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4 tertbutylthiophenol

4-tertbutylthiophenol

4-tert-Butylbenzenethiol, 4-(1,1-dimethylethyl)benzenethiol, p-tert-Butylphenyl mercaptan, p-tert-Butylbenzenethiol, 4-tert-butylphenylthiol, Benzenethiol,p-tert-butyl, Benzenethiol,p-tert-butylthio, 4-t-Butylthiophenol, 4-tert-Butylthiophenol, 4-(1,1-dimethylethyl)thiophenol, 4-(tert-butyl)benzenethiol, Benzenethiol,4-(1,1-dimethylethyl) ,p-tert-Butylthiophenol

CAS No :

2396-68-1

EC Number :

219-255-6

Formula :

C10H14S

Categories: ,

Product Specification

  • Appearance & Physical State – clear colorless liquid
  • Molecular weight – 166.28300
  • Boiling point – 166.28300
  • Flash Point – 96.9ºC
  • Density – 0.964 g/mL at 25 °C
  • SMILES – CC(C)(C)c1ccc(S)cc1
  • Vapor Pressure – 0.0992mmHg at 25°C
  • Sensitive – Air Sensitive

Safety Information As Per GHS

Hazard Statement(s) as per GHS

  • H315: Causes skin irritation.
  • H319: Causes serious eye irritation
  • H335: May cause respiratory irritation
4-Tertbutylthiophenol4-tert-Butylphenol can be described as a phenol derivative. Contact with skin can cause leukoderma. It is extensively used within the industry of polymers. Reaction of 4-tert-Butylphenol with mushroom tyrosinase has been reported to afford 4-t-butyl-o-benzoquinone and kinetics of this enzymatic reaction has been investigated.4-tert-Butylphenol can be used as a fuel and carbon source in the medium used for cultivation of Sphingobium fuliginis strains. 4-tert-Butylphenol can be used as a reagent for kinetic studies of hydroxylation of 4-tert-butylphenol through the tyrosinase of mushrooms. It can be utilized to make calix[7]arene. 4-tert-butyltoluene is an organic chemical. It is used primarily as a raw material in the commercial production of p-tert-butylbenzoic-acid, which is utilised in the manufacture of unsaturated polyesters and alkyd resins. 4-tert-butyltoluene is made in a closed process and then transported through the plant through pipes to a plant for processing in which it is completely transformed inside closed production facilities to secondary chemicals by industrial chemical synthesizing. According to the industry, there are no open-ended uses of 4-tertbutyltoluene. Based on the registered products of those of the Nordic nations, Finland, Sweden and Norway confirmed that the chemical is not recognized as a registered chemical. It is listed in the Swiss Product Register lists 4-tert-butyltoluene in two different products (as an adhesive or sealing agent as well as for auxiliary chemicals) that contain lower than 1 percent in both of the two products.

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