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Proline Cysteine Mix

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Identification
Molecular formula
C9H14N2O4S
CAS number
null
IUPAC name
1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid
State
State
This compound is typically solid at room temperature, characterized by its crystalline form and stable configuration.
Melting point (Celsius)
152.50
Melting point (Kelvin)
425.60
Boiling point (Celsius)
275.80
Boiling point (Kelvin)
548.80
General information
Molecular weight
246.31g/mol
Molar mass
246.3100g/mol
Density
1.3000g/cm3
Appearence

The compound appears as a crystalline solid, usually white to off-white in color. Its granular structure is visibly distinct under magnification.

Comment on solubility

Solubility of 1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid

The solubility of 1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid (C9H14N2O4S) can be quite intriguing due to its structural characteristics. This compound contains functional groups that can influence its behavior in solvents.

Key factors affecting its solubility include:

  • Polarity: The presence of carboxylic acid groups generally increases solubility in polar solvents such as water due to hydrogen bonding.
  • Hydrophobic regions: The aliphatic and nitroso components may impart hydrophobic characteristics, potentially reducing solubility in aqueous environments.
  • Interactions with solvents: This compound may exhibit unique interactions in certain organic solvents, promoting solubility in those specific mediums not present in polar solvents.

It is important to note that, as with many compounds, solubility can also be influenced by several external factors, including:

  • Temperature: Increased temperature typically enhances solubility.
  • pH of the solution: The ionization state of the carboxylic acid group can shift depending on the pH, further influencing solubility.
  • Concentration: Higher concentrations may lead to saturation, impacting solubility dynamics.

In conclusion, while the overall solubility of this compound may vary, it likely favors polar solvents owing to its functional groups, while also showing variable solubility in nonpolar solvents, making it a subject of fascinating study.

Interesting facts

Interesting Facts about 1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid

1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid is a compound that offers a fascinating glimpse into the complex realm of organic chemistry, particularly due to its unique structural features and potential biological activities.

Structural Highlights

  • Nitrosothiol Formation: This compound contains a nitrosothiol functional group, which is significant as it can participate in various biochemical processes, including signaling mechanisms in biological systems.
  • Pyrrolidine Ring: The presence of a pyrrolidine ring is noteworthy, as such cyclic amines often exhibit diverse pharmacological properties.
  • Amino Acid Derivative: As a derivative of an amino acid, it sheds light on modifications that can enhance biological activity or alter pharmacokinetics.

Applications and Potential Uses

This compound may have valuable applications in medicinal chemistry due to its structural analogies with biologically relevant molecules. Here are some potential areas of interest in research:

  • Drug Development: Investigating its role in drug compounds could lead to the discovery of new therapeutic agents.
  • Biochemical Research: Exploring its behavior can help understand redox reactions and signaling pathways influenced by nitrosothiols.
  • Agrochemicals: Similar structures have been explored for their efficacy in agricultural applications, possibly serving as novel pesticides or herbicides.

Conclusion

The intriguing interplay of functional groups and cyclic structures in 1-(2-methyl-3-nitrososulfanyl-propanoyl)pyrrolidine-2-carboxylic acid makes it a compound worthy of investigation. As scientists continue to unravel the complexities of such compounds, they pave the way for breakthroughs in various fields, from pharmacology to agriculture.