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O-Acetylserine

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Identification
Molecular formula
C5H9NO4
CAS number
O-Acetylserine
IUPAC name
3-acetoxy-2-amino-propanoic acid
State
State

O-Acetylserine is a solid at room temperature, often found in crystalline or powder form. It is stable under standard conditions of temperature and pressure.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
147.13g/mol
Molar mass
147.1330g/mol
Density
1.2900g/cm3
Appearence

O-Acetylserine is typically a white to off-white crystalline solid. It may also appear as a powder depending on its processing and preparation. It has no significant odor.

Comment on solubility

Solubility of 3-acetoxy-2-amino-propanoic acid (C5H9NO4)

3-acetoxy-2-amino-propanoic acid is a fascinating compound when it comes to solubility, demonstrating the impact of its functional groups. The structure contains an amino group, an acetoxy group, and a carboxylic acid component, which contribute significantly to its solubility properties:

  • Hydrophilicity: The presence of both amino and carboxylic acid groups enhances solubility in aqueous environments. These polar functional groups can engage in hydrogen bonding with water molecules.
  • Acid-Base Interaction: The carboxylic acid can donate protons (H+), while the amino group can accept them, facilitating a range of ionic interactions in varying pH levels.
  • Solvent Compatibility: The compound is likely to be soluble in polar solvents such as methanol and ethanol, but may exhibit reduced solubility in non-polar organic solvents.

As a result, you might commonly find 3-acetoxy-2-amino-propanoic acid exhibiting good solubility in physiological conditions, which could be beneficial for various biochemical applications. In practical terms, one might say that "the sum of its functional parts speaks to its ability to interact with water." This characteristic makes it a suitable candidate for studies in biochemistry and pharmacology, while also underlining the fascinating interplay of structure and solubility in chemical compounds.

Interesting facts

Interesting Facts about 3-acetoxy-2-amino-propanoic acid

3-acetoxy-2-amino-propanoic acid, often regarded as a fascinating chemical compound, is notable for its functional versatility, which makes it of great interest in both research and industry. Here are some captivating aspects of this compound:

  • Biological Relevance: This compound can be classified as an amino acid derivative, a category critical in biological systems. Amino acids are the building blocks of proteins, highlighting the importance of such compounds in biochemistry.
  • Synthetic Applications: The acetoxy group enhances its reactivity, enabling the compound to participate in a variety of chemical reactions. This makes it a valuable intermediate in organic synthesis and pharmaceuticals.
  • Research Potential: Its unique structure contributes to potential studies on enzyme activity and metabolic pathways, allowing scientists to track and explore biochemical processes.
  • Analytical Significance: The presence of both amino and acetoxy functional groups facilitates its study using various analytical techniques such as NMR and mass spectrometry, providing insight into molecular interactions and behaviors.
  • Green Chemistry: The synthesis of 3-acetoxy-2-amino-propanoic acid can be approached through environmentally benign methods, aligning with the principles of green chemistry aimed at reducing waste and enhancing efficiency.

Overall, 3-acetoxy-2-amino-propanoic acid stands out as an excellent subject for ongoing studies due to its multifaceted roles in organic chemistry and biological systems. As scientists continue to unravel its complexities, it may yield invaluable insights into both health and industrial applications.

Synonyms
4985-36-8
Serine acetate ester
O-Acetyl-DL-serine
3-acetyloxy-2-aminopropanoic acid
NSC 16549
NSC 408393
3-(acetyloxy)-2-aminopropanoic acid
o-Acetylserine #
NSC-16549
O-acetyl-d,l-serine
Serine, acetate (ester)
DL-Serine, acetate (ester)
SCHEMBL770416
DTXSID00863475
VZXPDPZARILFQX-UHFFFAOYSA-N
NSC16549
NSC226230
NSC231949
NSC408393
NSC-231949
NSC-408393
NS00126207
EN300-6747133
89417-53-8