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N-Acetyl-L-aspartic acid

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Identification
Molecular formula
C8H11NO6
CAS number
997-55-7
IUPAC name
2-(3-carboxypropanoylamino)pentanedioic acid
State
State

At room temperature, N-Acetyl-L-aspartic acid is in a solid state. It is stable and does not decompose at the standard room conditions.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
189.17g/mol
Molar mass
189.1660g/mol
Density
1.3350g/cm3
Appearence

This compound is typically a solid at room temperature. It is a white, crystalline substance with a mild characteristic odor.

Comment on solubility

Solubility of 2-(3-carboxypropanoylamino)pentanedioic acid (C8H11NO6)

2-(3-carboxypropanoylamino)pentanedioic acid, also known as a complex amino acid derivative, exhibits intriguing solubility characteristics that are influenced by its molecular structure. Understanding the solubility of this compound can provide important insights into its potential applications and behaviors in various environments.

Key Points About Solubility:

  • This compound is expected to be soluble in water due to the presence of multiple carboxylic acid groups, which enhance its polarity.
  • The presence of polar functional groups allows for hydrogen bonding with water molecules, promoting solubility.
  • As an amino acid derivative, it may also exhibit amphoteric behavior; thus, its solubility might vary with pH changes.
  • It may form salts with bases, potentially increasing its solubility in basic solutions.

In summary, the solubility of 2-(3-carboxypropanoylamino)pentanedioic acid is primarily influenced by its hydrophilic functional groups. As a result:

  • In neutral pH environments, it is likely to exhibit significant solubility.
  • In acidic or basic conditions, its solubility may either increase or decrease based on the ionization of its functional groups.

Overall, understanding the solubility of this compound is crucial for its utilization in formulations and reactions, reinforcing the idea that solubility plays a pivotal role in the practical applications of chemical compounds.

Interesting facts

Exploring 2-(3-Carboxypropanoylamino)pentanedioic Acid

2-(3-Carboxypropanoylamino)pentanedioic acid is a fascinating compound in the realm of organic chemistry and biochemistry. Here are some compelling facts that showcase its significance:

  • Biological Relevance: This compound plays a crucial role in various metabolic pathways, primarily in amino acid metabolism and synthesis. Its unique structure potentially contributes to the functionality and regulation of enzymes involved in these pathways.
  • Structural Features: The presence of both carboxyl and amino groups in its structure allows it to participate in a range of biochemical reactions, enabling it to function as an intermediate in biosynthetic processes.
  • Potential Applications: Researchers are investigating the use of 2-(3-carboxypropanoylamino)pentanedioic acid in drug designs, particularly in developing therapies for metabolic disorders and diseases related to amino acid imbalances.
  • Synthesis Challenges: The synthesis of this compound can present challenges regarding selectivity and yield due to its complex structure. Understanding its synthesis opens doors to explore new methods in organic chemistry.
  • Research Interest: This compound has attracted attention for further research in fields such as pharmacology and nutrition. Its diverse functional groups make it a perfect candidate for studying molecular interactions.

As you dive deeper into the world of 2-(3-carboxypropanoylamino)pentanedioic acid, you'll discover how remarkable compounds like this can lead to breakthroughs in science and medicine.

Synonyms
SCHEMBL6270974
AKOS015970131