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3,3-ditert-butyl-5,5-dimethyl[1,1-biphenyl]-4,4-diol, also known as BHT or butylated hydroxytoluene, is a synthetic organic compound widely used as an antioxidant and preservative in various industries. This chemical compound is characterized by its molecular formula C15H24O2 and a molecular weight of 236.35 g/mol. BHT is particularly effective in preventing the oxidation of fats and oils, making it a common additive in food products, cosmetics, and pharmaceuticals. It is also used in the rubber and petroleum industries to extend the shelf life of products and protect them from degradation. The compound's structure, with two tert-butyl groups and two methyl groups attached to a biphenyl core, contributes to its stability and effectiveness as an antioxidant. Despite its widespread use, BHT's safety has been a subject of debate, with some studies suggesting potential health risks, while others support its use within regulated limits.

3432-00-6

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3432-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3432-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3432-00:
(6*3)+(5*4)+(4*3)+(3*2)+(2*0)+(1*0)=56
56 % 10 = 6
So 3432-00-6 is a valid CAS Registry Number.

3432-00-6SDS

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-tert-butyl-4-(3-tert-butyl-4-hydroxy-5-methylphenyl)-6-methylphenol

1.2 Other means of identification

Product number -
Other names 2,2'-dimethyl-6,6'-di-tert-butyl-4,4'-biphenol

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:3432-00-6 SDS

3432-00-6Relevant academic research and scientific papers

Mushroom tyrosinase catalysed coupling of hindered phenols: A novel approach for the synthesis of diphenoquinones and bisphenols

Pandey,Muralikrishna,Bhalerao

, p. 3771 - 3774 (1990)

An efficient oxidative carbon-carbon coupling of hindered phenols leading to diphenoquinones and bisphenols by mushroom tyrosinase is reported.

Selective oxidation of phenols to hydroxybenzaldehydes and benzoquinones with dioxygen catalyzed by polymer-supported copper

Takaki, Ken,Shimasaki, Yohei,Shishido, Tetsuya,Takehira, Katsuomi

, p. 311 - 317 (2007/10/03)

Oxidation of 2,6-disubstituted 4-methylphenols with dioxygen by using a CuCl2-poly(4-methyl-4′-vinyl-2,2′-bipyridine) catalyst gave the corresponding 4-hydroxybenzaldehydes in high yields. The activity of the catalyst and the selectivity of the products significantly depended on the reaction conditions and the composition of the catalyst. When the molar ratio of the bipyridine unit of the polymer ligand to Cu was unity, i.e., N/Cu = 2, the best results were obtained. Moreover, the reaction is likely to be promoted by coordination of the products to the catalyst. Similarly, 2,3,6-trimethylphenol and related compounds were converted to p-benzoquinones selectively with a CuCl2-poly(4-vinylpyridine) catalyst. These polymer-supported catalysts were readily recovered and are reusable without noticeable decrease of their activity.

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