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Ethanol, 1-[(1,1-dimethylethyl)dioxy]-, benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76387-34-3

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76387-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76387-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,8 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76387-34:
(7*7)+(6*6)+(5*3)+(4*8)+(3*7)+(2*3)+(1*4)=163
163 % 10 = 3
So 76387-34-3 is a valid CAS Registry Number.

76387-34-3SDS

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 benzoic acid,1-tert-butylperoxyethanol

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:76387-34-3 SDS

76387-34-3Relevant academic research and scientific papers

Synthesis of α-hydroxyalkyl peroxide esters and ethers as initiators of radical processes

Aleinikova,Navrotskii

, p. 1890 - 1900 (2014)

α-Hydroxyalkyl peroxide esters and ethers containing, along with the peroxy bond, also acyloxy and alkoxy groups, are effective initiators of radical processes. The initiation efficiency is due to the capability of these molecules to generate simultaneously oxygen- and carbon-centered radicals capable of hydrogen abstraction from the substrate and of addition to C=C bonds. The selectivity of the synthesis of α-hydroxyalkyl peroxide esters and ethers is mainly determined by the steps of the synthesis and isolation of the intermediate α-chloroalkyl peroxides, because of their high reactivity. Experimental conditions allowing control of the synthesis of α-hydroxyalkyl peroxide esters and ethers were found.

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