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L-Leucyl-D-alanine

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Identification
Molecular formula
C9H18N2O3
CAS number
6693-36-7
IUPAC name
2-(3-aminopropanoylamino)-4-methyl-pentanoic acid
State
State

At room temperature, this compound is a solid.

Melting point (Celsius)
278.00
Melting point (Kelvin)
551.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
188.23g/mol
Molar mass
188.2290g/mol
Density
1.2900g/cm3
Appearence

This compound is typically a white crystalline powder.

Comment on solubility

Solubility of 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid

The solubility of 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid (C9H18N2O3) is influenced by its molecular structure and functional groups.

Key Factors Affecting Solubility:

  • Polarity: Due to the presence of amine and carboxylic acid groups, this compound is expected to exhibit high polarity, enhancing its solubility in polar solvents, particularly water.
  • Hydrogen Bonding: The potential for hydrogen bonding between the carboxylic acid group and water molecules further increases solubility in aqueous solutions.
  • Hydrophobic Interactions: The presence of the methyl and alkyl groups may introduce some hydrophobic character, which can affect solubility, particularly in non-polar solvents.

Overall, it is anticipated that this compound is moderately soluble in water while displaying reduced solubility in non-polar organic solvents. According to the principles of solubility, “like dissolves like,” thus polar solvents will dissolve this compound more readily than non-polar substances.

Interesting facts

Interesting Facts about 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid

2-(3-aminopropanoylamino)-4-methyl-pentanoic acid, often referred to as a derivative of amino acids, is a fascinating compound that intersects various fields like biochemistry, medicinal chemistry, and nutrition. Here are some intriguing highlights:

  • Amino Acid Connection: This compound can be categorized as an α-amino acid, meaning it contains both an amino group and a carboxylic acid group. Such structural features allow this compound to participate in many biological reactions.
  • Structural Diversity: The presence of both an amino group (-NH2) and an additional functional group contributes to its unique structural properties. This intricacy supports diverse biological functions, playing a crucial role in protein synthesis and metabolism.
  • Potential Therapeutic Uses: Similar to other amino acid derivatives, 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid holds promise in pharmaceutical research. Researchers are investigating potential applications such as neuroprotective agents and metabolic modulating drugs.
  • Natural Sources: Many amino acid derivatives have been sourced from natural proteins and peptides, hinting at a deeper biochemical significance in organisms. Exploring these natural origins can pave the way for new findings in biochemistry.
  • Research Feasibility: Scientists are constantly exploring amino acid derivatives due to their abundance and diverse reactivity. This compound is likely being investigated in laboratories worldwide for its role in various biochemical pathways.

Overall, 2-(3-aminopropanoylamino)-4-methyl-pentanoic acid exemplifies the remarkable complexity and utility of amino acid derivatives in both nature and scientific research. As chemists continue to unlock its potential, the implications for health and industry could be significant.

Synonyms
H-BETA-ALA-DL-LEU-OH
102029-56-1
2-(3-aminopropanoylamino)-4-methylpentanoic acid
2-(3-aminopropanamido)-4-methylpentanoic acid
Beta-alanyl-dl-leucine
N-(3-aminopropanoyl)leucine
SPBio_001567
Spectrum2_001354
Spectrum4_000816
Spectrum4_001195
KBioGR_001331
KBioGR_001889
DivK1c_000223
SCHEMBL6447009
CHEMBL3039404
HMS500L05
KBio1_000223
NINDS_000223
CCG-39292
AKOS010404076
IDI1_000223
PD118920
DB-043863