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N-Acetylserine

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Identification
Molecular formula
C7H13NO5
CAS number
123-94-4
IUPAC name
2-(3-carboxypropanoylamino)-5-hydroxy-pentanoic acid
State
State

At room temperature, N-Acetylserine is in a solid state.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.00
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.00
General information
Molecular weight
175.18g/mol
Molar mass
175.1760g/mol
Density
1.5000g/cm3
Appearence

N-Acetylserine typically appears as a white crystalline powder.

Comment on solubility

Solubility of 2-(3-carboxypropanoylamino)-5-hydroxy-pentanoic acid

The solubility of 2-(3-carboxypropanoylamino)-5-hydroxy-pentanoic acid (C7H13NO5) can be influenced by several factors due to its complex structure.

Factors Affecting Solubility

  • Polarity: The presence of multiple functional groups, such as carboxylic acid and amino groups, contributes to its overall polarity, impacting its solubility in polar solvents like water.
  • pH levels: The ionization of the carboxylic acid group can be significantly affected by pH, which may enhance solubility in basic conditions.
  • Hydrogen bonding: The potential for hydrogen bonding, owing to hydroxyl and amino groups, can facilitate solubility in polar solvents.

“The more polar the compound, the better it dissolves in polar solvents.” This adage holds true for the solubility of this compound in water, where increased polarity leads to better dissolution characteristics. In contrast, solubility in nonpolar solvents is likely to be very low.

Conditions of Solubility

Under typical laboratory conditions, this compound is expected to be:

  • Moderately soluble in aqueous solutions.
  • Potentially soluble in organic solvents that can accept hydrogen bonding.

Overall, 2-(3-carboxypropanoylamino)-5-hydroxy-pentanoic acid demonstrates interesting solubility behavior that warrants further exploration, particularly in the context of its applications in biochemical settings.

Interesting facts

Interesting Facts about 2-(3-Carboxypropanoylamino)-5-hydroxy-pentanoic acid

2-(3-Carboxypropanoylamino)-5-hydroxy-pentanoic acid is a fascinating compound that belongs to the family of amino acids and is a significant intermediate in various biochemical pathways. Here are some key points to consider:

  • Biological Significance: This compound plays a crucial role in the metabolic process, particularly in amino acid biosynthesis and degradation.
  • Structural Features: The compound contains both a carboxylic acid group and an amine functional group, highlighting its potential to participate in diverse biochemical reactions, making it amphoteric (able to act both as an acid and a base).
  • Hydroxyl Group: The presence of a hydroxyl group contributes to the compound's reactivity and interaction with other biomolecules, which could be essential in developing therapeutic agents.
  • Research Applications: Scientists are exploring its potential in drug development, nutritional studies, and understanding metabolic disorders due to its structural resemblance to other essential nutrients.

As a researcher, understanding the nuances of such compounds is vital for advancing chemistry and its applications in medicine and nutrition. "The study of compounds like these can lead to groundbreaking discoveries in health and disease management." Always remember, each compound tells a story of its own, uncovering mysteries at the molecular level!