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

71728-85-3

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71728-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71728-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,2 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71728-85:
(7*7)+(6*1)+(5*7)+(4*2)+(3*8)+(2*8)+(1*5)=143
143 % 10 = 3
So 71728-85-3 is a valid CAS Registry Number.

71728-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-ditert-butyl-4-(3-sulfanylpropyl)phenol

1.2 Other means of identification

Product number -
Other names 2,6-di-tert-butyl-4-(3-mercaptopropyl)phenol

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:71728-85-3 SDS

71728-85-3Relevant academic research and scientific papers

Mechanism of low-molecular alkenes interaction with sulfur-containing spatially hindered phenols under conditions of thermal modification of polymer materials

Krysin,Pokrovskii,Nefedov,Shundrina,Selivanov

, p. 659 - 666 (2015/05/05)

Abstract Transformations in the course of high-temperature modification of polyolefins under action of sulfur-containing modifiers have been studied using hexene-1 and hexane as model compounds. Composition of products of thermolysis of bis[3-(3,5-di-tert

Synthesis and antioxidative properties of new sulfur-containing derivatives of sterically hindered phenols

Prosenko,Terakh,Kandalintseva,Pinko,Gorokh,Tolstikov

, p. 1899 - 1902 (2007/10/03)

3-(3,5-Di-tert-butyl-4-hydroxyphenyl)-1-chloropropane was converted into derivatives containing S(II) in various functional groups. The inhibiting power of the compounds with respect to thermal autooxidation of animal fat was evaluated.

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