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S-Sulfocysteine

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Identification
Molecular formula
C3H6NO5S2Na
CAS number
15042-96-9
IUPAC name
sodium;(2R)-2-amino-3-sulfosulfanyl-propanoate
State
State

At room temperature, S-Sulfocysteine exists in a solid state. The compound's ionic nature, due to its sulfonate group, typically implies it forms a type of salt, specifically a sodium salt in this case, which contributes to its solid-state form.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
239.20g/mol
Molar mass
0.0000g/mol
Density
2.2313g/cm3
Appearence

S-Sulfocysteine typically appears as a crystalline solid. Due to the ionic nature of its sulfate group, it is often found in a hydrated form, which can affect its crystalline appearance. It is colorless to white in form.

Comment on solubility

Solubility of Sodium (2R)-2-Amino-3-sulfosulfanyl-propanoate

Sodium (2R)-2-amino-3-sulfosulfanyl-propanoate, commonly referred to in the context of sulfonic acid derivatives, exhibits interesting solubility characteristics that are worth noting. This compound's structure, containing both amino and sulfonic acid groups, greatly influences its solubility in various solvents.

Key solubility attributes include:

  • High water solubility: Due to the presence of the sulfonic acid group, the compound is expected to be highly soluble in polar solvents, particularly water.
  • Influence of pH: The solubility can vary with pH levels, as the protonation status of the amino and sulfonic groups affects the compound's ionic character.
  • Temperature dependence: Like many ionic compounds, solubility may increase with temperature, making the dissolution process more efficient.
  • Interactions with other solutes: The presence of other ionic species in a solution could lead to either increased solubility due to cosolvency or decreased solubility via ion pairing.

As a rule of thumb, compounds like sodium (2R)-2-amino-3-sulfosulfanyl-propanoate are often more soluble in aqueous environments compared to organic solvents due to their ionic nature. Therefore, the solubility of such compounds is a critical factor in applications ranging from biochemical research to pharmaceutical formulations.

Interesting facts

Interesting Facts about Sodium (2R)-2-amino-3-sulfosulfanyl-propanoate

Sodium (2R)-2-amino-3-sulfosulfanyl-propanoate, commonly referred to as a sulfonic acid derivative, is a compound of significant interest in various fields, including biochemistry and pharmaceutical research.

Key Characteristics

  • Biological Relevance: This compound serves as a precursor for the synthesis of amino acids and could play a role in metabolic pathways.
  • Research Application: It is being explored for its potential therapeutic applications, especially in the treatment of metabolic disorders.
  • Unique Functional Group: The sulfonyl group in its structure increases its water solubility and potential reactivity, making it a versatile compound in chemical reactions.

One of the fascinating aspects of sodium (2R)-2-amino-3-sulfosulfanyl-propanoate is its chirality. Being a chiral molecule, it exists in two enantiomeric forms, which can have different biological activities and properties. As highlighted by researchers, "the specificity of enantiomers can lead to varied interactions in biological systems, highlighting the importance of stereochemistry in pharmacology."

Potential Applications

  • As an intermediate in the synthesis of more complex bioactive compounds.
  • In diagnostics, particularly in the development of assays for amino acid detection.
  • In biochemical studies, to explore metabolic pathways involving sulfurs and their derivatives.

In summary, sodium (2R)-2-amino-3-sulfosulfanyl-propanoate is much more than just a simple chemical compound. Its unique properties and potential applications in science and medicine make it a compound worth studying and understanding.