Cystamine dihydrochloride
ADVERTISEMENT
- 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
Identification
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.