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N-Lauroylvaline

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Identification
Molecular formula
C17H33NO3
CAS number
5720-71-2
IUPAC name
(2S)-2-(dodecanoylamino)-3-methyl-butanoic acid
State
State

At room temperature, N-Lauroylvaline is typically found in a solid state. Its well-defined crystalline form is stable under standard laboratory conditions.

Melting point (Celsius)
69.00
Melting point (Kelvin)
342.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
299.45g/mol
Molar mass
299.4730g/mol
Density
0.9302g/cm3
Appearence

N-Lauroylvaline is typically a white crystalline powder. Its appearance may vary slightly depending on the purity and specific preparation method used in the laboratory.

Comment on solubility

Solubility of (2S)-2-(dodecanoylamino)-3-methyl-butanoic acid

The solubility characteristics of (2S)-2-(dodecanoylamino)-3-methyl-butanoic acid can be influenced by various factors, including its molecular structure and the presence of functional groups. Here are some critical points to consider:

  • Amphiphilic Nature: The compound possesses both hydrophilic (water-loving) and hydrophobic (water-fearing) regions, which suggests that it can interact with both polar and non-polar solvents.
  • Solvent Interaction: It is expected to be soluble in organic solvents like ethanol and chloroform, while its solubility in water may be limited due to the long dodecanoyl chain.
  • pH Dependence: The solubility might vary with pH, especially considering the presence of acidic functional groups; they can ionize in basic conditions, potentially increasing water solubility.

In summary, while (2S)-2-(dodecanoylamino)-3-methyl-butanoic acid exhibits amphiphilic properties, its solubility profile tends to favor organic solvents over aqueous solutions, emphasizing the importance of the chemical environment in determining solubility.

Interesting facts

Interesting Facts about (2S)-2-(Dodecanoylamino)-3-methyl-butanoic Acid

(2S)-2-(Dodecanoylamino)-3-methyl-butanoic acid, often referred to in the scientific community as a sophisticated amino acid derivative, has garnered attention for its unique structure and potential applications. Here are some intriguing points worth noting:

  • Amino Acid Derivative: This compound is classified as an amino acid derivative, which means it plays a crucial role in biochemistry, mirroring the structure and functionality of natural amino acids.
  • Biological Relevance: The amide group, derived from dodecanoyl, indicates that this compound may participate in lipid-related biological processes, hinting at potential applications in metabolic studies.
  • Natural Products: Given its resemblance to naturally occurring compounds, scientists are investigating its role in synthetic biology and its potential to mimic or enhance metabolic pathways.
  • Research Potential: Research is ongoing into its influence on various cellular mechanisms. The structural complexity could lead to findings that may enhance our understanding of protein synthesis and modifications.
  • Pharmaceutical Interest: Compounds like this are often of interest in drug design due to their possible therapeutic effects, particularly in developing molecules that interact with receptors in innovative ways.

In brief, (2S)-2-(dodecanoylamino)-3-methyl-butanoic acid exemplifies the intricate interplay between structure and function within biological systems. Its continued study may unlock new avenues in both chemistry and medicine. As the renowned chemist Linus Pauling once noted, “The best way to have a good idea is to have a lot of ideas.” This compound certainly adds to that pool of innovative possibilities.

Synonyms
14379-28-3
N-(1-OXODODECYL)-L-VALINE
N-lauroyl-L-valine
L-Valine, N-(1-oxododecyl)-
(2S)-2-(dodecanoylamino)-3-methylbutanoic acid
N-DODECANOYL-VALINE
N-lauroylvaline
N-dodecanoyl-l-val
SCHEMBL2636223
N-(1-Hydroxydodecylidene)valine
DTXSID10932101
WQHXCNGQDLRDMP-INIZCTEOSA-N
AKOS014787207