By Kurt Bauer, Dorothea Garbe, Horst Surburg
Get an outstanding begin in taste and body spray chemistry! This publication offers a survey of these common and artificial body spray and style fabrics that are remoted and produced commercially on a comparatively huge scale due to their organoleptic features. It presents info on their houses, tools hired of their manufacture, and their components of software. '...The very good and concise creation to this specified is through broad details on approximately 500 of the main used perfume and taste compounds. Names, molecular formulation, actual info, smell and style descriptions, makes use of, and a couple of approaches for the bigger quantity chemical substances are all integrated. Successive chapters take care of crucial oils, animal secretions, qc, toxicology and literature. The formulation, identify and CAS registry quantity index is a useful and well timed addition.' Parfumer and Flavorist '...This booklet offers loads of precious info in a single position, and it's a particularly sturdy source for someone simply getting into the flavour and perfume industry.' magazine of Medicinal Chemistry 'You'll locate a lot info during this publication now not present in different works.' Foster's Herb company Bulletin 'Particularly helpful for usual product chemists, these within the product improvement and the curious.' Herbalgram
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Additional resources for Common Fragrance and Flavor Materials: Preparation, Properties and Uses, Third Edition
827. 4731, is an isomer of geraniol and linalool. It has been identified in Chinese lavender oil  and some medicinal plants. It is a colorless liquid with a fresh-flowery, slightly limelike odor. , antioxidants such as ionol). Myrcene Myrcenol Myrcenol can be prepared by treating niyrcene with diethylamine to give a mixture of geranyl- and neryldiethylamine. These compounds are hydrated with a dilute acid to the corresponding hydroxydiethylamines. Deamination to myrcenol is effected by using a palladium-phosphine-cation complex as a catalyst .
Citronellal is used to a limited extent for perfuming soaps and detergents. Its main use is as a starting material for the production of isopulegol, citronellol, and hydroxydihydroci tronellal. FCT 1975 (13) p. 55. 4488, has been reported to occur in essential oils . It is a colorless, slightly viscous liquid with a flowery odor reminiscent of linden blossom and lily of the valley. Commercially available ‘hydroxycitronellal’ is either optically active or racemic, depending on the starting material used.
It is not known to have been found in nature. 3,7-Dimethyl-7-methoxyoctan-2-ol is prepared by hydrochlorination of dihydromyrcene, methoxylation of the resulting 2-chloro-2,6-dimethyl-7-octene and epoxidation. The alcohol is obtained by hydrogenation of the epoxide in the presence of Raney nickel and triethylamine . It is used in perfumery as a top note in high quality sandalwood compositions for cosmetics, toiletries, and soaps. Trade Name. 4890, is a component of many blossom oils. It is a colorless liquid with a linden blossom odor, which becomes more intense when evaporated, possibly due to oxidation.