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Phenol, 4-[(2-benzothiazolylthio)methyl]-2,6-bis(1,1-dimethylethyl)-, also known as 2,6-di-tert-butyl-4-(benzothiazol-2-ylthiomethyl)phenol, is a complex organic compound with the chemical formula C23H27NOS. It is a derivative of phenol, featuring a benzothiazole ring attached to the phenol backbone through a sulfur atom. The compound is characterized by its two tert-butyl groups (1,1-dimethylethyl) at the 2 and 6 positions of the phenol ring, which contribute to its stability and lipophilic nature. This chemical is primarily used as an antioxidant in various industrial applications, including the stabilization of polymers and lubricants, to prevent oxidative degradation and extend their service life. Its unique structure endows it with the ability to scavenge free radicals and protect materials from the damaging effects of oxidation.

6029-97-6

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6029-97-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6029-97-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6029-97:
(6*6)+(5*0)+(4*2)+(3*9)+(2*9)+(1*7)=96
96 % 10 = 6
So 6029-97-6 is a valid CAS Registry Number.

6029-97-6SDS

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 4-(1,3-benzothiazol-2-ylsulfanylmethyl)-2,6-ditert-butylphenol

1.2 Other means of identification

Product number -
Other names Phenol,4-[(2-benzothiazolylthio)methyl]-2,6-bis(1,1-dimethylethyl)

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:6029-97-6 SDS

6029-97-6Relevant academic research and scientific papers

Reactions of benzazole-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

Tagasheva,Gataullina,Zaripova,Bukharov,Nugumanova,Deberdeev,Voronina, Yu. K.

, p. 22 - 28 (2017/07/07)

The benzylation of benzothiazole(oxazole, imidazole)-2-thiones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate involves either the sulfur or nitrogen atom depending on the reaction conditions. The S- and N-benzylation products of benzazole-2-thiones are kinetically and thermodynamically controlled products, respectively. The use of 3,5-di-tert-butyl-4-hydroxy-benzyl acetate allows sterically hindered hydroxybenzyl derivatives of benzаzole-2-thiones to be generally synthesized under milder conditions than in known methods of their synthesis.

Antiradical activity of benzazole-2-thiones

Gataullina,Mogilevtseva,Nugumanova,Bukharov,Tagasheva,Deberdeev, R. Ya.

, p. 1919 - 1923 (2017/10/27)

Reaction of benzoxazole-2-thione with 3,5-di-tert-butyl-4-hydroxybenzylacetate in methanol affords S-(3,5-di-tert-butyl-4-hydroxybenzyl)-2-mercaptobenzoxazole as the major product. Antiradical activity of S- and N-3,5-di-tert-butyl-4-hydroxybenzyl derivatives of benzothiazole(oxazole, imidazole)-2-thione with respect to 2,2-diphenyl-1-picrylhydrazyl is varies widely. S-Benzyl derivatives exhibit higher reactivity at 30°C.

Acetyl chloride - 3,5-di(tert-butyl)-4-hydroxy-N,N-dimethylbenzylamine salt in the benzylation of organic and inorganic sulfur-containing compounds

Gorbunov, D. B.,Voznesenskii, V. N.,Ershov, V. V.,Nikiforov, G. A.

, p. 93 - 97 (2007/10/02)

The reactions of the quaternary acylammonium salt formed on treatment of 3,5-di-tert-butyl-4-hydroxy-N,N-dimethylbenzylamine with acetyl chloride, with various organic and inorganic sulfur-containing compounds were studied.The possibility of using this salt for the introduction of a sterically hindered phenol moiety in various sulfur-containing compounds was shown. - Key words: sterically hindered phenols, quaternary ammonium salts, benzylation, thiourea.

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