S-(Thiobenzoyl)thioglycolic acid

99%

  • Product Code: 116111
  Alias:    2-Mercapto-S-thiobenzoylacetic acid
  CAS:    942-91-6
Molecular Weight: 212.29 g./mol Molecular Formula: C₆H₅CS₂CH₂CO₂H
EC Number: 213-393-0 MDL Number: MFCD00004927
Melting Point: 125-127 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: Used as a key intermediate in organic synthesis, particularly in the preparation of thiobenzamide derivatives. It plays a significant role in the production of pharmaceuticals, where it acts as a building block for active pharmaceutical ingredients (APIs). Additionally, it is utilized in the synthesis of agrochemicals, contributing to the development of pesticides and herbicides. Its thiocarbonyl group makes it valuable in coordination chemistry for creating metal complexes. In polymer chemistry, it is employed as a modifier or crosslinking agent to enhance material properties. It also finds application in biochemical research for studying enzyme inhibition and protein interactions.
Product Specification:
Test Specification
Melting Point 125-127
Purity (HPLC) 99-100
Purity (Neutralization Titration) 98.5-101.5
Appearance Carmine Crystals
Infrared Spectrum Conforms To Structure
Solubility In Acetone Almost Transparency
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,120.00
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5.000 10-20 days ฿3,950.00
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25.000 10-20 days ฿14,120.00
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S-(Thiobenzoyl)thioglycolic acid
Used as a key intermediate in organic synthesis, particularly in the preparation of thiobenzamide derivatives. It plays a significant role in the production of pharmaceuticals, where it acts as a building block for active pharmaceutical ingredients (APIs). Additionally, it is utilized in the synthesis of agrochemicals, contributing to the development of pesticides and herbicides. Its thiocarbonyl group makes it valuable in coordination chemistry for creating metal complexes. In polymer chemistry, it is employed as a modifier or crosslinking agent to enhance material properties. It also finds application in biochemical research for studying enzyme inhibition and protein interactions.
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