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13487-42-8

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13487-42-8 Usage

Description

CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER, also known as cis-7,10,13,16-docosatetraenoic acid methyl ester, is a naturally occurring fatty acid ester derived from docosahexaenoic acid (DHA). It is characterized by its unique structure, which includes multiple double bonds and a methyl ester group. CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER is known for its potential health benefits and applications in various industries.

Uses

Used in the Pharmaceutical Industry:
CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER is used as a pharmaceutical compound for its potential health benefits. It is believed to have anti-inflammatory, anti-atherogenic, and neuroprotective properties, making it a promising candidate for the development of drugs targeting various health conditions.
Used in the Food Industry:
In the food industry, CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER is used as a nutritional supplement due to its omega-3 fatty acid content. It is often added to fortified foods and dietary supplements to promote heart and brain health.
Used in the Cosmetics Industry:
CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER is used as an ingredient in cosmetics for its moisturizing and anti-aging properties. It is believed to help maintain skin elasticity and reduce the appearance of fine lines and wrinkles.
Used in Oregano Essential Oil Production:
CIS-7,10,13,16,19-DOCOSA-TETRAENOIC ACID METHYL ESTER is used in oregano essential oil as an inhibitor of higher fatty acid oxidation. This application helps to preserve the quality and aroma of the essential oil, making it more stable and longer-lasting.

Check Digit Verification of cas no

The CAS Registry Mumber 13487-42-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13487-42:
(7*1)+(6*3)+(5*4)+(4*8)+(3*7)+(2*4)+(1*2)=108
108 % 10 = 8
So 13487-42-8 is a valid CAS Registry Number.
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-

13487-42-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl cis-7,10,13,16-Docosatetraenoate

1.2 Other means of identification

Product number -
Other names cis-7,10,13,16-Docosatetraenoic acid methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13487-42-8 SDS

13487-42-8Downstream Products

13487-42-8Relevant 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.

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