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2-Aminoisobutyric Acid

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Identification
Molecular formula
C4H9NO2
CAS number
62-57-7
IUPAC name
2-amino-2-methyl-butanedioic acid
State
State

At room temperature, 2-aminoisobutyric acid is a solid.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
131.16g/mol
Molar mass
131.1570g/mol
Density
1.0419g/cm3
Appearence

2-Aminoisobutyric acid appears as a white crystalline solid or powder. It is typically odorless and has a slight sweet taste.

Comment on solubility

Solubility of 2-amino-2-methyl-butanedioic acid (C4H9NO2)

2-amino-2-methyl-butanedioic acid, commonly known as branched-chain amino acid, exhibits interesting solubility properties that are worth noting:

  • It is generally soluble in water due to the presence of both amino and carboxylic acid functional groups, which can engage in hydrogen bonding with water molecules.
  • The solubility may vary with temperature, usually increasing as the temperature rises, which is a common trait among amino acids.
  • In organic solvents, its solubility is substantially lower, reflecting its polar nature.

In summary: 2-amino-2-methyl-butanedioic acid demonstrates good water solubility while being less soluble in organic solvents. Understanding these solubility characteristics is essential for applications in biochemical processes and formulations.

Interesting facts

Interesting Facts about 2-Amino-2-methyl-butanedioic acid

2-Amino-2-methyl-butanedioic acid, more commonly known as amino acid derivatives, holds a significant place within the realm of biochemistry and nutritional science. This compound is particularly noteworthy due to its role as a precursor to various biochemical pathways, influencing protein synthesis and metabolic processes.

Key Aspects of 2-Amino-2-methyl-butanedioic acid

  • Building Block of Proteins: Like other amino acids, this compound contributes to the formation of proteins by serving as a monomer in polypeptide chains.
  • Metabolic Role: It plays a pivotal role in various metabolic pathways, enhancing muscle growth and recovery, which is why it is often found in dietary supplements.
  • Influence on Health: The compound is closely studied for its potential benefits in exercise performance and muscle maintenance, making it a focal point in athletic nutrition.
  • Synthesis: This amino acid can be synthesized through both natural and laboratory methods, allowing for its use in various research and industrial applications.

Additionally, 2-Amino-2-methyl-butanedioic acid exemplifies the fascinating interplay between chemistry and health, highlighting how a single compound can influence a myriad of biological functions. As noted by prominent scientists, “The building blocks of life are not just the atoms of the elements, but the compounds they form and the interplay between them.”

Thus, understanding this amino acid and its properties not only enriches our knowledge of biochemical processes but also enhances our ability to develop nutritional strategies for improved health and performance.

Synonyms
2-Amino-2-methylsuccinic acid
2792-66-7
alpha-Methyl-DL-aspartic acid
2-Methyl-DL-aspartic acid
2-Methylaspartic acid
DL-Aspartic acid, 2-methyl-
70W4HTK6W3
NSC-153559
2-amino-2-methylbutanedioic acid
alpha-Methyl-DL-aspartate
DL-2-Methylaspartic acid
UNII-70W4HTK6W3
DL-alpha-Methylaspartic acid
NSC 153559
Aspartic acid, 2-methyl-, DL-
alpha-methylaspartic acid
866-73-9
NSC14963
dl-2-Amino-2-methylsuccinic acid hydrate
|A-Methyl-DL-aspartic acid
MFCD00216906
MFCD00056709
NSC153559
beta-Me-DL-Asp-OH
?-Me-DL-Asp-OH
2-Methylaspartic acid #
l-alpha-methylaspartic acid
?-Methyl-DL-aspartic acid
ASPARTIC ACID, L-THREO
SCHEMBL1660876
NSC D16206
.ALPHA.-METHYLASPARTIC ACID
CAA79266
MFCD00145254
NSC-14963
AKOS006228860
Aspartic acid, beta-methyl, --threo-
DL-.ALPHA.-METHYLASPARTIC ACID
HY-W142119
.ALPHA.-METHYL-DL-ASPARTIC ACID
SY265707
SY271892
DB-018060
DB-048191
DB-227188
CS-0201902
E82409
Q27896228