37910-77-3 Usage
Description
Erucic Acid Ethyl Ester, also known as E649900, is a long-chain fatty acid ethyl ester derived from the formal condensation of the carboxy group of (13Z)-docosenoic acid with the hydroxy group of ethanol. It is a long-chain alcohol that acts as an inhibitor of fatty acid oxidation in the heart and is primarily found in rapeseed plant oil extracts and canola oil.
Uses
Used in Pharmaceutical Industry:
Erucic Acid Ethyl Ester is used as a therapeutic agent for treating conditions related to fatty acid oxidation in the heart. Its ability to inhibit fatty acid oxidation makes it a potential candidate for the development of drugs targeting heart-related disorders.
Used in Food Industry:
Erucic Acid Ethyl Ester is used as a component in the production of canola oil and rapeseed plant oil extracts. These oils are widely used in the food industry for cooking and as ingredients in various food products due to their nutritional benefits and desirable fatty acid profile.
Used in Cosmetics Industry:
Erucic Acid Ethyl Ester can be used as an ingredient in the formulation of cosmetics and personal care products. Its long-chain structure and fatty acid properties make it suitable for use in creams, lotions, and other skincare products to provide moisturization and improve skin health.
Used in Biodiesel Production:
Erucic Acid Ethyl Ester can be utilized as a component in the production of biodiesel. Its long-chain structure and compatibility with other fatty acid esters make it a valuable contributor to the development of sustainable and eco-friendly fuel sources.
Check Digit Verification of cas no
The CAS Registry Mumber 37910-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37910-77:
(7*3)+(6*7)+(5*9)+(4*1)+(3*0)+(2*7)+(1*7)=133
133 % 10 = 3
So 37910-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H46O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24(25)26-4-2/h11-12H,3-10,13-23H2,1-2H3/b12-11-
37910-77-3Relevant articles and documents
Preparation method of nervonic acid and nervonic acid
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Paragraph 0049-0051; 0056, (2020/07/27)
The invention discloses a preparation method of nervonic acid and nervonic acid. The preparation method comprises the following steps: preparing a Grignard reagent from 1-bromo-cis-13-docosaene, and carrying out an epoxy ring-opening reaction on the Grignard reagent, cuprous iodide and ethylene oxide to synthesize 1-hydroxy-cis-15-tetracosaene; and preparing nervonic acid by carrying out oxidationreaction on 1-hydroxy-cis-15-tetracosaene, iodobenzene acetate and TEMPO. By means of chemical synthesis, erucic acid is used as a raw material, and synthesis of nervonic acid is completed through esterification, reduction, bromination, Grignard reaction and oxidation. The method for synthesizing nervonic acid has the advantages of cheap and accessible raw materials, high yield, high product purity and the like, and is easy to operate.
