106554-63-6 Usage
Description
(Z)-methyl hexadec-6-enoate, also known as palmitoleic acid methyl ester, is a naturally occurring chemical compound that is widely found in various sources such as vegetable oils, fish oils, and animal fats. It is an ester of palmitoleic acid, which is a monounsaturated omega-7 fatty acid. (Z)-methyl hexadec-6-enoate is known for its distinctive fruity and floral aroma, as well as its potential health benefits, including anti-inflammatory and antimicrobial properties. Research is ongoing to explore its therapeutic potential in the treatment of metabolic and inflammatory diseases.
Uses
Used in the Fragrance and Flavor Industry:
(Z)-methyl hexadec-6-enoate is used as a flavoring agent for its fruity and floral aroma, enhancing the sensory experience of various food products.
Used in the Pharmaceutical Industry:
(Z)-methyl hexadec-6-enoate is used as an active ingredient for its anti-inflammatory and antimicrobial properties, potentially contributing to the development of treatments for metabolic and inflammatory diseases.
Used in the Cosmetics and Personal Care Industry:
(Z)-methyl hexadec-6-enoate is used as a moisturizing and skin-nourishing agent in the production of cosmetics and personal care products, improving the skin's health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 106554-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106554-63:
(8*1)+(7*0)+(6*6)+(5*5)+(4*5)+(3*4)+(2*6)+(1*3)=116
116 % 10 = 6
So 106554-63-6 is a valid CAS Registry Number.
106554-63-6Relevant articles and documents
Substrate specificity of regiospecific desaturation of aliphatic compounds by a mutant Rhodococcus strain.
Koike,Takaiwa,Kimura,Inoue,Ito
, p. 1064 - 1066 (2000)
Substrate specificity of cis-desaturation of alipahtic compounds by resting cells of a mutant, Rhodococcus sp. strain KSM-MT66, was examined. Among substrates tested, the rhodococcal cells were able to convert n-alkanes (C13-C19), 1-chloroalkanes (C16 and C18), ethyl fatty acids (C14-C17) and alkyl (C1-C4) esters of palmitic acid to their corresponding unsaturated products of cis configuration. The products from n-alkanes and 1-chloroalkanes had a double bond mainly at the 9th carbon from their terminal methyl groups, and the products from acyl fatty acids had a double bond mainly at the 6th carbon from their carbonyl carbons.
