Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Fruity fragrances

Dihydrojasmone is used in perfumery in jasmin bases and, more generally, in blossomy and fruity fragrances. [Pg.85]

Prend. [BASF AG] 3-Methyl-2-butene-l-ol fresh, herbal, green, fruity fragrance and flavoring. [Pg.294]

Features Ethereal, fruity fragrance and flavor, rumlike on dilution... [Pg.1739]

Features Floral-fruity fragrance with suggestion of wood... [Pg.2628]

Methyl butanoate, an oily substance with a strong fruity fragrance can be made by reacting butanoic acid with methanol according to the following equation ... [Pg.832]

PRACTICE EXAMPLE A Compound A with the formula CsHgO is soluble in water and reacts with sodium metal, producing bubbles of gas. When compound A is treated with chromic acid (a mixture of Na2Cr207 and H2SO4), compound B is formed. Compound B dissolves readily in Na2C03(aq) and reacts with ethanol, yielding compound C which has a fruity fragrance. Identify compounds A, B, and C. [Pg.1258]

The odors of single chemical compounds are extremely difficult to describe unequivocally. The odors of complex mixtures are often impossible to describe unless one of the components is so characteristic that it largely determines the odor or flavor of the composition. Although an objective classification is not possible, an odor can be described by adjectives such as flowery, fruity, woody, or hay-like, which relate the fragrances to natural or other known products with similar odors. [Pg.6]

Straight-chain, saturated aliphatic acids are found in many essential oils and foods. These acids contribute to aromas, but are not important as fragrance substances. In flavor compositions, aliphatic acids up to Cio are used to accentuate certain aroma characteristics (C3-C8 for fruity notes C4, C6-C12 for cheese flavors). However, straight-chain and some branched-chain aliphatic acids are of... [Pg.17]

In perfumery, acetates are the most important aliphatic esters formates do not keep well. Animal and fatty notes become more pronounced in esters of higher fatty acids. Acetates of alcohols up to C(, are used principally for fruity notes, whereas the acetates of Cg, Cio, and C12 alcohols are employed for blossom fragrances and for flower notes in general. Lauryl acetate in particular is also used for conifer notes. [Pg.18]

It is used in fragrances to enhance fruity notes and in strawberry flavors. [Pg.18]

Uses. Linalool is used frequently in perfumery for fruity notes and for many flowery fragrance compositions (lily of the valley, lavender, and neroli). Because of its relatively high volatility, it imparts naturalness to top notes. Since linalool is stable in alkali, it can be used in soaps and detergents. Linalyl esters can be prepared from linalool. Most of the manufactured linalool is used in the production of vitamin E. [Pg.30]

C12H22O2, Mr 198.30, Z PlOl.SkPa 240 °C, d 0.8901, Wp 1.4515, occurs in many essential oils either as one of its optical isomers or as the racemate. The odor of racemic citronellyl acetate differs little from that of the optical isomers. ( )-Citronellyl acetate is a liquid with a fresh-fruity rose odor. It is often used as a fragrance, for example, for rose, lavender, and geranium notes as well as for eau de cologne with citrus nuances. Since it is relatively stable to alkali, it can be used in soaps and detergents. Citrus flavors acquire speciflc character through the addition of citronellyl acetate it is also used to round off other fruit flavors. [Pg.46]

C13H22O2, Mr 210.32 is a mixture of isomers, bpo kPa 102 °C, ng 1.4626, a colorless to pale yellow liquid with rosy, spicy, fruity, and woody odor. For its preparation 3,6-dimethyl-6-hepten-2-one and 7-methyl-6-octen-3-one are treated with ethyl diethylphosphoryl acetate to give a mixture of octadienoic acid esters. Cyclization with sulfuric/formic acid yields the title compounds as a mixture with isomers [134]. With its complex odor picture it is used in fine fragrances for shading. [Pg.93]

It is prepared by treating ethyl cinnamate with peracetic acid [212] or by condensation of benzaldehyde with ethyl chloroacetate (in the above Darzens reaction, R = H). The glycidate is used as a long-lasting fragrance material for creating harmonic, fruity notes in household and fine fragrances. [Pg.161]

Blackcurrant absolute is used in fine fragrances and in fruity food flavors. [Pg.178]

It is used in accentuated flowery fragrances and in aroma compositions to achieve fruity effects. FCT 1982 (20) 829 [8016-84-0], [91770-75-1]. [Pg.220]

Esters are widespread in fruits and especially those with a relatively low molecular weight usually impart a characteristic fruity note to many foods, e.g. fermented beverages [49]. From the industrial viewpoint, esterases and lipases play an important role in synthetic chemistry, especially for stereoselective ester formations and kinetic resolutions of racemic alcohols [78]. These enzymes are very often easily available as cheap bulk reagents and usually remain active in organic reaction media. Therefore they are the preferred biocatalysts for the production of natural flavour esters, e.g. from short-chain aliphatic and terpenyl alcohols [7, 8], but also to provide enantiopure novel flavour and fragrance compounds for analytical and sensory evaluation purposes [12]. Enantioselectivity is an impor-... [Pg.527]

Natural esters are widely used by the aroma and fragrance industries because of their fruity or floral taste/odor. Many of them are alkyl esters of formic, acetic, propionic, and butyric acids. The development of an efficient biotechnological process, compatible with the natural label for the products but offering costs comparable to the costs of chemical processes, has been achieved, representing the first application of gas/solid technology on an industrial scale [51]. [Pg.272]


See other pages where Fruity fragrances is mentioned: [Pg.73]    [Pg.152]    [Pg.93]    [Pg.40]    [Pg.78]    [Pg.162]    [Pg.40]    [Pg.294]    [Pg.2186]    [Pg.2606]    [Pg.2638]    [Pg.408]    [Pg.73]    [Pg.152]    [Pg.93]    [Pg.40]    [Pg.78]    [Pg.162]    [Pg.40]    [Pg.294]    [Pg.2186]    [Pg.2606]    [Pg.2638]    [Pg.408]    [Pg.2]    [Pg.18]    [Pg.22]    [Pg.22]    [Pg.23]    [Pg.44]    [Pg.44]    [Pg.46]    [Pg.92]    [Pg.93]    [Pg.95]    [Pg.116]    [Pg.117]    [Pg.128]    [Pg.134]    [Pg.15]    [Pg.498]    [Pg.305]   
See also in sourсe #XX -- [ Pg.126 ]




SEARCH



Fruity

© 2024 chempedia.info