3273-24-3

Basic information

• Product Name: o,o-p-tert-Butylphenol monosulfide
• CAS NO: 3273-24-3
• Molecular Formula: C₂₀H₂₆O₂S
• Molecular Weight: 330.491
• Mol File: 3273-24-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: o,o-p-tert-Butylphenol monosulfide(CAS DataBase Reference)
• NIST Chemistry Reference: o,o-p-tert-Butylphenol monosulfide(3273-24-3)
• EPA Substance Registry System: o,o-p-tert-Butylphenol monosulfide(3273-24-3)

Safety Data

• Hazardous Substances Data: 3273-24-3(Hazardous Substances Data)

Upstream product

• 98-54-4 para-tert-butylphenol 
• 56-81-5 glycerol 

Downstream Products

• 1034120-00-7 bis[5-tert-butyl-2-(trifluoromethylsulfonyloxy)phenyl]sulfan 
• 133786-62-6 4-tert-butyl-2-(5-tert-butyl-2-hydroxyphenylsulfanyl)-6-(hydroxymethyl)phenol 
• 133786-63-7 4,4'-di(tert-butyl)-2,2'-bis(hydroxymethyl)-6,6'-sulfandiyldiphenol 
• 25247-32-9 C₂₀H₂₆O₄S 
• 1119828-91-9 C₂₂H₂₆O₄S 
• 133785-88-3 2-<3-<3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butylsalicyl>-5-t-butyl-2-hydroxyphenylthio>-4-t-butylphenol 
• 133785-90-7 2-<3-<3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butylsalicyl>-5-t-butylsalicyl>-4-t-butylphenol 
• 133785-89-4 2-<3-<3-(5-t-butylsalicyl)-5-t-butyl-2-hydroxyphenylthio>-5-t-butylsalicyl>-4-t-butylphenol 
• 56857-30-8 2-<3-<3-(5-t-butyl-2-hydroxyphenylthio)-5-t-butyl-2-hydroxyphenylthio>-5-t-butyl-2-hydroxyphenylthio>-4-t-butylphenol 

Relevant articles and documents

Effect of ionizing radiation on the extraction of Am(III) with p-tert-butylthiacalix[4]arene from alkaline carbonate solutions

The effect of γ-irradiation of tert-butylthiacalix[4]arene (TCA) solutions in m-nitrobenzotrifluoride (NBTF) and tetrachloroethylene (TCE) on the extraction of 241Am from alkaline carbonate solutions was studied. TCA itself remains stable upon γ-irradiation of its solutions in NBTF to a dose of 200 kGy, but the diluent undergoes strong degradation. The radiation resistance of TCA in TCE is considerably lower: A dose of 70 kGy causes complete degradation of TCA. In the TCA–TCE–aqueous phase system, sulfate ions appear upon γ-irradiation as the final product of the extractant radiolysis. A large number of γ-radiolysis products of TCE and TCA were detected by HPLC and GCMS. The products of radiolysis of TCA in TCE, compared to the initial extractant, have lower molecular mass and higher polarity. The results show that chlorinated diluents are not promising diluents for thiacalixarene in extraction processing of alkaline high-level waste.

Synthesis and Inclusion Properties of Sulfur-Bridged Analogs of Acyclic Phenol-Formaldehyde Oligomers

A series of compounds in which a part or all of the methylene bridges of acyclic p-methyl- and p-t-butylphenol-formaldehyde tetramers were replaced by sulfur bridge(s) was synthesized.It was found that though the sulfur-bridged tetramers formed crystalline host-guest complexes with a variety of organic compounds, they were different from the parent tetramers regarding their inclusion behavior.The number and position of the sulfur bridge(s), as well as the p-substituent of phenol in the tetramers, had a great influence upon the inclusion property.The thermal stability of complexes of the sulfur-bridged tetramers (SSS-a,b) with benzene, as estimated from their thermal dissociation rates, are lower than those of the parent tetramers (CCC-a,b).