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2-Propeneperoxoic acid, 1,1-dimethylethyl ester, also known as tert-butyl peroxyisobutyrate or TBPB, is a colorless liquid organic compound with the chemical formula C8H14O3. It is a type of peroxide, specifically a peroxyester, and is used as a crosslinking agent in the production of polymers, particularly in the manufacturing of polyethylene and polypropylene. TBPB is also employed as a curing agent for unsaturated polyester resins and as a catalyst in various chemical reactions. Due to its peroxide nature, it is highly reactive and can be hazardous, necessitating careful handling and storage to prevent decomposition and potential explosions.

4161-71-1

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4161-71-1 Usage

Physical properties

Colorless and oily liquid with a pungent odor

Chemical reactivity

Highly reactive due to the presence of the peroxy functional group

Main uses

Radical initiator in polymerization and crosslinking reactions, production of polymers and resins, manufacturing of adhesives, coatings, and elastomers

Safety precautions

Handle with caution, health hazards present, use in well-ventilated area with appropriate personal protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 4161-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,6 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4161-71:
(6*4)+(5*1)+(4*6)+(3*1)+(2*7)+(1*1)=71
71 % 10 = 1
So 4161-71-1 is a valid CAS Registry Number.

4161-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl peracrylate

1.2 Other means of identification

Product number -
Other names tert.-Butyl-peracrylat

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:4161-71-1 SDS

4161-71-1Downstream Products

4161-71-1Relevant academic research and scientific papers

Reaction of unsaturated esters with the oxidative system aluminum tri-tert-butoxide-tert-butyl hydroperoxide

Stepovik,Martynova,Dodonov

, p. 1225 - 1229 (2007/10/03)

Unsaturated esters containing double bonds in the acyl (methyl acrylate) or in the alcohol (vinyl and allyl acetates) fragments are cleaved under mild conditions (20°C) by the system aluminum tri-tert-butoxide-tert-butyl hydroperoxide to give tert-butyl esters of peroxycarboxylic acids and unsymmetrical aluminum alkoxides. The double bond in the acyl fragment is inert to this oxidation system. Vinyloxy- and allyloxy derivatives are oxidized to hydroxyethanal and (hydroxymethyl)oxirane, respectively. Carbon-hydrogen bonds are oxidized only in allyl acetate.

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