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1,2-Benzenediol, 4,6-bis(1,1-dimethylethyl)-3-[(2-hydroxyethyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93154-91-7

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93154-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93154-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,5 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93154-91:
(7*9)+(6*3)+(5*1)+(4*5)+(3*4)+(2*9)+(1*1)=137
137 % 10 = 7
So 93154-91-7 is a valid CAS Registry Number.

93154-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-ditert-butyl-3-(2-hydroxyethylsulfanyl)benzene-1,2-diol

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:93154-91-7 SDS

93154-91-7Downstream Products

93154-91-7Relevant academic research and scientific papers

Synthesis and Antioxidant Activity of Sulfur-containing Derivatives of 3,5-Di-tert-butyl-1,2-benzenediol

Maslovskaya,Petrikevich,Timoshchuk,Shadyro

, p. 1847 - 1850 (2007/10/03)

3-Alkylthio-4,6-di-tert-butyl-1,2-benzenediols have been synthesized by addition of thiols to 3,5-di-tert-butyl-1,2-benzenediol. Their antiradical and and antioxidant activities were estimated using the model of γ-irradiation-initiated oxidation of hexane. The antiradical activity of 4,6-di-tert-butyl-7-hydroxy-1,3-benzoxathiole-2-thione, which is an ortho analog of tocopherol with a five-membered ring, is 7 times higher than that of the six-membered analog, 5,7-di-tert-butyl-8-hydroxy-2,3-dihydro-1,4-benzooxatiin-2-one.

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