1072-39-5 Usage
Description
Erucic acid, a monounsaturated omega-9 fatty acid, is predominantly found in certain plant sources like rapeseed and mustard seed, and in trace amounts in some animal fats, especially marine animal fats. Despite its potential health risks linked to heart, liver, and nervous system issues in animal studies, it is regulated in food products but finds utility in industrial applications.
Uses
Used in Industrial Applications:
Erucic acid is used as a raw material for the production of various industrial products due to its unique properties.
Used in Lubricant Production:
Erucic acid is used as a base oil in the formulation of lubricants for its ability to provide high viscosity and film strength, which are essential for reducing friction and wear in mechanical applications.
Used in Plastics Industry:
Erucic acid is utilized as a monomer in the synthesis of specific types of plastics, contributing to the development of materials with tailored properties for various uses.
Used in Cosmetics:
Erucic acid is employed in the cosmetics industry, where it serves as an ingredient in personal care products, potentially offering moisturizing and conditioning effects on the skin and hair.
Check Digit Verification of cas no
The CAS Registry Mumber 1072-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1072-39:
(6*1)+(5*0)+(4*7)+(3*2)+(2*3)+(1*9)=55
55 % 10 = 5
So 1072-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(23)24/h9-10H,2-8,11-21H2,1H3,(H,23,24)/b10-9-
1072-39-5Relevant articles and documents
A new and highly effective organometallic approach to 1,2-dehalogenations and related reactions
Azzena, Ugo,Pittalis, Mario,Dettori, Giovanna,Pisano, Luisa,Azara, Emanuela
, p. 3892 - 3900 (2008/03/12)
We investigated the reductive elimination of several functionalized and non-functionalized vic-dibromides with 1,2-diphenyl-, 1,1,2,2-tetraphenyl- and 1-phenyl-2-(2-pyridyl)-1,2-disodioethane. The reaction, involving some of the less expensive organic and inorganic reagents, proceeds under mild conditions, and is tolerant of a variety of functional groups. Extension of this procedure to similar 1,2-disubstituted compounds was also investigated. Reductive eliminations run on stereochemical probe compounds strongly suggest that this reaction proceeds via a "single electron" reductive elimination reaction pathway.
