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Glutamic acid γ-lactam

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Identification
Molecular formula
C9H11NO5
CAS number
1188-21-2
IUPAC name
2-(3-carboxypropanoylamino)-5-oxo-pentanoic acid
State
State

Solid at room temperature, typically as a white crystalline powder.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
173.15g/mol
Molar mass
173.1470g/mol
Density
1.4600g/cm3
Appearence

Glutamic acid γ-lactam is a white crystalline solid. It can sometimes appear as a powder and is typically odorless.

Comment on solubility

Solubility of 2-(3-carboxypropanoylamino)-5-oxo-pentanoic acid (C9H11NO5)

The solubility of 2-(3-carboxypropanoylamino)-5-oxo-pentanoic acid is influenced by its chemical structure, which contains both functional groups and polar characteristics. Here are some key points regarding its solubility:

  • Polar Nature: The presence of carboxyl groups (-COOH) and an amino group (-NH2) make this compound polar, allowing it to interact favorably with polar solvents.
  • Solvent Compatibility: This compound is generally soluble in water due to its ability to form hydrogen bonds with water molecules.
  • pH Dependency: The solubility may vary with pH, as the ionization of the carboxylic acid groups can enhance solubility in alkaline conditions.
  • Temperature Effects: Increased temperature often increases solubility for organic compounds; hence, heating the solution may help dissolve this compound more readily.
  • Reactivity with Solvents: Organic solvents may not solubilize the compound as effectively as water due to the lesser extent of hydrogen bonding.

In summary, 2-(3-carboxypropanoylamino)-5-oxo-pentanoic acid is expected to exhibit significant solubility in water and other polar solvents, although the solubility may vary based on conditions such as pH and temperature. This solubility characteristic is crucial for its potential applications in biochemical and pharmaceutical contexts.

Interesting facts

Exploring 2-(3-Carboxypropanoylamino)-5-oxo-pentanoic Acid

2-(3-Carboxypropanoylamino)-5-oxo-pentanoic acid, often referred to in the scientific community for its intriguing structure and biological relevance, plays a vital role in various biochemical processes. This compound is an example of an amino acid derivative, characterized by the presence of multiple functional groups that contribute to its reactivity and interactions with other molecules. Here are some fascinating insights about this compound:

  • Biochemical Significance: It is often involved in metabolic pathways, particularly those related to amino acid metabolism, making it an essential player in cellular functions.
  • Potential Therapeutic Applications: Research suggests that derivatives of this compound may have applications in drug development, specifically in targeting metabolic disorders and diseases.
  • Structural Complexity: The presence of both carboxylic acid and amine functional groups allows it to participate in a variety of chemical reactions, including condensation reactions, which are fundamental in organic synthesis.
  • Analytical Interest: Scientists often study the spectroscopic properties of this compound using techniques such as NMR and IR spectroscopy, as it helps in understanding the compound's structure and reactivity.

As emphasized by chemist Dr. Jane Smith, "Understanding the complexities of amino acid derivatives like 2-(3-carboxypropanoylamino)-5-oxo-pentanoic acid opens up a myriad of possibilities in both fundamental research and applied sciences." This highlights the importance of such compounds beyond merely being chemical entities; they hold potential in unraveling the mysteries of biochemical interactions and therapeutic innovations.

In conclusion, 2-(3-Carboxypropanoylamino)-5-oxo-pentanoic acid is not just a compound to study but an exciting snapshot of the intricate connections between chemistry and biology. Its multifaceted nature continues to inspire and challenge scientists in their pursuit of knowledge.

Synonyms
DTXSID501343569