4-tert-Butylbenzenethiol
99%
Reagent
Code: #118872
Alias
4-tert-Butylthiophenol
CAS Number
2396-68-1
blur_circular Chemical Specifications
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Molecular Information
Weight
166.28 g/mol
Formula
CH₃₃CC₆H₄SH
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Registry Numbers
EC Number
219-255-6
MDL Number
MFCD00022067
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Physical Properties
Melting Point
-11 °C
Boiling Point
238 °C(lit.)
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Storage & Handling
Density
0.964 g/mL at 25 °C(lit.)
Storage
room temperature, sealed
description 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.
format_list_bulleted Product Specification
Test Parameter | 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 |
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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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