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Citrulline

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Identification
Molecular formula
C6H13N3O3
CAS number
372-75-8
IUPAC name
2-(1-carboxyethylamino)-5-guanidino-pentanoic acid
State
State

Citrulline is typically encountered as a solid at room temperature. It is often found in dietary supplements as a flavorless powder that is easy to dissolve in water or other liquids.

Melting point (Celsius)
213.00
Melting point (Kelvin)
486.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
175.19g/mol
Molar mass
175.1880g/mol
Density
1.4240g/cm3
Appearence

Citrulline is a white crystalline solid at room temperature. It is often available in powder form for supplement use. The compound is known for its solubility in water.

Comment on solubility

Solubility of 2-(1-carboxyethylamino)-5-guanidino-pentanoic acid

The solubility of 2-(1-carboxyethylamino)-5-guanidino-pentanoic acid (C6H13N3O3), also known as a unique amino acid derivative, can be summarized as follows:

  • Water Solubility: This compound exhibits significant solubility in water due to the presence of multiple polar functional groups. The carboxylic acid and amino groups can effectively interact with water molecules, enhancing its solubility.
  • pH Dependency: The solubility of this compound may vary with pH. As a result of its acidic and basic functional groups, the ionization can affect how well it dissolves, especially in different pH environments.
  • Temperature Effects: Increased temperature generally improves solubility for many organic compounds, and 2-(1-carboxyethylamino)-5-guanidino-pentanoic acid may exhibit similar behavior as it dissolves more readily at higher temperatures.

In conclusion, the solubility characteristics of C6H13N3O3 showcase its effective interaction with polar solvents, making it an interesting compound for various applications, particularly in biochemical contexts. As with many compounds, it is important to consider environmental factors such as temperature and pH to fully understand its solubility behavior.

Interesting facts

Interesting Facts about 2-(1-carboxyethylamino)-5-guanidino-pentanoic Acid

2-(1-carboxyethylamino)-5-guanidino-pentanoic acid, often referred to as a specific derivative of amino acids, is a compound with fascinating functionalities in biological systems. Here are some key points that make this compound particularly interesting:

  • Biological Role: This compound plays a significant role in various metabolic pathways, particularly in the synthesis of creatine, which is crucial for energy storage in muscles.
  • Amino Acid Derivative: As an amino acid derivative, it shares similarities with other amino acids, making it vital in protein synthesis and cellular functions.
  • Potential Therapeutic Applications: Research suggests that compounds similar to this one may have therapeutic effects, including potential applications in muscle wasting conditions or metabolic disorders.
  • Research Scope: Scientists studying amino acid metabolism often focus on this compound to understand its biochemical pathways and implications in various diseases.
  • Structural Complexity: The intricate structure, including the guanidino group, significantly contributes to its biochemical activity and interactions with other biomolecules.

In summary, 2-(1-carboxyethylamino)-5-guanidino-pentanoic acid is not just a simple compound; it is a vital part of the intricate web of biochemistry that sustains life. As noted by researchers, "Understanding the nuances of such compounds can unlock new avenues for medical breakthroughs." Its study encapsulates the beauty of chemistry, biology, and the potential for future advancements in health and medicine.

Synonyms
2-(1-carboxyethylamino)-5-(diaminomethylideneamino)pentanoic acid
SCHEMBL638492
5-(amidinoamino)-2-[(carboxyethyl)amino]pentanoic acid
CHEBI:182149
NSC367090
AKOS015893948
NSC-367090
Q2013941