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Nitrosoproline

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Identification
Molecular formula
C5H9N2O4
CAS number
6004-66-4
IUPAC name
2-amino-5-(hydroxyamino)-5-oxo-pentanoic acid
State
State

At room temperature, Nitrosoproline is generally found in the solid state.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
160.14g/mol
Molar mass
160.1390g/mol
Density
1.4600g/cm3
Appearence

Nitrosoproline typically appears as a colorless solid. It may be crystalline in nature, depending on its form and method of purification.

Comment on solubility

Solubility of 2-amino-5-(hydroxyamino)-5-oxo-pentanoic acid

The solubility profile of 2-amino-5-(hydroxyamino)-5-oxo-pentanoic acid, with the chemical formula C5H9N2O4, reflects its distinctive structural characteristics. This compound features multiple functional groups which significantly affect its solubility in different solvents.

Key Factors Affecting Solubility:

  • Polarity: Due to the presence of amino and hydroxyl groups, this compound exhibits polar characteristics, making it more soluble in polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds contributes to its solubility in water, as these interactions stabilize the compound in solution.
  • pH Sensitivity: Being an amino acid derivative, the solubility can vary with changes in pH, affecting ionization and solvation.

In general, 2-amino-5-(hydroxyamino)-5-oxo-pentanoic acid is expected to be soluble in aqueous solutions, particularly when compared to non-polar organic solvents. Its solubility can be advantageous in biochemical applications, facilitating interactions in biological systems and making it accessible for various experimental procedures.

In summary, the solubility of this compound largely hinges on its polar nature and ability to engage in hydrogen bonding, making it a versatile choice in aqueous environments.

Interesting facts

Fascinating Insights into 2-Amino-5-(Hydroxyamino)-5-Oxo-Pentanoic Acid

2-Amino-5-(hydroxyamino)-5-oxo-pentanoic acid, also known as AHAP, is an intriguing compound with several noteworthy features:

  • Biological Significance: This compound is a derivative of aspartic acid and plays a role in biological systems, particularly in amino acid metabolism. Its structure contains a functional group that can potentially participate in enzyme catalysis and metabolism.
  • Entry into Metabolic Pathways: AHAP can be involved in the biosynthesis of important biomolecules, potentially influencing a range of physiological functions from neurotransmission to muscle contraction.
  • Research Applications: The unique structure of AHAP allows scientists to explore its use in drug development. Its properties could lead to novel therapeutic applications, particularly in the realms of neurology and metabolic disorders.
  • Synthesis Interest: Researchers are continually investigating efficient methods for synthesizing this compound. Mastery of such syntheses is critical for both academic research and pharmaceutical applications.

Quotes from researchers emphasize its potential: "Compounds like AHAP can unlock new pathways in metabolic research, offering insights into how we understand enzymes and co-factors."

In summary, 2-amino-5-(hydroxyamino)-5-oxo-pentanoic acid serves as a compelling subject of study in both organic chemistry and biochemistry. Its potential applications are exciting for students and professionals alike, paving the way for future innovations!

Synonyms
1955-67-5
L-Glutamic acid gamma-monohydroxamate
AMINO ACID HYDROXAMATES L-GLUTAMIC ACID GAMMA-MONOHYDROXAMATE
2-amino-5-(hydroxyamino)-5-oxopentanoic acid
SCHEMBL7645305
L-Glutamic gamma-monohydroxamate
L-Glutamic acid ?-monohydroxamate
BAA95567