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Peroxide, bis([1,1'-biphenyl]-2-ylcarbonyl), also known as bis(4-biphenylcarbonyl) peroxide, is an organic compound with the chemical formula C30H18O4. It is a white crystalline solid that is widely used as a polymerization initiator, particularly in the production of polystyrene and other vinyl polymers. This peroxide is known for its high efficiency and ability to generate free radicals at relatively low temperatures, which aids in the initiation of polymerization reactions. It is also characterized by its stability and low volatility, making it a preferred choice in industrial applications where safety and control over the polymerization process are crucial.

861-97-2

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861-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861-97-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 861-97:
(5*8)+(4*6)+(3*1)+(2*9)+(1*7)=92
92 % 10 = 2
So 861-97-2 is a valid CAS Registry Number.

861-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-phenylbenzoyl) 2-phenylbenzenecarboperoxoate

1.2 Other means of identification

Product number -
Other names bis(2-phenylbenzoyl) 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:861-97-2 SDS

861-97-2Relevant academic research and scientific papers

Reactions of Carboxylic Acid Derivatives with Superoxide

Forrester, Alexander R.,Purushotham, Vemeshetti

, p. 945 - 951 (2007/10/02)

The mechanisms of the reactions of superoxide with carboxylic esters, acyl peroxides, and the acyl chlorides of α- and β-bromocarboxylic acids have been investigated.Experimental evidence is presented supporting the view that (a) conversion of an ester into its carboxylic acid does not proceed via the corresponding acyl peroxide; (b) conversion of acyl peroxide into carboxylic acid by superoxide involves either electron transfer to or an SN2 reaction on the peroxidic group; (c) α-bromoacyl chlorides with superoxide give the corresponding aldehyde via a cyclic peroxidic intermediate.

Mechanism of Hydrolysis of Esters by Superoxide

Forrester, Alexander R.,Purushotham, Vemishetti

, p. 1505 - 1506 (2007/10/02)

Experimental evidence is presented indicating that hydrolysis of an ester by superoxide in an aprotic solvent does not proceed via the corresponding acyl peroxide, although the peroxycarboxylate anion is involved.

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