Jasmine aroma

Jasmonan. [Henkel/Emery/Cospha] Jasmine aroma chemical. 

Like many odors, that for coffee has many individual contributors. Nonetheless, we do not, indeed cannot, identify the individual compounds that contribute to the aroma. All we get is the smell of coffee. With a single odorant, say jasmine, many of us can identify it correctly. But if an aroma contains two components, only about one person in six can identify both correctly. And only about one person in 25 can unravel a mixture containing three components. Nobody gets it right if the aroma contains four or more components. Our brain basically integrates all the inputs and gives us a single sensation, not multiple, individually identifiable sensations. 

Beyond that, the sense of olfaction does not depend on the concentration of the odorant concentration invariance. If you are exposed to jasmine at very low concentration, it smells like jasmine if the concentration is significantly raised, it still smells like jasmine. Perhaps more to the point is the concentration invariance of complex aromas such as that of coffee. The brain forms a single perception from complex inputs, regardless of the intensity of the signal. Olfaction has this property in common with taste. 

Lmalool [78-70-6] - [PERFUMES] (Vol 18) - [TERPENOIDS] (Vol 23) -in anise star oil [OILS, ESSENTIAL] (Vol 17) -aroma chemical [PERFUMES] (Vol 18) -in Bergamot oil [OILS, ESSENTIAL] (Vol 17) -in caraway oil [OILS, ESSENTIAL] (Vol 17) -m Geranium Bourbon oil [OILS, ESSENTIAL] (Vol 17) -in jasmin oil [OILS, ESSENTIAL] (Vol 17) -in lavender [OILS, ESSENTIAL] (Vol 17) -in lavender [OILS, ESSENTIAL] (Vol 17) -in lime oil [OILS, ESSENTIAL] (Vol 17) -odor of [FLAVORCHARACTERIZATION] (Vol 11) -in oilbanum [OILS, ESSENTIAL] (Vol 17) -in orange oil [OILS, ESSENTIAL] (Vol 17) -m osmanthus flowers [OILS, ESSENTIAL] (Vol 17) -in otto of rose [OILS, ESSENTIAL] (Vol 17) -in sweet basil oil [OILS, ESSENTIAL] (Vol 17) -in wine [WINE] (Supplement)... 

Green tea is usually made from Camellia sinensis var. sinensis (small leaf type). In China, jasmine tea is made from common kamairi-cha (from var. sinensis) while var. assamica (large leaf type) is used for Indonesian jasmine tea. The Indonesian jasmine tea has a stronger roast aroma than Chinese jasmine tea (3). The var. assamica tea leaf also contains a much higher level of polyphenolic catechins than var. sinensis. 

The creation of Chanel No. 5 was based on the bold imaginative use of then available aroma chemicals in combination with fine natural products. Rose and jasmin absolutes were probably used at levels of around 4% or 5%, which would not have been unusual at the time when the perfume was created. In addition there would have been natural musk, ambergris, and civet. 

The most classical artificial substances used in perfumery are as follows (Figure 5). Hydroxycitronellal (99) was found to exhibit the odor of lily of the valley, the essential oil of which is not possible to prepare in the first place. Other classics include ct-amylcinnamaldehyde (100) and musk ketone (101), which were discovered to be good substitutes for jasmine and musk, respectively. Furthermore, perfume No. 5 (Chanel, launched 1921) contained 2-methylundecanal, 1 with so unique an aroma character that it established No. 5 as the pioneer of a new fragrance class — floral aldehydic. 

In this way, many other cannon and uncommon flowers such as jasmine, narcissus, osmanthus, honeysuckle, l acinth, lily-of-the-valley, lilac, and tuberose have been analyzed. In all cases, considerable differences have been observed in the aroma profiles of the living and picked flowers. In connection with the living flower analytical program, the concept was also extended to the flavor field, especially fruits. The fruits and flowers work has served as the basis of a recent report to the 10th International Congress of Essential Oils in Washington, D.C. in 1986. 

C11H12O2, Mr 176.21, bpi z kpa 139-140 °C, d22 1.0520, rag0 1.5420, is the only ester of cinnamic alcohol of any importance. fraras-Cinnamyl acetate occurs in cassia oil and is a colorless liquid with a sweet-flowery-fruity, slightly balsamic odor. It is a good fixative and is used in blossom compositions (e.g., lilac and jasmine) and for oriental notes. In aroma compositions, it is used for cinnamon-fruity effects. 

The methyl ester of jasmonic acid (methyl 3-oxo-2-(2 -pentenyl)-cyclopentaneacetate) is also known as both an active plant hormone and an important fragrance and flavor component with sweet-floral and jasmine-like aroma notes (13). Methyl jasmonate induces plant systems to provide defense from microbial infection, and is a secondary synthesis product of plants. Methyl jasmonate was also isolated from the Oriental fruit moth, Grapholitha molesta as a part of the male sex hormone (7,75). The authors demonstrated that the volatile form of jasmonic acid, methyl jasmonate, is a major signal molecule for inter- and intra species communications. Methyl jasmonate is expected to have... 

Products and Uses A colorless liquid with a floral aroma used in artificial jasmine, perfumes, soap perfume, lacquers, polishes, inks, and varnish remover. 

Products and Uses A jasmine-type odor for fruit, berry, beverage honey flavorings, desserts, candies, and bakery products used as a flavoring, aroma, and taste enhancer. 

The examples of the cis-trans-isomerizoXion are the photoreaction of a-ionone 1 and jasmone 2 as shown in Scheme 6. a-Ionone has a fresh violet-like odor and a warm-woody balsamic-floral odor of deep sweetness and moderate tenacity. It is used widely in all types of perfume compositions (Shibamoto and Mihara, 1983). cz5-a-Ionone is yielded from trans-a-ionone by photo irradiation (Buchi and Yang, 1955). Jasmone, which has a jasmine-like odor, is the principal aroma component in jasmine oil (Nofal et al. 1982 Toda et aL, 1983). On irradiation, jasmone gives the final products trans- and cis-2- 2 -ethylcyclopropyl)-3-methyl-2-cyclopenten-l-one (Tateba and Mihara, 1986). These two products are described as having a waxy, oily, and cz -jasmone-like odor for trans-form and a cz -jasmone-like odor with a mild, minty, and woody undertone for cz5--form. 

Heptanal, which can be produced by hydroformylation of 1-hexene (Table 6.1, entry 2), has a strong fruity odor and is widely used as an ingredient in the aroma industry. In dilution, it develops a sweet, fruity, nutty, fatty-cognac-like scent. Also its dimethyl acetal is employed, which confers the product a green, herbaceous, and somewhat nutty odor. It is occasionally added to soap perfumes. Aldol condensation with benzaldehyde gives a-hexyl cinnamaldehyde its odor is described as sweet and floral and reminiscent of jasmine. It is widely used in domestic fragrances [19]. 

Because many compoxmds containing benzene rings have pleasant aromas, benzene rings are also called aromatic rings, and compoxmds containing them are called aromatic compounds. For example, the pleasant smells of cinnamon, vanilla, and jasmine are all caused by aromatic compounds. 

Ethyl butyrate is responsible for the sweet aroma of pineapples. Other common esters include methyl butyrate, found in apples, and ethyl formate, an artificial rum flavor. Several perfumes use esters to impart a pleasant smell. For example, oil of jasmine contains benzyl acetate, a molecule found in the jasmine flower. 

In addition to the 5-lactones of structure (41), other lactonic aroma components with a saturated ring are known, the structure of which, however, is somewhat different from that of the n-series represented by (41). These are 6-hydroxy-5-hexanolide (42), identified in tomato (557), and three cyclic compounds carrying an unsaturated chain in position 5, viz. (Z)-7-decen-5-olide (jasmine lactone) (44) 712), identified in the flavor of black tea (50) together with methyl jasmonate (779). (Z)-9-dodecen-5-olide (45) and (Z)-9-tetradecen-5-olide (46), the latter two lactones having been isolated from butter flavor (50, 725). On the other hand, lactone (43) was isolated from milk where it is present in a quantity of 10 pg/kg (0.001 ppb) (247) this quantity, however, is probably much lower than the threshold value. 

Although the number of aroma compounds derived from acyclic carotenoids is much inferior to that of the mono- and bicyclic compounds, some of them can also be considered as breakdown products from genuine mono-, sesqui- and diterpenoids. The importance of the aliphatic isoprenoids (282) to (291) in the formation of total flavors of certain foodstuffs is not less than that of the cyclic compounds, the three methyl ketones (282), (287) and (290) which are related to the main tomato pigment lycopene were observed in tomato flavor (75). The hexahydro derivative (291) from coffee (595), jasmine oil (722) and green tea 438) is perceived as flowery and warm and can be considered as an oxidative biodegradation product of phytol and phyta-diene. 6-Methyl-3,5-heptadien-2-one (283), with a grassy and cinnamonlike aroma 438) [detected in tomato 668), the essential oil of Hama-metis leaves 383), Ceylon tea (722) and passion fruit (777)], and pseudo-ionone (288) [also isolated from passion fruit (777)] are believed to be formed from two different dehydrolycopenes. Compounds other than carotenoids, such as solanesol or squalene, can also be considered... 

Indole is a colorless sohd forming leaflet crystals, moderately soluble in water, of mp 52 °C and bp 253 °C. It occurs in coal tar and jasmine oil. Indole has an unpleasant fecal-like odor, but in high dilution has a pleasantly flowery aroma. It was found recently that indole is one of the compounds responsible for the smell of flowering rape fields. 

Jasmine Rice that possess a characteristic floral aroma and flavor once cooked. It contains low... 

On the other hand, perfumes, and also the pure fragrance chemicals that compose the perfume, can also be classified according to the note they provide, i.e. according to the fragrance type. So, one can find different types, like floral, which reminds one of scents similar to jasmine, rose, heliotrope, etc citrus, which are aromas reminiscent of lemon, orange, lime, grapefruit, etc. fruity, based on non-citrus fruity odours like peach. 

---