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Glutamine Aspartate

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Identification
Molecular formula
C9H17N3O6
CAS number
14834-58-9
IUPAC name
[(4S)-4-amino-4-carboxy-butyl]ammonium;(2S)-2-amino-4-hydroxy-4-oxo-butanoate
State
State

At room temperature, glutamine aspartate is in a solid state.

Melting point (Celsius)
177.50
Melting point (Kelvin)
450.70
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
287.24g/mol
Molar mass
287.2410g/mol
Density
1.6600g/cm3
Appearence

Glutamine aspartate typically appears as a white crystalline solid. It is often available in the form of a powder.

Comment on solubility

Solubility Observations

The compound [(4S)-4-amino-4-carboxy-butyl]ammonium;(2S)-2-amino-4-hydroxy-4-oxo-butanoate exhibits interesting solubility characteristics due to its unique structural features.


Solubility Characteristics

  • Polarity: This compound includes both amino and carboxy groups which can engage in hydrogen bonding. This often enhances solubility in polar solvents such as water.
  • Hydrophilicity: The presence of multiple functional groups (amino, carboxyl, and hydroxy) makes the compound highly hydrophilic. As a result, it is expected to dissolve readily in aqueous solutions.
  • Influencing Factors: Factors such as temperature, pH, and the presence of other ions can significantly influence its solubility. For example, at higher temperatures, solubility in water typically increases.
  • Comparison with Similar Compounds: When compared to other related compounds, the intricate balance of acidic and basic groups makes this compound soluble in various conditions.

In conclusion, the solubility of [(4S)-4-amino-4-carboxy-butyl]ammonium;(2S)-2-amino-4-hydroxy-4-oxo-butanoate can be considered substantial, primarily due to its functional groups that favor interactions with polar solvents. This type of solubility makes it particularly interesting for applications in biochemical contexts where solubility plays a crucial role!

Interesting facts

Discovering the Unique Compound: [(4S)-4-amino-4-carboxy-butyl]ammonium; (2S)-2-amino-4-hydroxy-4-oxo-butanoate

This intriguing compound embodies the fascinating world of biochemistry and amino acids. Here are some notable insights about it:

  • Amino Acids in Action: The compound combines features of amino acids and is closely linked to vital biological processes.
  • Chirality Matters: With its chiral centers, [(4S)-4-amino-4-carboxy-butyl]ammonium exhibits properties that may differ significantly from its mirror-image forms. This is a vital consideration in drug design, as chirality can influence a molecule's biological efficacy and safety.
  • Functional Groups: The presence of various functional groups, like amino, carboxylic acid, and hydroxyl groups, make it highly versatile and reactive, paving the way for diverse chemical interactions.
  • Biological Importance: Amino acids form the building blocks of proteins, and variations of these compounds play crucial roles in metabolic pathways and enzymatic functions.
  • Potential Therapeutic Uses: Research into compounds such as this one often opens doors to new therapeutic avenues, including their potential use in treating metabolic disorders or enhancing nutritional profiles.

This compound is more than just a combination of atoms; it holds the key to understanding complex biochemical processes and illustrates the intricate relationships within molecular structures that govern life itself. Chemistry students and scientists alike are continually drawn to study such compounds due to their theoretical implications and practical applications. As one researcher aptly said, "The beauty of chemistry lies in its ability to explain the very fabric of life."

Synonyms
Ornithylaspartate
UNII-JA08T3B97O
L-ornithinium(1+) (+)-aspartate
[(4S)-4-amino-4-carboxybutyl]azanium;(2S)-2-amino-4-hydroxy-4-oxobutanoate