Skip to main content

Cysteamine S-sulfate

ADVERTISEMENT
Identification
Molecular formula
C6H15NO3S2
CAS number
4444-14-2
IUPAC name
1-amino-6-sulfosulfanyl-hexane
State
State

At room temperature, cysteamine S-sulfate is typically found in a solid state.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.00
Boiling point (Celsius)
329.85
Boiling point (Kelvin)
603.00
General information
Molecular weight
187.30g/mol
Molar mass
187.3010g/mol
Density
1.4006g/cm3
Appearence

Cysteamine S-sulfate typically appears as a white crystalline powder. It is susceptible to absorbing moisture from the air, so it may appear slightly damp if not stored properly.

Comment on solubility

Solubility of 1-amino-6-sulfosulfanyl-hexane

The solubility of 1-amino-6-sulfosulfanyl-hexane can be influenced by various factors such as polarity, the presence of functional groups, and solvent interactions. Here are some key points to consider:

  • Polarity: This compound contains both amino and sulfonyl groups, which are likely to contribute to its overall polarity.
  • Hydrophilicity: The presence of the sulfonyl group suggests that 1-amino-6-sulfosulfanyl-hexane may be highly soluble in water, as sulfonic acids are known to impart water solubility to organic compounds.
  • Solvent interactions: Depending on the solvent, the solubility can vary significantly. In polar solvents, one might observe increased solubility compared to non-polar solvents.
  • Concentration effects: At higher concentrations, even compounds that are generally soluble can exhibit reduced solubility due to saturation.

In summary, the solubility of 1-amino-6-sulfosulfanyl-hexane is expected to be strong in polar solvents like water due to its molecular structure, but specific solubility values would require empirical testing. Proper consideration of these attributes is crucial for understanding its behavior in different environments.

Interesting facts

Interesting Facts about 1-Amino-6-sulfosulfanyl-hexane

1-amino-6-sulfosulfanyl-hexane is a fascinating compound that showcases the complexity and versatility found within organic chemistry. Here are some intriguing points to consider:

  • Amine and Sulfanyl Groups: This compound features both an amino group and a sulfosulfanyl group, making it an excellent subject for studying the interplay between nitrogen-containing moieties and sulfur-containing functionalities.
  • Biochemical Significance: Compounds with similar structures are often found in biological systems, where they may play roles in various enzymatic processes, signaling pathways, or even as potential pharmaceuticals.
  • Synthesizing Innovation: The process of synthesizing this compound can lead to valuable skills and techniques in organic chemistry, particularly in the realm of *nucleophilic substitutions* and *functional group interconversions*.
  • Applications in Research: Due to its unique structure, 1-amino-6-sulfosulfanyl-hexane may be investigated for applications in drug development, materials science, or as a part of *surfactants* in industrial applications.
  • Potential Toxicology Studies: Studying the effects and safety of this compound can contribute to understanding its behavior in living organisms, paving the way for future toxicology and safety assessments.

Moreover, *interdisciplinary approaches* combining chemistry, biology, and materials science could reveal new insights surrounding this compound. As researchers delve deeper, they often find that such unique compounds can lead to *unexpected discoveries* and *innovative applications* in various fields.

In the words of chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” Exploring compounds like 1-amino-6-sulfosulfanyl-hexane can certainly generate a wealth of ideas for scientists striving for innovation!

Synonyms
21679-18-5
1-HEXANETHIOL, 6-AMINO-, HYDROGEN SULFATE (ester)
DTXSID10176063
BRN 1773493
Thiosulfuric acid, 6-aminohexyl ester
RefChem:1100042
DTXCID0098554
SCHEMBL14910790
4-04-00-01787 (Beilstein Handbook Reference)
Thiosulfuric acid (H2S2O3), S-(6-aminohexyl) ester