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Details

Stereochemistry ACHIRAL
Molecular Formula C22H30O2S
Molecular Weight 358.537
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-THIOBIS(2-TERT-BUTYL-5-METHYLPHENOL)

SMILES

CC1=CC(O)=C(C=C1SC2=C(C)C=C(O)C(=C2)C(C)(C)C)C(C)(C)C

InChI

InChIKey=HXIQYSLFEXIOAV-UHFFFAOYSA-N
InChI=1S/C22H30O2S/c1-13-9-17(23)15(21(3,4)5)11-19(13)25-20-12-16(22(6,7)8)18(24)10-14(20)2/h9-12,23-24H,1-8H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A proton spin-lattice relaxation rate study of methyl and t-butyl group reorientation in the solid state.
2010-07
Endocrine disruptive effects of chemicals eluted from nitrile-butadiene rubber gloves using reporter gene assay systems.
2008-03
Identification of phenolic dermal sensitizers in a wound closure tape.
2007-10
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Male reproductive toxicity of four bisphenol antioxidants in mice and rats and their estrogenic effect.
2006-04
Chemical-induced atrial thrombosis in NTP rodent studies.
2005
Steroid hormone activity of flavonoids and related compounds.
2000-07
Patents
Name Type Language
SANTONOX
HSDB  
Preferred Name English
4,4'-THIOBIS(2-TERT-BUTYL-5-METHYLPHENOL)
Systematic Name English
SUMILIZER WX
Brand Name English
4,4-THIO-BIS-2-TERTBUTYL-5-METHYLPHENOL
Common Name English
4,4'-THIOBIS(6-TERT-BUTYL-M-CRESOL)
Systematic Name English
THIO-BIS-2-TERTBUTYL-5-METHYLPHENOL
Common Name English
ULTRANOX 236
Brand Name English
NSC-35388
Code English
LOWINOX 44S36
Brand Name English
THIOBIS(6-TERT-BUTYL-M-CRESOL), 4,4'-
Systematic Name English
SANTONOX [HSDB]
Common Name English
Code System Code Type Description
EVMPD
SUB77729
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
SMS_ID
100000138279
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
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EPA CompTox
DTXSID4021341
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
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FDA UNII
3CA5G9822V
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
HSDB
5304
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
PUBCHEM
7308
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
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NSC
35388
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
CAS
96-69-5
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-525-2
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY