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4-MERCAPTOPHENYLACETIC ACID

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4-MERCAPTOPHENYLACETIC ACID Basic information

Product Name:
4-MERCAPTOPHENYLACETIC ACID
Synonyms:
  • 4-MERCAPTOBENZENEACETATE
  • 4-MERCAPTOPHENYLACETIC ACID
  • 4-Mercaptophenylacetic Acid ( MPAA)
  • 2-(4-sulfanylphenyl)acetic acid
  • MPAA
  • 4-Mercaptophenylacetic acid 97%
  • 4-Mercaptophenylacetic acid≥ 98% (HPLC)
  • Benzeneacetic acid,4-mercapto-
CAS:
39161-84-7
MF:
C8H8O2S
MW:
168.21
Product Categories:
  • Aromatic Phenylacetic Acids and Derivatives
  • Intermediates
  • Sulfur & Selenium Compounds
  • Organic Building Blocks
  • Sulfur Compounds
  • Thiols/Mercaptans
Mol File:
39161-84-7.mol
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4-MERCAPTOPHENYLACETIC ACID Chemical Properties

Melting point:
105-109 °C (lit.)
Boiling point:
336.0±17.0 °C(Predicted)
Density 
1.299±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Acetonitrile (Slightly), DMSO (Slightly)
pka
4.21±0.10(Predicted)
form 
Solid
color 
Off-White
Water Solubility 
Slightly soluble in water. Soluble in Dichloromethane, Ethanol and Methanol
Sensitive 
Air Sensitive
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Safety Information

Hazard Codes 
Xi
Risk Statements 
37/38-41
Safety Statements 
26-36/37/39
RIDADR 
UN 3335
WGK Germany 
3
HS Code 
2930909899

MSDS

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4-MERCAPTOPHENYLACETIC ACID Usage And Synthesis

Chemical Properties

4-MERCAPTOPHENYLACETIC ACID is White Powder

Uses

4-MERCAPTOPHENYLACETIC ACID is a redox buffer that increases the folding rate of disulfide-containing proteins realative to traditional buffers such as glutathione and glutathione-disulfide. A useful synthetic intermediate for the preparation of novel antiinflammatory agents.

Uses

4-Mercaptophenylacetic acid has been used in the preparation of small ubiquitin-like modifier peptides from bis(2-sulfanylethyl)amido peptide via sequential native chemical ligation.
It can be used:

  • On-resin preparation of peptide-α thiophenylesters which are used in a chemical ligation process for the chemical synthesis of peptides.
  • In one pot deprotection of (acetamido-methyl)cysteine following native chemical ligation and/or desulfurization method for the preparation of peptides.
  • Palladium facilitated deprotection of N-terminal cysteine through native chemical ligation method for the preparation of synthetically challenging proteins.

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