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L-Alanine β-alanine ester

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Identification
Molecular formula
C7H15NO3
CAS number
218099-40-0
IUPAC name
2-aminobutyl 2-hydroxypropanoate
State
State

At room temperature, it is typically found as a liquid.

Melting point (Celsius)
12.50
Melting point (Kelvin)
285.65
Boiling point (Celsius)
249.30
Boiling point (Kelvin)
522.45
General information
Molecular weight
145.18g/mol
Molar mass
145.1830g/mol
Density
1.1000g/cm3
Appearence

A colorless to pale yellow liquid that is hygroscopic.

Comment on solubility

Solubility of 2-aminobutyl 2-hydroxypropanoate

2-aminobutyl 2-hydroxypropanoate, a compound featuring both an amino group and a hydroxyl group, showcases distinct solubility characteristics that are essential for its applications. Generally, the solubility of organic compounds like this one is influenced by several factors, including:

  • Functional Groups: The presence of amino and hydroxyl groups tends to increase water solubility due to hydrogen bonding capabilities.
  • Molecular Weight: Lower molecular weight compounds often exhibit higher solubility in water; thus, 2-aminobutyl 2-hydroxypropanoate is likely to dissolve significantly.
  • Polarity: The molecular structure is relatively polar, enhancing its affinity for polar solvents such as water.

As a result, we can anticipate that 2-aminobutyl 2-hydroxypropanoate is soluble in polar solvents, particularly water. This solubility can be attributed to its ability to form numerous hydrogen bonds with water molecules, leading to an overall favorable dissolution process. In practical terms, such properties make this compound valuable in various chemical applications, especially those requiring sufficient solubility in aqueous environments.

Interesting facts

Interesting Facts about 2-aminobutyl 2-hydroxypropanoate

2-aminobutyl 2-hydroxypropanoate is an intriguing compound with notable significance in both chemistry and biochemistry. Here are some key points to consider:

  • Structure and Function: This compound features an amino group and a hydroxy group, contributing to its potential as a versatile building block in organic synthesis. The presence of these functional groups enables participation in various reactions, including nucleophilic substitutions and esterifications.
  • Biological Relevance: 2-aminobutyl 2-hydroxypropanoate may play a role in metabolic pathways and can act as a precursor for important biomolecules. This can make it valuable in the study of amino acid metabolism and enzymatic reactions.
  • Applications: Its unique properties open up opportunities for use in pharmaceuticals, as well as in the development of biodegradable polymers. Compounds of this nature are often investigated for their potential in creating sustainable materials.
  • Research Potential: Ongoing studies may focus on its reactivity and interaction with various biological systems, which could lead to discoveries in drug development and therapeutic applications.

As a scientific community, we continuously explore compounds like 2-aminobutyl 2-hydroxypropanoate to unravel new chemical reactions and improve our understanding of biological processes. Engaging with such compounds expands our horizons in the fields of organic synthesis and molecular biology.

In the words of a famous chemist, "The beauty of chemistry is the ability to create something extraordinary from the simplest of molecules." Understanding compounds like 2-aminobutyl 2-hydroxypropanoate exemplifies this sentiment, reminding us of the intricate connections within the world of science.