Cystamine dihydrochloride

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Identification

Molecular formula
C4H12N2S2Cl2
CAS Number
56-17-7
IUPAC Name
2-(phenyldisulfanyl)ethylammonium;chloride
Molecular Weight
221.71g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4090g/cm3
Synonyms
2-(Phenyldithio)ethylamine hydrochloride
Interesting facts

Interesting Facts about 2-(phenyldisulfanyl)ethylammonium Chloride

2-(phenyldisulfanyl)ethylammonium chloride is a fascinating compound with a unique combination of features that make it a subject of interest within the field of chemistry. Here are some intriguing points regarding this compound:

  • Structural Complexity: The presence of a phenyldisulfanyl group in its structure adds significant complexity, making it an interesting example of organosulfur compounds.
  • Applications: Compounds like 2-(phenyldisulfanyl)ethylammonium chloride are often studied for their potential antimicrobial properties, showcasing the importance of organosulfur chemistry in pharmaceutical development.
  • Biological Activity: The disulfide linkage can play a crucial role in biological systems, influencing the reactivity and stability of the compound, particularly in the presence of thiols.
  • Synthesis Relevance: Understanding the synthesis of this compound provides valuable insights into the techniques used for creating disulfide compounds, which are important in medicinal chemistry.
  • Ion Exchange Properties: As a quaternary ammonium salt, 2-(phenyldisulfanyl)ethylammonium chloride may exhibit unique ion exchange properties, making it useful in various chemically specific applications.

In summary, 2-(phenyldisulfanyl)ethylammonium chloride is not just another amine salt; its interesting structural features and potential applications make it a noteworthy compound in the realm of chemical research.

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