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N-Acetyl-L-ornithine

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Identification
Molecular formula
C7H14N2O3
CAS number
1949-84-8
IUPAC name
2-acetamido-5-amino-pentanoic acid
State
State

At room temperature, N-Acetyl-L-ornithine is in a solid state.

Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
518.30
Boiling point (Kelvin)
791.50
General information
Molecular weight
188.21g/mol
Molar mass
188.2070g/mol
Density
1.2900g/cm3
Appearence

N-Acetyl-L-ornithine appears as a white crystalline powder. It is commonly used in scientific studies and biochemical applications.

Comment on solubility

Solubility of 2-Acetamido-5-Amino-Pentanoic Acid

2-Acetamido-5-amino-pentanoic acid, with the chemical formula C7H14N2O3, exhibits notable solubility characteristics, primarily owing to its polar functional groups.

Key Insights on Solubility:

  • Polar Nature: The presence of both acetamido and amino groups contributes to its polarity, making it more soluble in polar solvents such as water.
  • Hydrophilic Interactions: The ability of this compound to form hydrogen bonds with water molecules enhances its solubility, promoting better interaction in solution.
  • pH Dependence: The solubility may vary with pH. Under acidic or alkaline conditions, ionization of the amino or carboxylic acid groups could significantly influence the compound's solubility profile.

To summarize, the solubility of 2-acetamido-5-amino-pentanoic acid is largely favorable in aqueous environments due to its functional groups, which promote solvation through polar and ionic interactions. “Solubility is key for biological activity and bioavailability,” revealing its relevance in pharmacological and biochemical applications.

Interesting facts

Interesting Facts about 2-Acetamido-5-amino-pentanoic acid

2-Acetamido-5-amino-pentanoic acid, commonly known in the scientific community as a derivative of amino acids, is notable for its unique structural characteristics and functions. Here are several intriguing facts about this compound:

  • Amino Acid Precursor: This compound acts as a precursor to essential amino acids, playing a critical role in protein synthesis and metabolism.
  • Biological Importance: It is key in several biochemical pathways, particularly those involving the synthesis of other biologically active molecules.
  • Research Applications: Scientists have studied 2-acetamido-5-amino-pentanoic acid in various research contexts, particularly in pharmaceutical chemistry and biochemistry, investigating its potential therapeutic effects.
  • Structural Insights: The compound features an acetamido group, which contributes to its reactivity and interactions with biological systems.
  • Conformational Flexibility: The presence of multiple amino and carboxyl groups allows for significant conformational variability, impacting how it interacts with enzymes or receptor sites.

As chemists delve deeper into derivatives like 2-acetamido-5-amino-pentanoic acid, they reveal not only its unique properties but also its potential contributions to health and medicine. In the words of one researcher, “The understanding of amino acid derivatives like this compound opens new avenues for the development of targeted therapies.”

Exploring these compounds further may lead to advancements in fields such as nutrition and drug development, with implications too significant to overlook.

Synonyms
N-Acetyl-ornithine
2-acetamido-5-aminopentanoic acid
Ornithine, N2-acetyl-
N-acetyl-L-ornithine
8-acetylornithine
Ac-L-Orn-OH
SCHEMBL159459
CHEBI:181895
FA47655
DB-054048
NS00014889
55306BF3-CC8D-471E-802A-D00B5EA623FC