(S)-2-Amino-2-ethyloctanoic acid, also known as a branched-chain amino acid, is characterized by its chiral center, which imparts specific stereochemical properties. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), making it an α-amino acid. The presence of an ethyl group on the second carbon contributes to its hydrophobic nature, influencing its solubility and interaction with biological systems. It is typically found in a zwitterionic form at physiological pH, where the amino group is protonated and the carboxylic acid group is deprotonated. This compound is of interest in biochemical research and potential therapeutic applications, particularly in the context of protein synthesis and metabolic pathways. Its unique structure may also affect its role in cellular signaling and energy metabolism. As with many amino acids, it is likely to participate in various biochemical reactions, including transamination and peptide bond formation, contributing to the complexity of protein structures and functions in living organisms.

(S)-2-AMINO-2-ETHYLOCTANOIC ACID

114781-19-0: (S)-2-Amino-2-ethyloctanoic acid, also known as a branched-chain amino acid, is characterized by its chiral center, which imparts specific stereochemical properties. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), making it an α-amino acid. The presence of an ethyl group on the second carbon contributes to its hydrophobic nature, influencing its solubility and interaction with biological systems. It is typically found in a zwitterionic form at physiological pH, where the amino group is protonated and the carboxylic acid group is deprotonated. This compound is of interest in biochemical research and potential therapeutic applications, particularly in the context of protein synthesis and metabolic pathways. Its unique structure may also affect its role in cellular signaling and energy metabolism. As with many amino acids, it is likely to participate in various biochemical reactions, including transamination and peptide bond formation, contributing to the complexity of protein structures and functions in living organisms.

CAS 114781-19-0

(S)-2-AMINO-2-ETHYLOCTANOIC ACID

Octanoic acid, 2-amino-2-ethyl-, (2S)-

Ref: IN-DA000F7P

(2S)-2-Amino-2-ethyl-octanoic acid

Ref: 54-OR480341