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Cumyl peroxypivalate(in solution,content≤77%) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23383-59-7

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23383-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23383-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23383-59:
(7*2)+(6*3)+(5*3)+(4*8)+(3*3)+(2*5)+(1*9)=107
107 % 10 = 7
So 23383-59-7 is a valid CAS Registry Number.

23383-59-7SDS

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 α,α-Dimethylbenzyl peroxypivalate

1.2 Other means of identification

Product number -
Other names -

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:23383-59-7 SDS

23383-59-7Relevant academic research and scientific papers

The Thermal Decomposition of 1-Methyl-1-phenylethyl 2,2-Dimethylperoxypropionate in Cumene

Komai, Takeshi,Kato, Kenji,Matsuyama, Kazuo

, p. 2641 - 2642 (2007/10/02)

The thermal decomposition of 1-methyl-1-phenylethyl 2,2-dimethylperoxypropionate was studied in cumene.Based on the kinetic parameters and the decomposition products, it was concluded that the peroxyester was decomposed mainly by means of the radical process in cumene.

Batch process for manufacturing and purifying liquid organic peroxide by distillation

-

, (2008/06/13)

A batch process for the manufacture of liquid organic peroxides, such as peroxy esters and diacyl peroxides, by reacting an acid chloride, a hydroperoxide and an alkali metal hydroxide uses a countercurrent, packed distillation column for recovering a purer, drier product with higher yield than previous batch drying processes.

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