Skip to main content

N-Acetyl-L-glutamic acid

ADVERTISEMENT
Identification
Molecular formula
C7H11NO5
CAS number
1188-37-0
IUPAC name
2-acetamido-5-oxo-pentanoic acid
State
State

At room temperature, N-Acetyl-L-glutamic acid is a solid.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.00
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.00
General information
Molecular weight
189.18g/mol
Molar mass
189.1760g/mol
Density
1.4770g/cm3
Appearence

N-Acetyl-L-glutamic acid appears as a white crystalline solid.

Comment on solubility

Solubility of 2-acetamido-5-oxo-pentanoic acid (C7H11NO5)

2-acetamido-5-oxo-pentanoic acid is a fascinating compound with a unique solubility profile. Its solubility can be influenced by several factors, making it an interesting subject of study. Here are some key points regarding its solubility:

  • Polar Nature: The presence of polar functional groups, such as the acetamido and carboxylic acid moieties, contributes to the overall polar character of this compound.
  • Water Solubility: It is generally expected that compounds like C7H11NO5 exhibit good solubility in water due to their hydrogen bonding capabilities. This can help facilitate dissolution in aqueous environments.
  • Organic Solvents: Depending on the specific structure and interactions, the solubility may vary in organic solvents. Factors such as the presence of polar vs. nonpolar solvents are critical for understanding its behavior.
  • pH Influence: The solubility of acids can be affected by pH levels, especially since C7H11NO5 contains a carboxylic acid group, which may ionize in alkaline conditions, potentially increasing solubility.

In conclusion, the solubility of 2-acetamido-5-oxo-pentanoic acid is largely governed by its polar structure, interactions with solvents, and environmental conditions such as pH. Understanding these aspects is crucial for applications in pharmaceuticals, biochemistry, and related fields.

Interesting facts

Interesting Facts about 2-Acetamido-5-Oxo-Pentanoic Acid

2-Acetamido-5-oxo-pentanoic acid is a fascinating compound with several intriguing aspects that make it relevant in the field of chemistry and biochemistry. Here are some noteworthy facts:

  • Biological Role: This compound plays a significant role as a metabolic intermediate in various biological processes. It is integral to the biosynthesis of amino acids and can be involved in the synthesis of important biomolecules.
  • Amide Functionality: The presence of the acetamido group (–NHCOCH3) lends unique properties to this compound. Amides are known for their relatively high stability, which makes compounds like this valuable in pharmaceutical applications.
  • Research Significance: Compounds containing the oxo group (–C=O) are often studied in drug design, as they can enhance the biological activity of certain pharmacologically active compounds.
  • Chemical Versatility: Due to its structure, 2-acetamido-5-oxo-pentanoic acid can undergo various chemical reactions, such as esterification and amidation, providing a rich platform for synthetic chemistry and drug development.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This sentiment resonated with the approach scientists take when exploring the potential applications of compounds like 2-acetamido-5-oxo-pentanoic acid.

With its intriguing molecular architecture and multifaceted applications, this compound continues to pique the interest of researchers and students alike, serving as a gateway to explore the intricate connections between chemistry and biology.

Synonyms
SCHEMBL11574620