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Glutamylalanine

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Identification
Molecular formula
C10H18N2O5
CAS number
39536-76-8
IUPAC name
5-amino-2-(3-carboxypropanoylamino)pentanoic acid
State
State

At room temperature, Glutamylalanine is in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
247.26g/mol
Molar mass
247.2570g/mol
Density
1.4600g/cm3
Appearence

Glutamylalanine is typically a white crystalline powder. The appearance can vary based on purity and form, but it generally lacks color and has a crystalline structure.

Comment on solubility

Solubility of 5-amino-2-(3-carboxypropanoylamino)pentanoic acid

This intriguing compound, 5-amino-2-(3-carboxypropanoylamino)pentanoic acid (C10H18N2O5), exhibits unique solubility properties primarily due to its **amino** and **carboxylic acid** functional groups. These functional groups enhance its interaction with water molecules, resulting in significant solubility under certain conditions. Here are some key points regarding its solubility:

  • Hydrophilic Nature: The presence of multiple carboxylic acid groups contributes to the compound's high polarity, allowing it to dissolve well in polar solvents like water.
  • pH Dependency: The solubility may vary with the pH of the solution; at physiological pH, it is likely to be more soluble due to the ionization of the carboxyl groups.
  • Temperature Effect: Increased temperatures generally enhance solubility for many organic compounds, which might also apply to this particular acid under certain circumstances.
  • Solvent Choice: While water is a primary solvent for this compound, its solubility might be reduced in non-polar solvents, emphasizing the importance of solvent selection in practical applications.

In summary, **5-amino-2-(3-carboxypropanoylamino)pentanoic acid** exhibits good solubility in water, largely driven by its polar functional groups. Understanding its solubility characteristics is crucial for applications in biochemistry and pharmaceuticals.

Interesting facts

Exploring 5-Amino-2-(3-carboxypropanoylamino)pentanoic Acid

5-Amino-2-(3-carboxypropanoylamino)pentanoic acid is an intriguing compound that showcases the beauty of organic chemistry and its applications in various fields. This compound, boasting a complex structure, serves as a valuable model in the study of amino acid derivatives and peptide synthesis.

Key Features

  • Amino Acid Derivative: This compound is an important amino acid derivative that has connections to protein synthesis and metabolic pathways.
  • Biological Relevance: It can play a role in various biological processes, including enzyme functions and cellular metabolism.
  • Synthetic Applications: Chemists often explore this compound for its potential use in the synthesis of more complex biomolecules and pharmaceuticals.
  • Environmental Impact: Studying such compounds can help in understanding their impact on ecological systems, particularly in relation to nutrient cycles.

One of the fascinating aspects of 5-amino-2-(3-carboxypropanoylamino)pentanoic acid is its structural complexity, which illustrates how slight modifications to amino acids can lead to significant changes in properties and functionalities. Researchers often say, "In the world of chemistry, even a small change can lead to fascinating new worlds of possibility." This highlights the exploration in molecular design and its implications across various fields, including pharmacology and agrochemicals.

This compound represents a small yet significant piece of the vast puzzle of biochemistry. As we continue to unlock the mysteries of such remarkable substances, we pave the way for breakthroughs in drug development, environmental science, and bioengineering.

Synonyms
899816-95-6
N~2~-(3-Carboxypropanoyl)ornithine
5-AMINO-2-(3-CARBOXYPROPANOYLAMINO)PENTANOIC ACID
DTXSID70274291