41935-39-1 Usage
General Description
Bis(2-phenoxyethyl) peroxydicarbonate is an organic chemical compound that is used as a radical initiator in the emulsion polymerization of various monomers. It is a colorless to pale yellow liquid with a characteristic odor, and it is highly soluble in organic solvents such as acetone, toluene, and ethyl acetate. This chemical is a strong oxidizing agent and can decompose violently at temperatures above 70°C, so it should be handled with extreme care. It is commonly used in the production of polymers, resins, and adhesives due to its ability to effectively initiate the polymerization process. Additionally, it is also used in the synthesis of specialty chemicals and as a crosslinking agent in the production of elastomers.
Check Digit Verification of cas no
The CAS Registry Mumber 41935-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41935-39:
(7*4)+(6*1)+(5*9)+(4*3)+(3*5)+(2*3)+(1*9)=121
121 % 10 = 1
So 41935-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O8/c19-17(23-13-11-21-15-7-3-1-4-8-15)25-26-18(20)24-14-12-22-16-9-5-2-6-10-16/h1-10H,11-14H2
41935-39-1Relevant articles and documents
Synthesis of peroxydicarbonates containing alkyl-aromatic fragments and investigation of their properties
Etlis, I.V.,Fomin, V.A.,Nozrina, F.D.
, p. 2010 - 2015 (2007/10/02)
The reaction of alkyl-substituted benzyl- and naphthylmethyl-chloroformates with Na2O2 or cyclohexyloxyperoxycarbonic acid at 0-5 deg C leads to symmetric and asymmetric peroxydicarbonates.Investigation of the thermolysis kinetics of the peroxides at 50-70 deg C showed that the structure of the organic fragment influences the rate of homolysis of the O-O bond to a great extent.This is characteristic in particular for compounds containing substituents in the ortho-position, where the presence of methyl radicals leads to a decrease in the contribution of the induced dissociation to the overall rate of homolysis of the peroxides obtained
