Cysteamine hydrochloride

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Identification

Molecular formula
C2H8ClNS
CAS Number
156-57-0
IUPAC Name
2-[(2R)-2-amino-2-carboxy-ethyl]sulfanylethylammonium;chloride
Molecular Weight
113.62g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
2-(Aminoethyl)cysteine monohydrochloride
Interesting facts

Interesting Facts about 2-[(2R)-2-amino-2-carboxy-ethyl]sulfanylethylammonium;chloride

This compound, commonly recognized in biochemical studies, possesses intriguing characteristics that make it significant within the field of chemistry and biochemistry. Known for its role as a *biochemical intermediate*, it participates in various metabolic processes.

Key Insights:

  • Structural Importance: The presence of the amino and carboxy groups illustrates the compound's potential as an amino acid derivative, contributing to its biological activity.
  • Biological Role: Compounds like this are often involved in the synthesis of proteins, playing crucial roles in cell metabolism and signaling.
  • Potential Applications:
    • As a precursor in drug development.
    • In research related to enzyme catalysis.
    • As a building block for more complex molecules.
  • Chloride Ion: The chloride anion contributes to the compound's solubility in water, which is essential for its functionality in biological systems.

Furthermore, scientists are exploring the therapeutic applications of similar compounds in treating various diseases, enhancing their potential in pharmacology. As the study of chemical compounds continues to expand, the understanding of 2-[(2R)-2-amino-2-carboxy-ethyl]sulfanylethylammonium;chloride could lead to breakthroughs in both medicine and biochemistry.

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