13487-42-8

Basic information

• Product Name: CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER
• Synonyms: CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER;cis-7,10,13,16-docosatetraenoic acid*methyl ester;Methyl cis-7,10,13,16-Docosatetraenoate;Methyl 7,10,13,16-docosatetraenoate (all-cis);cis-7,10,13,16-Docosatetraenoic ac;(7Z,10Z,13Z,16Z)-7,10,13,16-Docosatetraenoic acid methyl ester;Methyl 7Z,10Z,13Z,16Z-docosatetraenoate;7,10,13,16-Docosatetraenoicacid, methyl ester, (7Z,10Z,13Z,16Z)-
• CAS NO: 13487-42-8
• Molecular Formula: C₂₃H₃₈O₂
• Molecular Weight: 346.55
• Product Categories: Esters;Methyl Esters;Unsaturated fatty acids and derivatives
• Mol File: 13487-42-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 432.1°C at 760 mmHg
• Flash Point: 99.2°C
• Appearance: /
• Density: 0.897g/cm³
• Vapor Pressure: 1.14E-07mmHg at 25°C
• Refractive Index: 1.4821 (589.3 nm 25℃)
• Storage Temp.: −20°C
• CAS DataBase Reference: CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER(13487-42-8)
• EPA Substance Registry System: CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER(13487-42-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 13487-42-8(Hazardous Substances Data)

Usage

Uses

cis-7,10,13,16-Docosatetraenoic Acid Methyl Ester is used in oregano essential oil as an inhibitor of higher fatty acid oxidation.

InChI:InChI=1/C23H38O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25-2/h7-8,10-11,13-14,16-17H,3-6,9,12,15,18-22H2,1-2H3/b8-7-,11-10-,14-13-,17-16-

Upstream product

• 186581-53-3 diazomethane 
• 10434-01-2 Docosa-7,10,13,16-tetrain-1-saeure 
• 67-56-1 methanol 
• 124-41-4 sodium methylate 
• 34498-19-6 1-iodo-undeca-2,5-diyne 
• 10297-08-2 Undecan-7,10-diin-1-saeure 
• 34498-26-5 1-bromo-2,5,8-tetradecatriyne 
• 10297-09-3 oct-7-ynoic acid 

Relevant articles and documents

DIRECT METHOD AND REAGENT KITS FOR FATTY ACID ESTER SYNTHESIS

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.