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Benzamide, N,N-bis[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-, also known as Bisphenol A bis(2-hydroxyethyl)ether bis(2-methoxyethyl)ether, is a complex organic compound with the chemical formula C27H38O5. It is a white crystalline solid that is soluble in most organic solvents. Benzamide, N,N-bis[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]- is primarily used as a curing agent for epoxy resins, which are widely employed in the production of composite materials, adhesives, and coatings. It plays a crucial role in enhancing the mechanical properties and thermal stability of these materials. Additionally, it has been used in the synthesis of polyurethane foams and as a stabilizer for PVC. However, due to concerns over its potential health and environmental impacts, there has been a growing interest in finding alternative curing agents.

89635-32-5

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89635-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89635-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89635-32:
(7*8)+(6*9)+(5*6)+(4*3)+(3*5)+(2*3)+(1*2)=175
175 % 10 = 5
So 89635-32-5 is a valid CAS Registry Number.

89635-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-bis(3,5-ditert-butyl-4-hydroxyphenyl)benzamide

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

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More Details:89635-32-5 SDS

89635-32-5Downstream Products

89635-32-5Relevant academic research and scientific papers

SYNTHESIS AND TRANSFORMATIONS OF BIRADICALS OF THE PHENOXYL SERIES

Ivakhnenko, E. P.,Shif, A. I.,Prokof'ev, A. I.,Khachatur'yan, G. A.,Olekhnovich, L. P.

, p. 528 - 533 (2007/10/02)

The mechanism of the one-electron oxidation of some derivatives of sterically hindered phenols was investigated by dynamic ESR method.The possibility of intramolecular homolytic recombination of the biradicals with the formation of nitrogen-containing het

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