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N-Acetylserine

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Identification
Molecular formula
C8H15NO5
CAS number
13215-37-5
IUPAC name
4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-2-hydroxy-butanoic acid
State
State

At room temperature, N-Acetylserine is generally in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
173.00
Melting point (Kelvin)
446.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
191.20g/mol
Molar mass
191.1990g/mol
Density
1.2470g/cm3
Appearence

N-Acetylserine typically appears as a white crystalline powder.

Comment on solubility

Solubility of 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-2-hydroxy-butanoic acid

The solubility of 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-2-hydroxy-butanoic acid, a complex organic compound, can be influenced by several factors such as pH, temperature, and the nature of the solvent used.

Factors Affecting Solubility

  • pH Level: The presence of acidic or basic groups in the compound can lead to changes in solubility. For example, in more acidic conditions, the carboxylic acid group may remain protonated, affecting the overall solubility.
  • Temperature: Typically, an increase in temperature can enhance the solubility of most solids in liquids, which may also apply to this compound.
  • Solvent Polarity: The solubility is often higher in polar solvents (like water) compared to nonpolar solvents due to the ionic and polar nature of the compound.

“Like dissolves like” is a fundamental principle in chemistry that indicates that polar compounds tend to dissolve in polar solvents, while nonpolar compounds dissolve in nonpolar solvents.

Predicted Solubility

Considering the presence of multiple hydroxyl groups and a carboxylic acid functional group, it is anticipated that this compound may exhibit:

  • Moderate solubility in water due to its polar characteristics.
  • Lower solubility in organic solvents such as hexane or toluene, which lack polarity.

Overall, understanding the solubility behavior of this compound is critical for its applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-2-hydroxy-butanoic acid

This fascinating compound, known for its complex structure and potential bioactivity, dives into the world of amino acids and their derivatives. Here are some engaging insights:

  • Derivative of Amino Acids: This compound features an amino acid backbone, showcasing how structural modifications can lead to varied biological activities, which helps chemists understand enzyme interactions and metabolic pathways.
  • Hydroxyl Groups: The presence of multiple hydroxyl groups in its structure can enhance solubility and reactivity, making it a subject of interest for researchers focusing on drug design and medicinal chemistry.
  • Biological Implications: Compounds like this one can act as intermediates in the synthesis of pharmaceuticals, potentially influencing the development of treatments for various diseases.
  • Natural Occurrence: This compound's analogs are often found in nature, particularly in certain plant species, which can lead to exciting discoveries in phytochemistry and the study of natural products.

In summary, 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-2-hydroxy-butanoic acid serves as an intriguing example of how chemical modifications can yield compounds with significant biological importance. As researchers continue to explore its properties, the compound may unveil new pathways in both synthetic and medicinal chemistry.

Synonyms
alpha-Oxy-hopa
alpha-Hydroxyhomopantothenic acid
4-(2,4-Dihydroxy-3,3-dimethylbutyramido)-2-hydroxybutyric acid
1977-34-0
Butanoic acid, 4-((2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)amino)-2-hydroxy-
BUTYRIC ACID, 4-(2,4-DIHYDROXY-3,3-DIMETHYLBUTYRAMIDO)-2-HYDROXY-
DTXSID60941541
2-Hydroxy-4-[(1,2,4-trihydroxy-3,3-dimethylbutylidene)amino]butanoic acid