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Didodecyl peroxide, also known as di(C12) peroxide or bis(didodecyl) peroxide, is an organic compound with the chemical formula C24H50O2. It is a colorless, waxy solid that is widely used as a cross-linking agent in the polymer industry, particularly in the production of polyethylene and other plastics. Didodecyl peroxide is also employed as a curing agent for elastomers, a bleaching agent in the paper industry, and a catalyst in various chemical reactions. Due to its reactive nature, it is essential to handle didodecyl peroxide with caution, as it can decompose upon exposure to heat or light, releasing oxygen and forming potentially hazardous byproducts.

2895-03-6

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2895-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2895-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2895-03:
(6*2)+(5*8)+(4*9)+(3*5)+(2*0)+(1*3)=106
106 % 10 = 6
So 2895-03-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H50O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3

2895-03-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-dodecylperoxydodecane

1.2 Other means of identification

Product number -
Other names Didodecyl peroxide

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:2895-03-6 SDS

2895-03-6Upstream product

2895-03-6Relevant academic research and scientific papers

Characterization of equatorial and axial six-membered-ring peroxyl radicals

DiLabio, Gino A.,Ingold, Keith U.,Walton, John C.

, p. 8095 - 8098 (2008/02/13)

(Chemical Equation Presented) Spectroscopic data are consistent with computations that show that, in their most stable conformations, the peroxyl moiety is equatorial in cyclohexylperoxyl radicals and axial in oxa- and most polyoxacyclohexyl-2-peroxyl radicals.

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