57491-35-7 Usage
Description
(3Z,13E)-octadeca-3,13-dienyl acetate, also known as Linoleyl acetate, is a long-chain fatty acid derivative that belongs to the class of organic compounds. It is a colorless to pale yellow liquid with a fruity, floral scent and is commonly found in various fruits and flowers. This chemical is known for its pleasant aroma and is often used in the production of perfumes, flavorings, and cosmetics. Moreover, it also serves as a flavoring agent in the food industry. Studies have revealed that (3Z,13E)-octadeca-3,13-dienyl acetate possesses anti-inflammatory and antioxidant properties, making it potentially beneficial for skincare and other therapeutic applications.
Uses
Used in Perfume Industry:
(3Z,13E)-octadeca-3,13-dienyl acetate is used as a fragrance ingredient for its fruity, floral scent, contributing to the overall aroma of perfumes.
Used in Flavoring Industry:
(3Z,13E)-octadeca-3,13-dienyl acetate is used as a flavoring agent in the food industry to enhance the taste and aroma of various food products.
Used in Cosmetics Industry:
(3Z,13E)-octadeca-3,13-dienyl acetate is used as an ingredient in cosmetics due to its pleasant aroma and potential anti-inflammatory and antioxidant properties, making it beneficial for skincare applications.
Used in Therapeutic Applications:
(3Z,13E)-octadeca-3,13-dienyl acetate is used for its anti-inflammatory and antioxidant properties, which may offer potential benefits in various therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 57491-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,9 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57491-35:
(7*5)+(6*7)+(5*4)+(4*9)+(3*1)+(2*3)+(1*5)=147
147 % 10 = 7
So 57491-35-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-20(2)21/h6-7,16-17H,3-5,8-15,18-19H2,1-2H3/b7-6+,17-16-
57491-35-7Relevant articles and documents
Synthesis and characterization of 3,13- and 2,13-octadecadienyl compounds for identification of the sex pheromone secreted by a clearwing moth, Nokona pernix
Naka, Hideshi,Nakazawa, Tomotake,Sugie, Mieko,Yamamoto, Masanobu,Horie, Yoshiteru,Wakasugi, Ryohei,Arita, Yutaka,Sugie, Hajime,Tsuchida, Koji,Ando, Tetsu
, p. 508 - 516 (2008/02/10)
Several geometrical isomers of 3,13- and 2,13-octadecadien-1-ols and their acetates were synthesized starting from 1,8-octanediol or 1,9-nonanediol utilizing acetylene coupling reactions. In addition to commercially available compounds, all geometrical isomers of each dienyl compound were analyzed by NMR and GC-MS to accumulate chemical data for studies of sex pheromones secreted from clearwing moths classified into the family Sesiidae of Lepidoptera. Although acetoxy derivatives of the 3,13- and 2,13-dienes showed almost the same mass spectra, the alcohols were distinguished by comparing the relative intensities of [M - 18]+ at m/z 248, indicating direct differentiation of the two positional isomers without derivatization. Furthermore, each geometrical isomer eluted from a high-polar GC column with a different retention time. Base on these data, a pheromone gland extract of a sesiid moth, Nokona pernix, was analyzed by GC-EAD and GC-MS, and two EAG-active components were identified, viz., the (3E,13Z)- and (3Z,13Z)-isomers of 3,13-octadecadien-1-ol in a ratio of 9:1. In the field, the synthetic compounds mixed in 9:1 ratio attracted N. pernix males well, while a single component scarcely attracted the males. The number of attracted males peaked in the middle of June, and a small second peak was observed in August.
