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Homoarginine

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Identification
Molecular formula
C8H15NO4
CAS number
23277-43-2
IUPAC name
3-(carboxymethyl)-4-isopropyl-pyrrolidine-2-carboxylic acid
State
State

At room temperature, Homoarginine is in a solid state. It is often encountered as a dry powder and is stable under normal laboratory conditions.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.15
Boiling point (Celsius)
275.50
Boiling point (Kelvin)
548.50
General information
Molecular weight
159.19g/mol
Molar mass
159.1880g/mol
Density
1.3210g/cm3
Appearence

Homoarginine appears as a white crystalline powder. It is typically not associated with any distinct odor and is often used in biochemical applications as a substrate or reagent.

Comment on solubility

Solubility of 3-(carboxymethyl)-4-isopropyl-pyrrolidine-2-carboxylic acid

The solubility of 3-(carboxymethyl)-4-isopropyl-pyrrolidine-2-carboxylic acid, with the chemical formula C8H15NO4, can be influenced by several factors:

  • Polarity: Given the presence of multiple carboxylic acid groups in its structure, this compound exhibits polar characteristics. Polar compounds tend to dissolve well in polar solvents, such as water.
  • Temperature: The solubility of organic compounds often increases with temperature. Therefore, heating the solvent might enhance the dissolution of this compound.
  • pH Levels: As a carboxylic acid, the solubility may also be affected by the pH of the solution. At higher pH levels, deprotonation can increase the solubility.
  • Chain Length: The branched isopropyl group may introduce hydrophobic characteristics; however, the overall structure remains primarily hydrophilic due to the carboxyl groups.

In summary, while this compound shows potential for good solubility in polar solvents especially under favorable conditions, the specific solubility will depend on the balance between its hydrophilic and hydrophobic regions, as well as the environmental factors like temperature and pH.

Interesting facts

Interesting Facts about 3-(Carboxymethyl)-4-isopropyl-pyrrolidine-2-carboxylic Acid

3-(Carboxymethyl)-4-isopropyl-pyrrolidine-2-carboxylic acid, often referred to as a specialized amino acid derivative, holds significant interest in the fields of biochemistry and pharmacology. Here are some captivating insights about this compound:

  • Dual Functional Groups: This compound features both carboxylic acid groups which are vital for its reactivity and interaction with biological systems, making it a subject of study for drug design.
  • Structural Diversity: The isopropyl group contributes distinct steric effects, influencing its physical and chemical properties, particularly its reactivity and solubility in different solvents.
  • Biological Relevance: Compounds with similar structures are often involved in key metabolic processes and can act as amino acid analogs, providing potential therapeutic effects.
  • Potential Applications: Due to its structural attributes, this compound may be explored for use in:
    • Medicinal chemistry for developing new drugs
    • Biocatalysis and enzyme technology
    • Peptide synthesis and modification
  • Research Avenues: Ongoing studies focus on:
    • The role of similar compounds in metabolic pathways
    • Investigating their interactions with biological macromolecules
    • Exploring modifications that enhance their drug-like properties

This compound serves as an exemplary model for understanding complex biochemical interactions and illustrates the interplay between structure and function in organic chemistry. As we continue to explore its properties, it offers exciting prospects for future research and applications in pharmacology and biotechnology.

Synonyms
3-(carboxymethyl)-4-isopropylpyrrolidine-2-carboxylic acid
alpha-Dihydrokainic acid
-Dihydrokainic acid
2-Carboxy-4-isopropyl-3-pyrrolidineacetic acid
MFCD03412037
DB-052132
5626-44-8