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2-ethylhexyl [[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]thio]acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80387-97-9

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80387-97-9 Usage

Safety Profile

An experimental teratogen. Otherexperimental reproductive effects. When heated todecomposition it emits toxic fumes of SOx.

Check Digit Verification of cas no

The CAS Registry Mumber 80387-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,8 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80387-97:
(7*8)+(6*0)+(5*3)+(4*8)+(3*7)+(2*9)+(1*7)=149
149 % 10 = 9
So 80387-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H42O3S/c1-9-11-12-18(10-2)15-28-22(26)17-29-16-19-13-20(24(3,4)5)23(27)21(14-19)25(6,7)8/h13-14,18,27H,9-12,15-17H2,1-8H3

80387-97-9SDS

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 2-ethylhexyl [[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]thio]acetate

1.2 Other means of identification

Product number -
Other names Irganox 1192

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:80387-97-9 SDS

80387-97-9Downstream Products

80387-97-9Relevant academic research and scientific papers

Catalytic thioalkylation of phenols based on mannich-type phenol

Liu, Peng,Zhu, Lunyu,Fang, Yan,Zhang, Huaiping,Chen, Dehong,He, Tao,Chen, Mingcai,Xu, Kai

, p. 2609 - 2613 (2008/02/10)

A thioalkylation of phenols involving reactive phenols, aldehydes, and thiols is described under Mannich-type phenol catalysis to afford thiomethyl phenols in good yields. Copyright Taylor & Francis Group, LLC.

Process for producing phenolic thiocarboxylic esters

-

, (2008/06/13)

Compounds of the formula I STR1 wherein R1 and R2 independently of one another are each tert-butyl, R3 is C1 -C20 -alkyl, or C2 -C20 -alkyl interrupted by --O-- or --S--, and n i

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