Interesting facts
Interesting Facts about 2-(Ethylamino)butanedioic Acid
2-(Ethylamino)butanedioic acid, often referred to in research contexts for its diverse applications, showcases a unique structural makeup that is crucial for its biological significance. Here are some remarkable aspects of this compound:
- Biological Role: This compound acts as a precursor in various biosynthetic pathways, especially in the synthesis of important amino acids and neurotransmitters.
- Synthetic Applications: It is utilized in the production of pharmaceuticals, particularly those targeting neurological disorders, owing to its ability to cross the blood-brain barrier.
- Structural Characteristics: The presence of an ethylamine group enhances its reactivity, making it a valuable starting material in organic synthesis.
- Potential as a Nutraceutical: 2-(Ethylamino)butanedioic acid has been explored for its potential health benefits, particularly concerning metabolic pathways and muscle performance.
- Research Frontier: Researchers are investigating its roles in various chemical reactions, which could lead to the development of novel catalysts or therapeutic agents.
As a chemistry student, understanding the multifaceted nature of compounds like 2-(ethylamino)butanedioic acid can not only enhance your grasp of organic chemistry but also open avenues for innovative discoveries in pharmacology and biochemistry.
“Chemistry is not just about what you can see, but about what you can imagine.” This quote underpins the significance of exploring compounds like 2-(ethylamino)butanedioic acid, as each molecule holds the potential for transformative applications in science.
Synonyms
N-Ethyl-DL-aspartic acid
5555-23-7
ASPARTIC ACID, N-ETHYL-, DL-
DL-Etielas partiensuur
DL-N-Ethylasparatic acid
N-ethyl-D-aspartic acid
2-(ethylamino)butanedioic acid
N-ethylaspartic acid
SCHEMBL11131045
DTXSID00970890
Solubility of 2-(ethylamino)butanedioic acid
2-(ethylamino)butanedioic acid, a compound belonging to the class of amino acids, exhibits interesting solubility properties primarily influenced by its functional groups and molecular structure. The presence of both carboxylic acid groups and an amino group enhances its ability to interact with water through hydrogen bonding, making it generally soluble in polar solvents. Here are some important points regarding its solubility:
As a general rule, the more ionic or polar the solvent, the greater the solubility of 2-(ethylamino)butanedioic acid. This is a classic example of the principle that 'like dissolves like'. To better understand its implications in different environments, scientists often term it a "bifunctional" molecule due to its diverse interactions in aqueous solutions.