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Catalog Number:
22299
CAS Number:
13095-73-3
Ácido 4-mercaptobutírico, grado técnico
Purity:
≥ 90% (GC)
Synonym(s):
Ácido 4-tiobutírico
Documents
$86.23 /1G
Tamaño
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Product Information

4-Mercaptobutyric acid, technical grade, is a versatile thiol compound known for its unique properties and applications in various industries. This compound, also referred to as 4-Sulfanylbutanoic acid, features a functional thiol group that enhances its reactivity, making it an excellent candidate for use in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. Its ability to form disulfide bonds allows it to play a crucial role in the stabilization of proteins and peptides, which is particularly beneficial in biochemistry and biotechnology research.

In addition to its applications in research, 4-Mercaptobutyric acid is utilized in the formulation of specialty chemicals and as a reagent in analytical chemistry. Its properties make it suitable for use in the development of antioxidants, surfactants, and corrosion inhibitors. Researchers and industry professionals appreciate its effectiveness in enhancing product performance and stability, making it a valuable addition to any chemical toolkit.

Synonyms
Ácido 4-tiobutírico
CAS Number
13095-73-3
Purity
≥ 90% (GC)
Molecular Formula
HSCH2CH2CH2CO2H
Molecular Weight
120.17
MDL Number
MFCD00053842
PubChem ID
25700
Appearance
Líquido transparente
Boiling Point
108-112 ºC a 3 mmHg
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-tiobutírico
CAS Number
13095-73-3
Purity
≥ 90% (GC)
Molecular Formula
HSCH2CH2CH2CO2H
Molecular Weight
120.17
MDL Number
MFCD00053842
PubChem ID
25700
Appearance
Líquido transparente
Boiling Point
108-112 ºC a 3 mmHg
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Mercaptobutyric acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a precursor for the synthesis of various pharmaceuticals, particularly in the development of drugs targeting metabolic disorders.
  • Biochemical Research: It is used in studies related to thiol chemistry, helping researchers understand protein interactions and enzyme functions due to its reactive sulfhydryl group.
  • Polymer Chemistry: The compound acts as a modifier in the production of polymers, enhancing properties such as flexibility and resistance to degradation, making it valuable in materials science.
  • Agricultural Applications: It is explored for use in developing plant growth regulators, promoting healthier crop yields and improving resistance to environmental stressors.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its antioxidant properties, helping to protect skin from oxidative damage and improve overall skin health.

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