76649-25-7 Usage
Description
TRANS,CIS-3,6-NONADIEN-1-OL is an organic compound with a molecular formula of C9H14O. It is a colorless to pale yellow liquid with a strong, green, and cucumber-like odor. It is commonly found in various fruits and plants, particularly in melon, cucumber, and wax jambu (Syzygium samarangense Merr.).
Uses
Used in Flavor and Fragrance Industry:
TRANS,CIS-3,6-NONADIEN-1-OL is used as a flavoring agent for its heavy, waxy, fresh vegetative green cucumber and melon taste, with a fatty mouthfeel. It is added to various food products to enhance their flavor and aroma.
Used in Aromatherapy:
TRANS,CIS-3,6-NONADIEN-1-OL is used as an aromatherapy ingredient for its pleasant, sweet green, vegetative cucumber, melon, and honeydew aroma with waxy and oily nuances. It is believed to have calming and soothing effects on the mind and body.
Used in Perfumery:
TRANS,CIS-3,6-NONADIEN-1-OL is used as a fragrance ingredient in the perfumery industry due to its strong, green, and cucumber-like odor. It is used to create fresh and natural scents in various perfumes and colognes.
Used in Cosmetics:
TRANS,CIS-3,6-NONADIEN-1-OL is used as a fragrance ingredient in the cosmetics industry to add a pleasant and natural scent to various cosmetic products such as lotions, creams, and shampoos.
Used in the Food Industry:
TRANS,CIS-3,6-NONADIEN-1-OL is used as a flavoring agent in the food industry to enhance the taste and aroma of various food products, particularly those with a cucumber or melon flavor profile.
Check Digit Verification of cas no
The CAS Registry Mumber 76649-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,4 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76649-25:
(7*7)+(6*6)+(5*6)+(4*4)+(3*9)+(2*2)+(1*5)=167
167 % 10 = 7
So 76649-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-2-3-4-5-6-7-8-9-10/h3-4,6-7,10H,2,5,8-9H2,1H3/b4-3+,7-6+
76649-25-7Relevant articles and documents
Total syntheses and in vivo quantitation of novel neurofuran and dihomo-isofuran derived from docosahexaenoic acid and adrenic acid
De La Torre, Aurlien,Lee, Yiu Yiu,Mazzoni, Attilio,Guy, Alexandre,Bultel-Ponc, Valrie,Durand, Thierry,Oger, Camille,Lee, Jetty Chung-Yung,Galano, Jean-Marie
supporting information, p. 2442 - 2446 (2015/01/30)
Neurofurans (NeuroFs) and dihomo-isofurans (dihomo-IsoFs) are produced in vivo by non-enzymatic free-radical pathways from docosahexaenoic and adrenic acids, respectively. As these metabolites are produced in minute amounts, their analyses in biological samples remain challenging. Syntheses of neurofuran and dihomo-isofurans described are based on a pivotal strategy, thanks to an enantiomerically enriched intermediate, which allowed, for the first time, access to both families: the alkenyl and enediol. Owing to this formation, quantitation of specific NeuroF and dihomo-IsoFs in biological samples was attainable.
