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N-Acetyl-L-aspartic acid

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Identification
Molecular formula
C6H9NO5
CAS number
997-55-7
IUPAC name
4-acetamido-2-amino-butanoic acid
State
State

At room temperature, N-Acetyl-L-aspartic acid exists as a solid.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.15
Boiling point (Celsius)
720.00
Boiling point (Kelvin)
993.15
General information
Molecular weight
175.15g/mol
Molar mass
175.1750g/mol
Density
1.3590g/cm3
Appearence

N-Acetyl-L-aspartic acid is an off-white crystalline powder. It may appear slightly yellow depending on the purity and presence of impurities. It is typically odorless.

Comment on solubility

Solubility of 4-Acetamido-2-amino-butanoic acid (C6H9NO5)

4-Acetamido-2-amino-butanoic acid, often referred to as a derivative of amino acids, exhibits interesting solubility characteristics that are worth noting:

  • It is primarily soluble in water, benefiting from its polar functional groups which enhance interactions with water molecules.
  • The presence of the acetamido (-NH2) and carboxylic acid (-COOH) groups increases solubility due to hydrogen bonding capabilities.
  • It shows limited solubility in organic solvents, such as ethanol and acetone, which further emphasizes its polar nature.
  • Water solubility is often temperature dependent; as the temperature increases, solubility tends to improve, making it more accessible for various applications.

In summary, the solubility of 4-acetamido-2-amino-butanoic acid is characterized by its broad solubility in water and restricted solubility in organic solvents, reflecting the influence of its molecular structure on solvation dynamics.

Interesting facts

Interesting Facts about 4-Acetamido-2-Amino-Butanoic Acid

4-Acetamido-2-amino-butanoic acid, often abbreviated as AABA, is a fascinating compound with a variety of implications in both biochemistry and pharmaceutical applications. Here are some insightful details about this intriguing molecule:

  • Amino Acid Derivative: AABA is an important amino acid derivative, which contributes to numerous metabolic pathways in living organisms. Its structure allows it to act as a building block for proteins.
  • Therapeutic Potential: This compound has gained attention in research for its potential therapeutic uses, particularly in the modulation of neurological pathways, making it a candidate for drug development aimed at treating various neurological disorders.
  • Biological Importance: As an amino acid, it plays a crucial role in protein synthesis. Amino acids are the essential components for life, involved in numerous biological functions such as enzyme catalysis and immune responses.
  • Analytical Techniques: Scientists employ several analytical techniques to study this compound, including mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy, which help to elucidate its structure and behavior in different environments.
  • Structure-Activity Relationship (SAR): Understanding the structure of AABA helps researchers predict its biological activity, allowing for modifications that could yield more effective analogs for therapeutic uses.

As a compound with a blend of structural uniqueness and biological relevance, 4-acetamido-2-amino-butanoic acid continues to be an important subject of study in the fields of bioorganic chemistry and pharmaceutical science. Its diverse applications make it a vital focus for scientists looking to explore new avenues in drug discovery and biological research.

Synonyms
Butanoic acid, 4-(acetylamino)-2-amino-
4-acetamido-2-aminobutanoic acid
14531-48-7
DTXSID10274290
SCHEMBL1512848
Ng-Acetyl-L-diaminobutyric acid
DTXCID40225770
2-amino-4-acetylaminobutyric acid
CHEBI:188981