3,5-Dimethylbenzenethiol

97%

  • Product Code: 117313
  Alias:    3,5-Dimethylthiophenol
  CAS:    38360-81-5
Molecular Weight: 138.23 g./mol Molecular Formula: C₈H₁₀S
EC Number: 253-901-8 MDL Number: MFCD00040226
Melting Point: Boiling Point: 127.5 °C50 mm Hg(lit.)
Density: 1.015 g/mL at 25 °C(lit.) Storage Condition: room temperature
Product Description: 3,5-Dimethylbenzenethiol is primarily used in organic synthesis as a building block for more complex chemical compounds. Its thiol group makes it a valuable reagent in the preparation of sulfur-containing molecules, which are often utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, it can serve as a ligand in coordination chemistry, aiding in the stabilization of metal complexes. The compound is also employed in the synthesis of polymers and resins, where its aromatic structure contributes to the material's stability and performance. In research, it is used to study reaction mechanisms involving sulfur-containing compounds.
Product Specification:
Test Specification
Purity (GC) 97-100
Refractive Index N20/D 1.567 Max
Specific Gravity (20/20 Degree Celsius) 1.014-1.016
Appearance Colorless To Yellow Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,260.00
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5.000 10-20 days ฿3,940.00
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25.000 10-20 days ฿15,780.00
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3,5-Dimethylbenzenethiol
3,5-Dimethylbenzenethiol is primarily used in organic synthesis as a building block for more complex chemical compounds. Its thiol group makes it a valuable reagent in the preparation of sulfur-containing molecules, which are often utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, it can serve as a ligand in coordination chemistry, aiding in the stabilization of metal complexes. The compound is also employed in the synthesis of polymers and resins, where its aromatic structure contributes to the material's stability and performance. In research, it is used to study reaction mechanisms involving sulfur-containing compounds.
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