Skip to main content

Acetylhomoserine

ADVERTISEMENT
Identification
Molecular formula
C6H11NO4
CAS number
808-26-0
IUPAC name
4-acetoxy-2-amino-butanoic acid
State
State

Acetylhomoserine is typically found in a solid state under room temperature conditions. Like many amino acids, it is stable and maintains its solid form unless subjected to conditions involving solubility in water or extreme temperature changes.

Melting point (Celsius)
129.00
Melting point (Kelvin)
402.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
175.18g/mol
Molar mass
175.1840g/mol
Density
1.2300g/cm3
Appearence

Acetylhomoserine appears as a white crystalline solid. The crystalline structure forms well-defined particles that can reflect light, giving it a distinct sheen.

Comment on solubility

Solubility of 4-acetoxy-2-amino-butanoic acid

The solubility of 4-acetoxy-2-amino-butanoic acid (C6H11NO4), also known for its intriguing biochemical properties, can be quite significant in various solvents. Here are some factors that influence its solubility:

  • Polar vs. Non-Polar Solvents: This compound contains both polar and non-polar functional groups, suggesting it may be soluble in polar solvents such as water, as well as in organic solvents.
  • pH Dependency: Being an acid, its solubility may also change with pH levels. At lower pH (more acidic), it can form ions, enhancing its solubility in aqueous solutions.
  • Temperature Effects: Like many organic acids, increasing the temperature can increase solubility, allowing for a greater dissolution rate in both polar and non-polar solvents.

In summary, while 4-acetoxy-2-amino-butanoic acid is expected to exhibit good solubility in a range of solvents, the exact solubility can vary widely based on specific conditions. As with all chemical compounds, understanding the solvent interactions is crucial for predicting its behavior in solution.

Interesting facts

Interesting Facts about 4-Acetoxy-2-amino-butanoic Acid

4-Acetoxy-2-amino-butanoic acid, often referred to in the realm of biochemical research, is an intriguing compound that plays a significant role in various fields, particularly in pharmaceuticals and organic synthesis. Here are some engaging highlights about this chemical:

  • Biological Relevance: This compound serves as a derivation of amino acids, making it a valuable intermediate in the synthesis of more complex biomolecules.
  • Potential Therapeutic Uses: Researchers are investigating its properties for potential applications in drug development, particularly in anti-inflammatory and neuroprotective therapies.
  • Functional Groups: The presence of both an amino group and an acetoxy group in its structure allows it to exhibit unique chemical reactivity, which can be advantageous in synthesizing novel compounds.
  • Chirality: As a molecule with stereocenters, 4-acetoxy-2-amino-butanoic acid can exist in different enantiomeric forms, impacting its biological activity and interactions.
  • Research Interest: Due to its potential biological properties, this compound has attracted attention in medicinal chemistry, prompting studies aimed at understanding its mechanisms of action.

In essence, 4-acetoxy-2-amino-butanoic acid exemplifies the fascinating intersection of organic chemistry and biological function. Ongoing research into this compound may pave the way for innovative therapeutic approaches, making it a compound to watch in the scientific community.

Synonyms
4-acetyloxy-2-aminobutanoic acid
4-Acetoxy-2-aminobutanoic acid
Homoserine acetate
O-acetyl-dl-homoserine
SCHEMBL302495
CHEBI:7671
HAA54067
4-(acetyloxy)-2-aminobutanoic acid
Q27107556