2734-47-6 Usage
Description
CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID METHYL ESTER, also known as Methyl all-cis-5,8,11,14,17-eicosapentaenoate, is a fatty acid methyl ester derived from Eicosapentaenoic acid (E477800). It is a highly unsaturated compound that is extracted from algae and is known for its practical applications in various industries.
Uses
Used in Agricultural Industry:
CIS-5,8,11,14,17-EICOSAPENTAENOIC ACID METHYL ESTER is used as a protective agent for stored grains against rice weevils. Its application reason is due to its ability to act as a deterrent for these pests, thus helping to preserve the quality and quantity of stored grains.
Check Digit Verification of cas no
The CAS Registry Mumber 2734-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2734-47:
(6*2)+(5*7)+(4*3)+(3*4)+(2*4)+(1*7)=86
86 % 10 = 6
So 2734-47-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H32O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h4-5,7-8,10-11,13-14,16-17H,3,6,9,12,15,18-20H2,1-2H3/b5-4-,8-7-,11-10-,14-13-,17-16-
2734-47-6Relevant articles and documents
DIRECT METHOD AND REAGENT KITS FOR FATTY ACID ESTER SYNTHESIS
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Page/Page column 18; 21-22; 29, (2008/12/07)
Provided are efficient, cost-effective and water tolerant methods (e.g., single-vial methods) for preparing fatty acid esters from organic matter, comprising: obtaining organic matter comprising at least one fat substituent, contacting the organic matter in a reaction mixture with a basic solution under conditions suitable to provide for hydrolytic release of monomeric fatty acids from the at least one fat substituent to provide a base-treated reaction mixture, and esterifying the monomeric fatty acids of the base-treated reaction mixture by acidification of the reaction mixture and treating in the presence of an organic alcohol to provide fatty acid esters. The methods optionally further comprise, prior to esterifying, neutralizing the base-treated reaction mixture to provide for neutralized fatty acids, separating the neutralized fatty acids from the neutralized reaction mixture, and dissolving the separated fatty acids in the esterification reaction mixture. Also provided are related methods and kits for fat analysis.
