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Nitrosoglutathione

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Identification
Molecular formula
C3H7N3O4
CAS number
15940-15-5
IUPAC name
(2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid
State
State

At room temperature, Nitrosoglutathione is typically in a solid state, appearing as a crystalline powder. It is stable under regular environmental conditions but should be stored away from light and moisture to maintain its properties.

Melting point (Celsius)
259.00
Melting point (Kelvin)
532.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
178.16g/mol
Molar mass
178.1560g/mol
Density
1.7500g/cm3
Appearence

Nitrosoglutathione is typically a white crystalline powder. It is known for its unique ability to convey nitroso and glutathione groups, each playing significant roles in various biochemical processes.

Comment on solubility

Solubility of (2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid

The solubility of (2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid, also known as a derivative of an amino acid, is influenced by its unique chemical structure.

  • Polar Nature: Due to the presence of both amino and hydroxy groups in the molecule, it exhibits significant polarity, which generally enhances solubility in polar solvents like water.
  • Functional Groups: The hydroxyl and nitroso functionalities can interact favorably with water through hydrogen bonding, which is crucial for solubility.
  • pH Sensitivity: The solubility might vary with pH changes as it can exist in different ionic states, which can affect its ability to dissolve.

In light of these factors, it can be concluded that (2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid is likely to be quite soluble in aqueous solutions. However, it is important to note that empirical testing is necessary for precise solubility data, as interactions with different solvents and conditions can yield varying results.

Interesting facts

Interesting Facts about (2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid

(2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid, often referred to in scientific circles due to its intriguing structure and potential applications, is noteworthy for several reasons:

  • Nitroso Group Significance: The incorporation of a nitroso group in its structure suggests potential for unique reactivity and biological interactions, making it an interesting subject of study in biochemistry.
  • Role in Metabolism: This compound, related to amino acids, may participate in metabolic pathways that are crucial for cellular function and health, particularly in the synthesis of proteins and other biomolecules.
  • Possible Therapeutic Applications: Given its structure, researchers are investigating its potential as a therapeutic agent, particularly in the modulation of nitric oxide levels which are essential for various physiological processes.
  • Chirality: The "(2S)" designation indicates that this compound has chirality, which can lead to different biological activities between its enantiomers, underlining the importance of stereochemistry in pharmacology.

The compound's complex interactions in biological systems and its unique characteristics make it a fascinating topic for further exploration in both academic and pharmaceutical chemistry. As we continue to study such compounds, we unravel the intricate layers of biochemistry and the fascinating capabilities inherent in molecular structures.

In the words of scientists exploring this compound:

“Understanding the subtleties of amino acid derivatives opens new doors in therapeutic development.”

Stay tuned as research advances, and breakthroughs may emerge from the study of compounds like (2S)-2-amino-3-[hydroxy(nitroso)amino]propanoic acid!