1932-84-9 Usage
Description
Dibenzyl azelate is an organic chemical compound that belongs to the ester class. It consists of two benzyl groups attached to the azelate (nonanedioate) functional group, which contributes to its unique properties and applications.
Uses
Used in Plasticizer Industry:
Dibenzyl azelate is used as a plasticizer for enhancing the flexibility, durability, and processing characteristics of various polymers, particularly in the manufacturing of PVC products.
Used in Adhesives, Sealants, and Coatings Industry:
Dibenzyl azelate is used as a component in the formulation of adhesives, sealants, and coatings to improve their performance and properties.
Used in Pharmaceutical Industry:
Dibenzyl azelate may have potential applications in the pharmaceutical industry, although specific uses are not detailed in the provided materials.
Used in Cosmetic Industry:
Dibenzyl azelate may also have potential applications in the cosmetic industry, although specific uses are not detailed in the provided materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1932-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1932-84:
(6*1)+(5*9)+(4*3)+(3*2)+(2*8)+(1*4)=89
89 % 10 = 9
So 1932-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H28O4/c24-22(26-18-20-12-6-4-7-13-20)16-10-2-1-3-11-17-23(25)27-19-21-14-8-5-9-15-21/h4-9,12-15H,1-3,10-11,16-19H2
1932-84-9Relevant articles and documents
Esterification of dicarboxylic acids with benzyl alcohol under the action of the microwave radiation
Aver'yanov,Batrakova,Samuilov,Spiridonova,Kochnev,Galibeev,Gnezdilov
experimental part, p. 1920 - 1923 (2009/02/08)
Reaction of dicarboxylic acid with benzyl alcohol under the microwave irradiation proceeds faster as compared to the thermal conditions. The main reaction products are alkyl dicarboxylates, and the monoester and dibenzyl ether are formed as the side products. A proposal about the nature of the nonthermal effect in the reactions stimulated by the microwave irradiation is considered.
