3-mercaptopropionic acid pharmaceutical grade

Description:

3-mercaptopropionic acid, also known as β - mercaptopropionic acid, with the chemical formula C ∝ H ₆ O ₂ S, is a colorless and transparent liquid with a special odor. Its molecular structure contains both carboxyl and thiol groups, which endows it with unique chemical properties and makes it play an important role in many fields....


  • Melting point 15-18 ℃ (lit.)
  • Boiling 110-111 ℃/15 mmHg (lit.)
  • Densities 1.218 g/mL at 25 ℃ (lit.)
  • Color Colorless to light yellow
  • Morphological Fluids
  • Wrap 250kg/1000kg plastic drum
  • Stability Air sensitive, hygroscopic

Product details

Application

Ultra-high purity standard

Purity ≥99.5% (HPLC test), mercaptan content (-SH) ≥99.0%, moisture content ≤0.1%, heavy metal content ≤1ppm (in accordance with USP/EP standard)

Excellent chemical properties

Molecular formula: C3H6O2S, Molecular weight: 106.14, Boiling point: 110-112°C (10mmHg), Flash point: >110°C, Density: 1.218 g/cm³ (25°C)

Special Quality Assurance

Colorless to slightly yellow transparent liquid, characteristic mercaptan odor (can be reduced by special process), peroxide content ≤10ppm, residual solvent content ≤0.05%

Stability performance

Long-term stability under nitrogen protection, recommended storage temperature 2-8°C, sealed and protected from light storage period ≥ 24 months

Application Performance Advantages

Excellent coordination ability (forming stable complexes with metal ions), efficient free radical trapping ability, good water solubility and organic solvent compatibility,

controllable reactivity (pH-dependent)

Special Processing

Molecular distillation purification technology, low-temperature inert gas protection production process, three-stage filtration and purification system (0.2μm terminal filtration)

Quality Approvals

Compliance with USP/EP/JP Pharmacopoeia standards, ISO 9001:2015 quality management certification, REACH registration completed, complete COA/MSDS documentation

provided.


Pharmaceutical synthesis intermediates

Synthesis of sulfur-containing drugs: captopril, N-acetylcysteine (NAC) derivatives, anticancer drugs

Antibiotic modifications: cephalosporin antibiotics, beta-lactamase inhibitors

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Protein and Antibody Engineering

protein modification (thiol-disulfide bond exchange): antibody-drug coupling (ADC), polyethylene glycolization (PEGylation)

Fluorescent labeling and diagnostics: binding of proteins via sulfhydryl groups for immunoassays (e.g. ELISA) or cellular imaging.

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Antioxidant and cell protection

Glutathione (GSH) analog synthesis, heavy metal detoxifier

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Other Pharmaceutical Applications

Medical adhesives, dental materials

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