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N-Acetyl-L-glutamic acid

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

The compound is solid at room temperature, reflecting its crystalline form.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
580.00
Boiling point (Kelvin)
853.15
General information
Molecular weight
189.19g/mol
Molar mass
189.1860g/mol
Density
1.3850g/cm3
Appearence

N-Acetyl-L-glutamic acid appears as a white crystalline powder. This compound is typically solid at room temperature.

Comment on solubility

Solubility of 2-acetamido-5-amino-5-oxo-pentanoic acid

2-acetamido-5-amino-5-oxo-pentanoic acid, a compound that exhibits intriguing solubility properties, is known to be quite soluble in a variety of solvents. Here are some key points regarding its solubility:

  • Water Solubility: This compound is readily soluble in water due to its polar functional groups, which facilitate interactions with water molecules.
  • Solvent Interactions: Besides water, it is also soluble in organic solvents such as methanol and ethanol, owing to its versatile chemical structure.
  • pH Dependence: The solubility can be influenced by the pH of the solution, as variations can lead to protonation or deprotonation of the amino and carboxyl groups.
  • Temperature Effects: Increasing the temperature generally enhances solubility, aligning with the common trend observed in many organic compounds.

As with many amino acids and their derivatives, the degree of solubility can vary based on concentration and the chemical environment. In essence, 2-acetamido-5-amino-5-oxo-pentanoic acid's solubility characteristics make it a compound of interest for various biochemical applications.

Interesting facts

Interesting Facts about 2-Acetamido-5-amino-5-oxo-pentanoic acid

2-Acetamido-5-amino-5-oxo-pentanoic acid, often referred to as a derivative of aspartic acid, is a notable compound in the field of biochemistry due to its structural features and potential applications.

Key Features of 2-Acetamido-5-amino-5-oxo-pentanoic acid

  • Structural Significance: This compound contains an amido group as well as an amino group, making it a vital intermediate in various biological processes.
  • Biochemical Relevance: It plays a significant role in the synthesis of important biomolecules and can serve as a precursor in nitrogen metabolism.
  • Potential Applications: Due to its unique structure, researchers are exploring its utility in pharmaceutical developments, particularly in relation to amino acid metabolism and related disorders.

Moreover, the presence of both acetamido and oxo functionalities within its structure emphasizes its versatility in chemical reactions. As a compound of interest, it not only helps in understanding amino acid transformations but could also pave the way for new synthetic pathways in organic chemistry.

Interesting Tidbit:

In the words of renowned chemists, “The beauty of chemistry is in the connections we make not just with our reactions, but with the compounds that are essential for life itself.” This compound exemplifies that beauty by bridging the gap between simple amino acids and complex biological functions.

Overall, 2-acetamido-5-amino-5-oxo-pentanoic acid offers exciting possibilities for research and application, making it a compelling subject of study for chemists and biochemists alike.

Synonyms
4-carbamoyl-2-acetamidobutanoic acid
5817-09-4
825-602-8
Acetylglutamine
2-acetamido-5-amino-5-oxopentanoic acid
N(2)-acetylglutamine
CHEBI:73685
Glutamine, N2-acetyl-, L- (8CI)
Ac-D-Gln-OH
Glutamine, N-acetyl-
alpha-N-Acetyl-L-glutamine;N2-Acetylglutamine
N-alpha-Acetyl-L-glutamine
Acetyl-D-glutamine
NCGC00183120-01
bmse000145
bmse001000
SCHEMBL287577
ALPHA-N-ACETYL-GLUTAMINE
CHEMBL3184604
HMS5083L03
4-carbamoyl-2-acetamidobutanoicacid
MFCD00867899
MSK169997
SBB067153
AKOS000159972
AKOS016605458
2-(acetylamino)-4-carbamoylbutanoic acid
SY057113
SY353364
DB-046574
2-(acetylamino)-5-amino-5-oxopentanoic acid
EN300-65857
Q4673064
Z85900147
10B6E98F-2CB8-4D96-80D6-1CDC5541D3B2