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N-Acetylaspartic acid

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Identification
Molecular formula
C6H9NO5
CAS number
997-55-7
IUPAC name
2-amino-4-(3-carboxypropanoyloxy)butanoic acid
State
State

At room temperature, N-Acetylaspartic acid is typically observed as a solid.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.00
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.00
General information
Molecular weight
175.15g/mol
Molar mass
175.1500g/mol
Density
1.1829g/cm3
Appearence

N-Acetylaspartic acid appears as a white crystalline solid. It is generally found in its pure form in laboratories.

Comment on solubility

Solubility of 2-amino-4-(3-carboxypropanoyloxy)butanoic acid

2-amino-4-(3-carboxypropanoyloxy)butanoic acid, with the chemical formula C6H9NO5, is a complex organic compound known for its unique solubility characteristics.

This compound exhibits variable solubility in different solvents, which can be summarized as follows:

  • Water: Generally, this compound is soluble in water due to its multiple functional groups capable of forming hydrogen bonds with water molecules.
  • Alcohols: It often shows good solubility in alcohols, particularly in lower alcohols like methanol and ethanol, which can stabilize its polar groups.
  • Non-polar solvents: 2-amino-4-(3-carboxypropanoyloxy)butanoic acid tends to be insoluble in non-polar solvents such as hexane and toluene due to its polar nature.

Furthermore, temperature and pH can significantly influence its solubility:

  • Temperature: As with many compounds, increasing the temperature generally increases solubility in aqueous solutions.
  • pH levels: The solubility behavior may change depending on the protonation state of the amino and carboxyl groups, highlighting the importance of pH in solution chemistry.

In conclusion, the solubility profile of 2-amino-4-(3-carboxypropanoyloxy)butanoic acid makes it a fascinating subject for further research, particularly in biochemistry and pharmaceuticals where solubility plays a critical role.

Interesting facts

Interesting Facts about 2-amino-4-(3-carboxypropanoyloxy)butanoic acid

2-amino-4-(3-carboxypropanoyloxy)butanoic acid, commonly recognized for its role in various biological systems, is a fascinating compound worth exploring. Here are some compelling aspects:

  • Biological Significance: This compound plays a critical role as a building block for biosynthesis, closely related to amino acids that are vital for protein structure and function.
  • Functionality: It contains both amino and carboxylic acid functional groups, allowing it to participate in a range of chemical reactions. This dual functionality makes it a versatile molecule in biochemical processes.
  • Metabolic Pathways: Being involved in metabolic pathways, this compound contributes to essential biochemical reactions, which are fundamental for maintaining homeostasis within living organisms.
  • Research Applications: In scientific research, compounds like 2-amino-4-(3-carboxypropanoyloxy)butanoic acid are studied for their potential applications in pharmaceuticals and therapeutic developments. Their biochemical properties can lead to novel treatments for various diseases.
  • Synthetic Utility: Chemists often explore the synthesis of this molecule because of its complex structure, which provides valuable insights into organic synthesis techniques and methodologies.

In conclusion, the diversity and significance of 2-amino-4-(3-carboxypropanoyloxy)butanoic acid make it an intriguing subject of study in the fields of chemistry and biology. As it bridges the gap between biological functions and synthetic applications, it stands out as a compound rich in potential discoveries.

Synonyms
Homoserine, O-succinyl-
o-(3-carboxypropanoyl)homoserine
SCHEMBL2263158
CHEBI:181442
GNISQJGXJIDKDJ-UHFFFAOYSA-N
2-amino-4-(3-carboxypropanoyloxy)butanoic acid
E1C5F2CF-F34A-4086-86BB-2132D5EB99B9
1817-00-1