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L-Arginine

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Identification
Molecular formula
C6H14N4O2
CAS number
74-79-3
IUPAC name
2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid
State
State

At room temperature, L-Arginine is in a solid state. It is categorized as an α-amino acid commonly found in animal proteins.

Melting point (Celsius)
260.00
Melting point (Kelvin)
533.15
Boiling point (Celsius)
302.00
Boiling point (Kelvin)
575.15
General information
Molecular weight
174.20g/mol
Molar mass
174.2010g/mol
Density
1.0500g/cm3
Appearence

Arginine typically appears as a white crystalline powder. It is odorless or may have a slight ammonia-like odor. In its crystalline form, it is highly soluble in water, allowing it to dissolve easily.

Comment on solubility

Solubility of 2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid

The solubility of 2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid, with the chemical formula C6H14N4O2, is influenced by several factors due to its unique functional groups. The compound contains both amino and carbamimidoyl groups, which can affect its interactions with solvents. Here's what to consider:

  • Polar Nature: The presence of multiple nitrogen and oxygen atoms indicates a polar character in the molecule, suggesting that it is likely soluble in polar solvents such as water.
  • Hydrogen Bonding: The amino groups present allow for extensive hydrogen bonding with water molecules, enhancing solubility.
  • Conformational Flexibility: The structure of the compound permits interactions with solvent molecules, further aiding in its solubility.

It is essential to note that while the aforementioned factors predict a reasonable solubility in polar solvents, the specific conditions such as temperature and pH can also play significant roles in the actual solubility observed. Therefore, it is often recommended to conduct experimental investigations to determine precise solubility values in various environments.

Interesting facts

Interesting Facts About 2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic Acid

2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid, often referred to by its common name, is a fascinating compound in the realm of biochemistry and medicinal chemistry. This compound is classified as an amino acid derivative and exhibits unique properties that contribute to its significance in various scientific fields.

Key Characteristics

  • Amino Acid Functionality: As an amino acid derivative, this compound plays an essential role in protein structure and function.
  • Biological Importance: It has been investigated for potential therapeutic applications, particularly in the field of pharmaceuticals.
  • Catalytic Properties: Research shows that compounds with similar structures can act as catalysts in certain biochemical reactions, enhancing reaction rates.

This compound's unique structure includes a N'-methylcarbamimidoyl group, which may contribute to its biological activity and interaction with various enzymes and receptors in the body. The presence of this group enhances its ability to mimic the natural substrates in metabolic pathways, making it an interesting candidate for drug design.

Research Over the Years

Studies have suggested that derivatives like 2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid may provide insights into:

  1. Enzyme Inhibition: Understanding how this compound interacts with enzymes can lead to the development of novel inhibitors for therapeutic use.
  2. Metabolic Pathways: Analyzing its role in specific metabolic pathways can uncover new potential targets for drug development.
  3. Structure-Activity Relationships: Research into its structure can help inform the design of more effective analogs.

In summary, 2-amino-5-[(N'-methylcarbamimidoyl)amino]pentanoic acid is more than just a simple amino acid derivative. Its complex structure and functional groups render it a valuable subject of study, with potential applications in areas such as drug discovery and metabolic research. The exploration of this compound offers a window into the intricate world of biochemistry and the ongoing quest for innovative therapeutics.

Synonyms
Methylarginine
CHEMBL312870
H-Arg(Me)-OH acetate salt
L-NMMA;Tilarginine;Targinine
Ng-METHYL-L-ARGININE ACETATE
t-arginine
8-monomethylarginine
nomega-methyl-l-arginine
2-Amino-5-(N''-methyl-guanidino)-pentanoic acid
Spectrum2_001482
Spectrum3_001522
Spectrum4_000549
Spectrum5_001717
BSPBio_002904
KBioGR_001217
DivK1c_001002
SPBio_001463
SCHEMBL7450191
SCHEMBL10198569
SCHEMBL23099403
KBio1_001002
KBio3_002404
DTXSID50860196
NINDS_001002
BDBM50030279
NSC683245
NSC-683245
IDI1_001002
NCGC00015698-02
2aAminoa5a(N'amethylcarbamimidamido)pentanoic acid
Q6823955