
Royal Barber Silver Razor
Royal Copenhagen 1775 Classic
Royall Lyme Bermuda Royall Lyme*
Shulton Old Spice Lime
Taylor of Old Bond Street No 74*
Tommy Bahama Set Sail St. Barts*
Tommy Hilfiger Citrus Brights, TH T
Truefitt & Hill Sandalwood, T&H West Indian Lime
Versace Baby Blue Jeans
Yardley Gold
Yves Rocher Antarctic, YR Bois de Cedre et Citron Vert, YR Comme Une Evidence Green
Zara Silver
Zirh

Limetta

Limetta (aka sweet lime, sweet lemon, sweet limetta, mousambi), considered to be a hybrid between bitter orange and citron, is also used in perfumery. It has a fine citrus scent reminiscent of lime but less acidic and slightly sweeter. One masculine fragrance with limetta is Sybarite Spicy Calabria.
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Finger Lime (C. australasica)

The finger lime (sometimes called caviar lime or caviar lemon) is a shrub or small tree of lowland tropical rainforest in the coastal border area of Queensland and New South Wales, Australia. Its oil is used in perfumery and has a fresh, sweet, clean, citrus fragrance with balsamic coumarin undertones. Masculine fragrances with finger lime include Jimmy Choo Urban Hero, Lacoste L.12.12 EdP Blanc, and Perry Ellis Bold Red.
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Kaffir Lime (c. hystrix)

The Kaffir lime or Makrut lime, including the leaves, is sometimes used in perfumery. Masculine compositions containing it include l'Bel 1200 Degrees C and Jequiti Azul.
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Mojito

Mojito is a fresh fantasy note reminiscent of the mojito drink (lime, mint, sometimes rum).
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Masculine fragrances said to have this note include:

Antonio Banderas Cocktail Seduction Blue
Calvin Klein CK One Shock Street Edition, CK Encounter Fresh
Caribbean Joe
Carolina Herrera 212 Men Pop!
David Beckham Beyond
Demeter Mojito (unisex)
Guerlain Homme
Masaki Matsuchima Mat;Stone
New Yorker Style Up
 
Lime

Lime is a citrus tree in the Rutaceae family. The tree seldom grows to more than 5m in height. Its branches spread and are irregular, with short twigs, small leaves, and many small spiny thorns. The smooth evergreen leaves are pale green. Small white flowers are produced, usually in clusters. The lemon-like fruit is usually 3-4cm in diameter, oval to nearly globular in shape, with a peel that is thin and greenish-yellow when the fruit is ripe. The pulp is tender, yellow-green in color, and quite acidic. Most limes have both more acid and more sugar than lemons, but a few varieties almost lacking citric acid are known as sweet limes. The fruit requires 5-6 months from flowering to harvest.
YuYAwEd.jpg
k1svGJv.jpg
vumlWiU.jpg


There are several species of citrus trees whose fruits are called limes, including the Key lime or Mexican Lime (c. aurantifolia), Persian lime (c. latifolia), Makrut or Thai lime (C. hystrix), and desert lime. It is difficult to identify exactly which species of fruit are being called lime in different parts of the world, partially due to the botanical complexity of the citrus genus. Species of the genus hybridize readily, and only recently have genetic studies begun to illustrate the structures. The majority of cultivated species are hybrids, produced from the citron (C. medica), the mandarin orange (C. reticulata), the pomelo (C. maxima), and the micrantha (C. hystrix var. micrantha).
e72Lv0R.jpg
0eDL5dV.jpg


For most commercial uses, two species are used, the Key lime and the Persian lime. The Key lime is used more for cocktails and pastries and in perfumery, while the larger and darker Persian lime is used mostly in perfumery.
c8Awjkg.jpg


The name comes through French and Arabic from the Persian word līmū, meaning 'lemon.'

All citrus fruits likely appeared initially around 8 million years ago in the Himalayan foothills of eastern Assam, northern Myanmar, and western Yunnan. When the climate changed, bringing weaker monsoons and drier weather, the plants were able to spread throughout southeast Asia. Recent genetic studies suggest an origin for C. aurantifolia, the true lime now known as the Mexican or Key lime, in Malaysia. Molecular data indicate that this lime's female parent was C. micrantha, native to the Philippines; and the male parents was C. medica, a juiceless citron that was the first cultivated citrus and probably came from India or New Guinea.

Lime trees were spread throughout the world via migration and trade. The makrut lime, in particular, was one of the earliest citrus fruits introduced to other parts of the world by humans, spread into Micronesia and Polynesia through the Austronesian expansion (c. 200-1500 BCE) and taken to the Middle East and the Mediterranean region via the spice and incense trade routes by around 1200 BCE. Atiphanes said in the 4th century that citrus had reached Greece from Persia by then, and ancient Rome was known to have limes, as well as lemons and citrons.

Limes were introduced to western European countries by the Moors and by returning Crusaders in the 12th and 13th centuries. Subsequently, Christopher Columbus took lime seeds to the West Indies in 1493. Other Spanish and Portuguese explorers probably also transported it to the Americas, and the trees soon became widely distributed in the Caribbean and in Mexico and Florida. The Spanish introduced commercial lime cultivation to their West Indies colonies in the 16th century.
UJBu1Da.jpg


During the 19th century, British sailors were issued a daily allowance of citrus, including lime, to prevent scurvy; the ships were provisioned with fruit from their colonies of Antigua and Barbados. Limes were preferred over lemons because they were less susceptible to fermentation, and the juice could be preserved with 15% rum. Thus the sailors acquired the nickname 'Limey.'
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Commercial lime growing reached south Florida during the 1830s, with groves initially planted in natural and blasted potholes in the limestone bedrock. A Caribbean area 'Lime Juice Cordial' industry was launched in the 1860s when a method for preserving lime juice with sulfur dioxide was discovered. Limes were crushed between rollers at sugar cane mills, and the juice was decanted into wooden vats and allowed to settle. After two weeks, clear juice was drawn off, sweetened with sugar, treated with S02, and sealed in casks. A similar process is still used today, with current techniques including the addition of calcium carbonate to shorten the settling time, sweetening done with cane syrup, and the juice pasteurized before bottling.

Limes are grown commercially and produce fruit year-round, primarily in tropical and subtropical regions. The Persian lime is the most common, although the smaller Key lime or Mexican lime is also economically important.
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World production of limes (combined with lemons for reporting) was 19.4 million tons. The top producing countries - Mexico, India, China, Argentina, Brazil, and Turkey - accounted for 65% of the total. Lime juice mainly comes from Mexico, Peru, Haiti, and Brazil.

Lime Essential Oil
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Lime oil, mainly from the peel of the fruit, is processed mainly in the West Indies. It is obtained by manual or machine pressing (cold expression) and by steam distillation, the only citrus fruit processed in both ways. When machinery is used to press the entire fruit, the oil is separated from the juice with a centrifuge. (Sometimes the juice-oil slurry is sent on to a steam distillation unit.) Expressed oil has a full-bodied, green, spicy, woodsy aroma with sweet, lactonic undertones. It features much less of the characteristic citrusy limonene molecule than other citrus oils. It is given its woodsy-coniferous character by pinenes and a slightly medicinal-green aspect by 1,8-cineole, the main aroma constituent in Eucalyptus. It also contains methyl anthranilate, a grape-wintergreen molecule that also occurs in many white flowers, as well as coumarin, which gives it a coconut finish. The expressed oil is pale yellow, light olive, or even dark green in color.
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Steam-distilled oil is produced either from the juice of the unripe fruit or from the crushed peels. The Mexican or Key lime is the main type used in distillation. The juice that is distilled comes into contact with steam for about 10 hours, reducing the citral content and producing alpha-terpineol (up to 7%). Distillation not only is cheaper, but also preferred for producing oil used in flavoring because it removes some of the characteristic bitterness and 'dry mouth' feeel that expressed oil has. The terpineol gives it sharpness, and its sweeter character is due to aliphatic aldehydes, with freshness provided by limonene. Most people prefer the distilled lime oil because it a smell more familiar and similar to that of all the lime-flavored products to which everyone is exposed through soft drinks and candies. Distilled oil is clear to pale yellow in color.
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Both types of oil become less sweet during dry-down, evolving into more woodiness.

Pressed oil, preferred for having greater tenacity and complexity, and being closest in aroma to the fresh fruit, is produced in much smaller quantities than distilled oil and is much more expensive. It is produced primarily in the West Indies and on the islands of Grenada and Montserrat.

Use in Perfumery

Lime's scent note is sharp, fresh, zesty, vibrant, lively, green, and slightly woody. The odor is dryer, fresher, lighter, and sweeter than that of lemon. It is uplifting, sparkling, and stimulating, and it gives an exotic accent, especially when combined with neroli in cologne and chypre compositions and aldehydic perfumes. It is described by some as having Coca-cola and sour candy nuances. It is more striking than other citrus notes such as bergamot, lemon, orange, and mandarin, but it is very often blended with them. It usually appears as an intense top note, adding clarity and enhancing freshness. Other top notes can sometimes be too sweet, and lime is added to 'break' them. Lime is used to boost and refresh other top notes in oriental fragrances and to bring freshness to exotic floral compositions, especially those with cyclamen, lily, ylang-ylang, frangipani, and rose. It is often used in fougeres, adding an extra bit of coumarin. Lime blends well with citronella, clary sage, lavender, lemongrass, and rosemary.

The note also is present in mojito accords (mint, rum, and lime), such as that of Guerlain Homme, and it is combined and blends well with vanilla and coconut in tropical compositions. Lime actually blends well with members of all the olfactory families; it is most often associated with fresh perfumes such as eau fraîche. It is thought to have appeared first in commercial fragrances around 1800-1810.

Lime is found in many masculine fragrances, where its woodsy tone blends well with the typical wood bases. It is not just used in summer compositions; it adds lightness, sweetness, and intensity to fragrances for all seasons. Perfumer Julie Massé describes it as 'a fantastically juicy, tart, citrus note. When you smell it in a fragrance, you can almost feel it smarting on your tongue...'

Kitchen Use

In cookery, lime is useful both for its acidity and for the floral aroma of its zest. It is a common ingredient in the cuisine of many cultures, especially Mexican, Vietnamese, Thai, Iraqi (Persian), and eastern Arabian, frequently used along with mint to season rice and raw vegetables. Lime pickles and lime chutney are important parts of Indian cuisine.

Lime juice, especially that of C. aurantifolia, is used to flavor drinks, foods (such as salad dressings and baked goods), candy, and gum; and it may be concentrated, dried, frozen, or canned. It is one of the main components of Coca-Cola and citrus-flavored sodas (ginger ale, 7-Up, and others). Key lime gives a characteristic flavor to desserts, including Key lime pie; and in Australia, desert lime is used to make marmalade.
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Lime juice may be squeezed from fresh limes or purchased in bottles in both unsweetened and sweetened forms. It is used to make limeade and as an ingredient in many cocktails.

Other Uses

Lime extracts and essential oils are often used in cleaning products, as well as in aromatherapy, often blended with pine and/or lemon oils. Citrate of lime and citric acid are also prepared from the fruit and are used for many commercial purposes. Lime is used often in saunas in combination with eucalyptus, where it is thought to cleanse the skin.
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Lime is thought to have antispasmodic, anti-inflammatory, and sedative properties, and it has been used in a variety of folk medicine traditions, but modern evidence is scant. It has been used for centuries in Indian Tantric rituals to ward off evil spirits.

Adverse Reactions

Contact with lime peel, juice, or cold-pressed essential oil, followed by exposure to sunlight or ultraviolet light, may cause a rash called phytophotodermatitis. This appears to be due to furanocoumarin compounds, especially bergapten. The peel contains higher concentrations of the chemicals than the pulp and so is significantly more phototoxic. Distilled lime oil does not cause this reaction.
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Masculine fragrances with significant lime:
(starred items are consensus favorites)

4711 Acqua Colonia Lime & Nutmeg*
Ajmal Titanium
Anglia Imperial Lime, Anglia Spiced Limes
Aramis Always, Aramis Cool Blend, Aramis Tuscany
l'Artisan Parfumeur Batucada
Atelier Cologne Cedrat Enivrant*
Axe Recover
Ayala Moriel ArbitRary
Azzaro Ginger Lover, Azzaro pour Homme Cologne Intense, Azzaro Travelling, Azzaro Wanted Tonic
Bath House Cuban Cedar & Lime
Bond No 9 Coney Island, Bond No 9 I Love New York for Fathers
Boucheron Jaipur
Burberry Bris Summer 2012, Burberry Summer 2009
Calvin Klein Obsession
Carolina Herrera VIP Men (var.)
Carven Prague
Christian Dior Eau Sauvage
Clive Christian 1872
Clubman Pinaud Lime Sec*
Coach Blue
Coty Stetson (var.)
Crabtree & Evelyn West Indian Lime
Creed Virgin Island Water*
Crown Spiced Limes
DS & Durga Barbados, DS&D Burning Barbershop
Geo. F. Trumper Extract of Limes
Giorgio Armani Acqua di Gio*
Guerlain Aqua Allegoria Limon Verde*, Guerlain Habit Rouge (var.), Guerlain Homme*, Guerlain Homme l'Eau Boisee*, Guerlain Vetiver
Floris Limes
Hermes Eau d'Orange Verte*
Hollister Free Wave
Issey Miyake Nuit d'Issey Bleu Astral*
Kenzo Aquadisiac
Lacoste Live
Lancome Trophee
Liz Claiborne Bora Bora*
Masaki Matsushima Aqua Mat
Montale Aoud Lime*
Montblanc Legend SE 2014
Odore Mio Fresh Lime
Oriflame Paradise
Pecksniff's Active
Penhaligon's Blenheim Bouquet*
Perry Ellis 360 Degrees Red
Pino Silvestre Modern Dandy
Ralph Lauren Big Pony 1, RL Chaps
Rasasi Chastity
Royal Barber Silver Razor
Royal Copenhagen 1775 Classic
Royall Lyme Bermuda Royall Lyme*
Shulton Old Spice Lime
Taylor of Old Bond Street No 74*
Tommy Bahama Set Sail St. Barts*
Tommy Hilfiger Citrus Brights, TH T
Truefitt & Hill Sandalwood, T&H West Indian Lime
Versace Baby Blue Jeans
Yardley Gold
Yves Rocher Antarctic, YR Bois de Cedre et Citron Vert, YR Comme Une Evidence Green
Zara Silver
Zirh

Limetta

Limetta (aka sweet lime, sweet lemon, sweet limetta, mousambi), considered to be a hybrid between bitter orange and citron, is also used in perfumery. It has a fine citrus scent reminiscent of lime but less acidic and slightly sweeter. One masculine fragrance with limetta is Sybarite Spicy Calabria.
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Finger Lime (C. australasica)

The finger lime (sometimes called caviar lime or caviar lemon) is a shrub or small tree of lowland tropical rainforest in the coastal border area of Queensland and New South Wales, Australia. Its oil is used in perfumery and has a fresh, sweet, clean, citrus fragrance with balsamic coumarin undertones. Masculine fragrances with finger lime include Jimmy Choo Urban Hero, Lacoste L.12.12 EdP Blanc, and Perry Ellis Bold Red.
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Kaffir Lime (c. hystrix)

The Kaffir lime or Makrut lime, including the leaves, is sometimes used in perfumery. Masculine compositions containing it include l'Bel 1200 Degrees C and Jequiti Azul.
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Mojito

Mojito is a fresh fantasy note reminiscent of the mojito drink (lime, mint, sometimes rum).
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Masculine fragrances said to have this note include:

Antonio Banderas Cocktail Seduction Blue
Calvin Klein CK One Shock Street Edition, CK Encounter Fresh
Caribbean Joe
Carolina Herrera 212 Men Pop!
David Beckham Beyond
Demeter Mojito (unisex)
Guerlain Homme
Masaki Matsuchima Mat;Stone
New Yorker Style Up
One of my favorite notes! Bohemian Lime IMO has one of the best lime notes and uses finger limes
 
It is real hard to find better educational material than one can find here.

Thank you so much for the hard work and sharing!
 
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