L-Alanyl-D-glutamic acid | Solubility of Things

Identification

Molecular formula

C₈H₁₅N₂O₄

CAS number

3383-45-9

IUPAC name

2-(1-carboxyethylamino)pentanoic acid

State

At room temperature, L-Alanyl-D-glutamic acid is found in a solid state, typically as a stable, non-hygroscopic white crystalline powder.

Melting point (Celsius)

234.00

Melting point (Kelvin)

507.15

Boiling point (Celsius)

-1.00

Boiling point (Kelvin)

-1.00

General information

Molecular weight

189.20g/mol

Molar mass

189.2040g/mol

Density

1.4095g/cm³

Appearence

L-Alanyl-D-glutamic acid appears as a white crystalline powder. It is typically odorless and has a slightly acidic taste. The crystals are not hygroscopic and are stable under standard conditions.

Comment on solubility

Solubility of 2-(1-carboxyethylamino)pentanoic acid

2-(1-carboxyethylamino)pentanoic acid, with the chemical formula C₈H₁₅N₂O₄, is known for its unique solubility characteristics, influenced by its amino acid structure.

Key Points on Solubility:

Aqueous Solubility: This compound is likely to be soluble in water due to the presence of both carboxylic acid and amino groups, which can engage in hydrogen bonding.
Temperature Dependence: Like many organic compounds, its solubility may vary with temperature; typically, higher temperatures can increase solubility.
Solvent Specificity: Solubility behavior may differ in non-polar solvents, where this compound could exhibit limited solubility.

In summary, the solubility of 2-(1-carboxyethylamino)pentanoic acid is significantly influenced by its structural features and the environment in which it is placed. This makes it a fascinating subject for study in various solvent systems.

Interesting facts

Interesting Facts About 2-(1-Carboxyethylamino)pentanoic Acid

2-(1-Carboxyethylamino)pentanoic acid, often referred to as a derivative of amino acids, exhibits intriguing characteristics that highlight its importance in both biological systems and potential applications. Here are some compelling facts about this compound:

Amino Acid Derivative: This compound can be classified as an amino acid due to its amine and carboxylic acid functional groups, which play a crucial role in various metabolic processes.
Biological Significance: Amino acids are vital for the synthesis of proteins, and derivatives like this one can serve as intermediates in metabolic pathways, potentially influencing the body's physiology.
Synthesis Routes: Scientists often explore various synthesis pathways to create this compound, making it a point of interest for research in organic chemistry and pharmaceutical applications.
Potential Therapeutic Uses: Compounds with similar structures are being investigated for their therapeutic properties, including roles in treating metabolic disorders and neurological conditions.
Structural Diversity: The unique structure, with the branched chain and the carboxyethylamino group, allows for various interactions in biochemical systems, making it a subject of study.

As a student or a scientist delving into the realm of organic and medicinal chemistry, the exploration of 2-(1-carboxyethylamino)pentanoic acid opens up discussions about:

How slight modifications to a compound's structure can drastically alter its biological function.
The role of amino acid derivatives in protein folding and function.
Contributions to the development of new drugs targeting specific metabolic pathways.

In conclusion, the study of 2-(1-carboxyethylamino)pentanoic acid not only enhances our understanding of organic chemistry but also bridges the gap between chemical structure and biological function, emphasizing the intricate relationships within biochemistry.

Synonyms

SCHEMBL5940872