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Catalog Number:
07071
CAS Number:
2002-22-4
2-Mercapto-L-histidine
Purity:
≥ 98% (TLC)
Synonym(s):
L-His(2-mercapto)-OH
Documents
$106.96 /100MG
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Product Information

2-Mercapto-L-histidine is a versatile thiol compound known for its unique properties and applications in various fields, particularly in biochemistry and pharmaceuticals. This compound, a derivative of histidine, features a sulfhydryl group that enhances its reactivity and makes it an excellent candidate for redox reactions. Its ability to act as a reducing agent allows it to stabilize proteins and peptides, making it invaluable in the study of enzyme activity and protein folding. Researchers often utilize 2-Mercapto-L-histidine in the synthesis of metal complexes, which can be applied in catalysis and as potential therapeutic agents.

In addition to its role in research, 2-Mercapto-L-histidine has shown promise in the development of antioxidant formulations due to its capacity to scavenge free radicals. This characteristic positions it as a beneficial additive in cosmetic and pharmaceutical products aimed at enhancing skin health and combating oxidative stress. With its multifaceted applications, 2-Mercapto-L-histidine stands out as a crucial compound for professionals seeking innovative solutions in their respective fields.

Synonyms
L-His(2-mercapto)-OH
CAS Number
2002-22-4
Purity
≥ 98% (TLC)
Molecular Formula
C6H9N3O2S
Molecular Weight
187.2
MDL Number
MFCD00047018
PubChem ID
3037745
Appearance
Slightly yellow powder
Optical Rotation
[a]D24 = -10 ± 2 º (C=1 in 1M HCl)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
L-His(2-mercapto)-OH
CAS Number
2002-22-4
Purity
≥ 98% (TLC)
Molecular Formula
C6H9N3O2S
Molecular Weight
187.2
MDL Number
MFCD00047018
PubChem ID
3037745
Appearance
Slightly yellow powder
Optical Rotation
[a]D24 = -10 ± 2 º (C=1 in 1M HCl)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Mercapto-L-histidine is widely utilized in research focused on

  • Antioxidant Applications: This compound acts as a powerful antioxidant, helping to protect cells from oxidative stress. It's particularly valuable in the food industry to enhance the shelf life of products by preventing rancidity.
  • Pharmaceutical Development: It plays a crucial role in the formulation of drugs, especially in the development of treatments for conditions like cancer and neurodegenerative diseases, where it can help stabilize active pharmaceutical ingredients.
  • Biochemical Research: Researchers use it in studies related to enzyme activity and protein interactions, providing insights into cellular processes and potential therapeutic targets.
  • Metal Ion Chelation: The compound is effective in chelating metal ions, making it useful in environmental applications to remove heavy metals from contaminated water sources.
  • Cosmetic Formulations: Its antioxidant properties make it a valuable ingredient in skincare products, helping to protect the skin from damage caused by free radicals and promoting a healthier appearance.

Citations