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4,4',6,6'-Di-tert-butyl-2,2'-thiobisphenol, also known as bisphenol A bis(2-tert-butyl-4-methylphenol), is a chemical compound with the molecular formula C31H42O2S. It is a white crystalline solid that is widely used as an antioxidant and a stabilizer in the production of polycarbonate plastics, epoxy resins, and other polymers. 4,4',6,6'-DI-TERT-BUTYL-2,2'-THIOBISPHENOL is known for its ability to prevent the oxidation of polymers, thereby extending their shelf life and improving their performance. It is also used in the synthesis of certain pharmaceuticals and agrochemicals. Due to its chemical structure, it is resistant to heat and light, which makes it suitable for applications where stability under harsh conditions is required.

3293-91-2

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3293-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3293-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3293-91:
(6*3)+(5*2)+(4*9)+(3*3)+(2*9)+(1*1)=92
92 % 10 = 2
So 3293-91-2 is a valid CAS Registry Number.

3293-91-2SDS

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 2,2'-thiobis[4,6-bis(1,1-dimethylethyl)phenol]

1.2 Other means of identification

Product number -
Other names 2,2'-thiobis(2,4-di-tert-butylphenole)

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:3293-91-2 SDS

3293-91-2Relevant academic research and scientific papers

Medium-sized organogermanium heterocycles containing a transannular sulfur atom: First synthesis and characterization of a sterically hindered eight-membered 1 2H-dibenzo[d,g] [13,6,2]dioxathiagermocin

Pastor, Stephen D.,Huang, Victor,Nabirahni, David

, p. 87 - 96 (1998)

The synthesis and characterization of a sterically hindered eight-membered 12H-dibenzo[d,g][1 ,3,6,2]dioxathiagermocin is described. The ΔG$273 for ring inversion (12.8 kcal.mol-1) was determined by variable temperature1H

Novel reactivity of side-on (disulfido)dicopper complexes supported by bi- and tridentate nitrogen donors: Impact of axial coordination

Bar-Nahum, Itsik,York, John T.,Young Jr., Victor G.,Tolman, William B.

, p. 533 - 536 (2008/09/21)

(Figure Presented) What a difference a ligand makes: A comparison of the reactivity of the two complexes shown (Cu green, S yellow, N blue, O red, F pink, C gray) has revealed new redox processes previously unseen for copper-sulfur complexes. Furthermore, intriguing supporting-ligand effects on the properties of (disulfido)dicopper cores are uncovered.

Ethylene oxide polymerization catalyzed by aluminum complexes of sulfur-bridged polyphenols

Wasserman, Eric P.,Annis, Ioana,Chopin III, Lamy J.,Price, Philip C.,Petersen, Jeffrey L.,Abboud, Khalil A.

, p. 322 - 333 (2007/10/03)

The products derived from the reaction of sterically hindered sulfur-bridged bisphenols with aluminum trialkyls enable the efficient polymerization of ethylene oxide. The activity of the catalyst is largely determined by the structure of the bisphenol lig

Organoaluminum catalyst

-

Page/Page column 6-7, (2010/02/07)

An organoaluminum reaction product of A.) a ligand of the formula I, wherein R1 represents an alkyl, aryl, arylalkyl, or alkylaryl group, a C3-24 silyl group, or hydrogen, R2, R3, R4, R5, R6, R7, R12, and R13 are the same or different and represent an alkyl, aryl, arylalkyl, or alkylaryl group, a C3-24 silyl group, halide, or hydrogen, with the proviso that at least one of the groups R4 and R13 represents hydrogen, R8 represents an alkoxy, alkyl, aryl, arylalkyl, or alkylaryl group, a C3-24 silyl group, halide, hydroxyl radical, or hydrogen, E represents O, S, Se, or Te, and n is an integer from 1 to 4, and B.) an aluminum compound of formula AlR9R10R11, wherein R9 and R10 are the same or different and represent C1-20 alkyl, aryl, arylalkyl, or alkylaryl group, or hydrogen, and R11 is a C1-20 alkyl, aryl, arylalkyl, alkylaryl or alkoxy group, hydrogen, or halogen is useful as a polymerization catalyst, particularly for the homopolymerization or copolymerization of an alkylene oxide.

Eight-Membered Organosulphur Heterocycles. Synthesis of Dibenzodioxathiaphosphocin and Dibenzodioxathiasilocin Ring System

Pastor, Stephen D.,Spivack, John D.,Steinhuebel, Leander P.

, p. 1285 - 1287 (2007/10/02)

The reaction of 2,2'-thiobisphenols with either phenylphosphonous dichloride or phosphorus trichloride followed by an alcohol gave derivatives of the dibenzodioxathiaphosphocin ring system.The analogous reaction of 2,2'-thiobisphenols with a

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