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(9E)-octadec-9-en-1-yl acetate, also known as oleyl acetate, is a long-chain fatty acid derivative commonly found in plants and fruits. It is an ester formed from octadec-9-enoic acid (oleic acid) and acetic acid, and is known for its pleasant and sweet aroma.

22147-38-2

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22147-38-2 Usage

Uses

Used in Flavor and Fragrance Industry:
(9E)-octadec-9-en-1-yl acetate is used as a flavoring agent for its fruity and floral notes, contributing to the pleasant and sweet aroma of fruits such as apples and bananas.
Used in Pheromone Production:
In the field of entomology, (9E)-octadec-9-en-1-yl acetate is used as a component of pheromones in certain insect species, playing a crucial role in their communication and mating behavior.
Used in Food Industry:
(9E)-octadec-9-en-1-yl acetate is utilized as an additive in the food industry due to its appealing flavor and aroma, enhancing the sensory experience of various food products.
Used in Cosmetic Products:
This chemical is also considered safe for use in cosmetic products, where it may be employed for its pleasant scent and potential emollient properties.
Safety:
(9E)-octadec-9-en-1-yl acetate has been recognized as safe (GRAS) by the Food and Drug Administration for its use in the food and cosmetic industries.

Check Digit Verification of cas no

The CAS Registry Mumber 22147-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,4 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22147-38:
(7*2)+(6*2)+(5*1)+(4*4)+(3*7)+(2*3)+(1*8)=82
82 % 10 = 2
So 22147-38-2 is a valid CAS Registry Number.

22147-38-2Relevant academic research and scientific papers

Acetylation and formylation of alcohols with triphenylphosphine and carbon tetrabromide in ethyl acetate or ethyl formate

Hagiwara, Hisahiro,Morohashi, Kimie,Sakai, Hitoshi,Suzuki, Toshio,Ando, Masayoshi

, p. 5845 - 5852 (1998)

Alcohols were acetylated or formylated with triphenylphosphine and carbon tetrabromide in ethyl acetate or ethyl (or methyl) formate at room temperature. THP or TBDMS ether of primary alcohol got converted into formate or acetate under the experimental conditions employed in one pot operation.

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