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65119-95-1

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65119-95-1 Usage

General Description

22-Tricosenoic acid is a long-chain unsaturated fatty acid that is commonly found in plant and animal lipids. It is classified as a monounsaturated fatty acid due to its single double bond located 22 carbons from the carboxylic acid end. This fatty acid is primarily used in the production of cosmetics and skincare products due to its emollient and moisturizing properties. It is also used in the manufacturing of soaps and detergents, as well as in the food industry as a flavoring agent and a source of dietary fat. Additionally, 22-Tricosenoic acid has been studied for its potential health benefits, including its role in reducing inflammation and promoting heart health.

Check Digit Verification of cas no

The CAS Registry Mumber 65119-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65119-95:
(7*6)+(6*5)+(5*1)+(4*1)+(3*9)+(2*9)+(1*5)=131
131 % 10 = 1
So 65119-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H44O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23(24)25/h2H,1,3-22H2,(H,24,25)

65119-95-1SDS

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 22-Tricosenoic Acid

1.2 Other means of identification

Product number -
Other names tricos-22-enoic acid

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:65119-95-1 SDS

65119-95-1Downstream Products

65119-95-1Relevant articles and documents

Synthesis of ω-Unsaturated Acids

Mirviss, Stanley B.

, p. 1948 - 1951 (2007/10/02)

A short, high-yield method for the synthesis of ω-unsaturated acids have been developed that precludes any double-bond migration or hydrogenation.Key is the coupling reaction between Grignards of ω-unsaturated alkyl halides and the bromomagnesium salt of ω-bromo fatty acids.The reaction has been successfully extended to ω-bromo nitriles.The use of ω-chloro acids or α-bromo acids gives lower yields of heterocoupling products and substantial homocoupling.A catalyst study shows Li2CuCl4 to yield the most heterocoupling of several catalysts tried for the chloro acids, and Ni(II) or Cu(I) are best for the α-bromo acids.

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