4-tert-Butylbenzenethiol

99%

  • Product Code: 118872
  Alias:    4-tert-Butylthiophenol
  CAS:    2396-68-1
Molecular Weight: 166.28 g./mol Molecular Formula: CH₃₃CC₆H₄SH
EC Number: 219-255-6 MDL Number: MFCD00022067
Melting Point: -11 °C Boiling Point: 238 °C(lit.)
Density: 0.964 g/mL at 25 °C(lit.) Storage Condition: room temperature, sealed
Product Description: Used primarily as a chemical intermediate in the synthesis of various organic compounds. It is often employed in the production of antioxidants, stabilizers, and additives for polymers and plastics, enhancing their durability and performance. In the field of materials science, it serves as a key component in the development of self-assembled monolayers (SAMs) on metal surfaces, which are crucial for applications in nanotechnology and surface modification. Additionally, it finds use in the pharmaceutical industry as a building block for the synthesis of certain drugs and bioactive molecules. Its thiol group makes it valuable in coordination chemistry, where it acts as a ligand in the formation of metal complexes.
Product Specification:
Test Specification
Purity (GC) 99
Refractive Index N20/D 1.547-1.549
Specific Gravity (20/20) 0.988-0.99
Appearance Colorless To Yellow Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €10.29
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5.000 10-20 days €30.08
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25.000 10-20 days €118.46
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100.000 10-20 days €425.54
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4-tert-Butylbenzenethiol
Used primarily as a chemical intermediate in the synthesis of various organic compounds. It is often employed in the production of antioxidants, stabilizers, and additives for polymers and plastics, enhancing their durability and performance. In the field of materials science, it serves as a key component in the development of self-assembled monolayers (SAMs) on metal surfaces, which are crucial for applications in nanotechnology and surface modification. Additionally, it finds use in the pharmaceutical industry as a building block for the synthesis of certain drugs and bioactive molecules. Its thiol group makes it valuable in coordination chemistry, where it acts as a ligand in the formation of metal complexes.
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