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

43079-24-9

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43079-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 43079-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,7 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 43079-24:
(7*4)+(6*3)+(5*0)+(4*7)+(3*9)+(2*2)+(1*4)=109
109 % 10 = 9
So 43079-24-9 is a valid CAS Registry Number.

43079-24-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(α-hydroxy-isobutoxy)-2,2,4-trimethyl-valeraldehyde

1.2 Other means of identification

Product number -
Other names 3-(α-Hydroxy-isobutoxy)-2,2,4-trimethyl-valeraldehyd

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:43079-24-9 SDS

43079-24-9Relevant academic research and scientific papers

Antioxidants and process of preparing said antioxidants

-

, (2008/06/13)

Phenolic antioxidants such as 1,1-dimethyl-2-(3,5-di tert.butyl-4-hydroxyphenyl) ethyl amine and a method of preparing said antioxidants involving the reaction between a 3,5-di tert.alkyl-4-hydroxybenzyl halide; N,N-dialkyl amine or dithiocarbamate such a

Nitroalkane based hindered phenol compounds and methods of preparation thereof

-

, (2008/06/13)

There are disclosed, as novel compounds, high molecular weight hindered phenols based on the condensation of a nitroalkane with either formaldehyde and di-t-butylphenol or with a substituted derivative of a di-t-butylphenol. The compounds are generally us

Nitroalkane based hindered phenol compounds and preparation thereof

-

, (2008/06/13)

There are disclosed, as novel compounds, high molecular weight hindered phenols based on the condensation of a nitroalkane with either formaldehyde and a di-t-butylphenol or with a substituted derivative of a di-t-butylphenol. The compounds are generally

Method of preparing phenolic antioxidants by condensing active methylene compounds with 3,5-di-tert alkyl-4-hydroxybenzylpyridinium salts

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, (2008/06/13)

3,5-Di-tert alkyl-4-hydroxybenzylpyridinium salts are reacted under basic conditions with compounds containing active methylene groups to form phenolic antioxidants. For example, 3,5-di-tert.butyl-4-hydroxybenzylpyridinium chloride is reacted with 2-nitro

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