N-(2-hydroxyethyl)-L-valine, with the CAS number 101769-73-7, is an amino acid derivative characterized by the presence of a hydroxyethyl group attached to the nitrogen of the valine side chain. This compound is a non-essential amino acid, which means it can be synthesized by the body. It exhibits properties typical of amino acids, including the ability to participate in peptide bond formation and serve as a building block for proteins. The hydroxyethyl group introduces additional hydrophilicity, potentially enhancing its solubility in aqueous environments. This modification can also influence its biological activity and interactions with other biomolecules. N-(2-hydroxyethyl)-L-valine may be utilized in various biochemical applications, including as a chiral building block in pharmaceutical synthesis or as a component in peptide synthesis. Its structural features may also allow it to play a role in drug formulation or as a stabilizing agent in certain biochemical processes. Overall, this compound's unique characteristics make it of interest in both research and industrial applications.

N-(2-hydroxyethyl)-L-valine

101769-73-7: N-(2-hydroxyethyl)-L-valine, with the CAS number 101769-73-7, is an amino acid derivative characterized by the presence of a hydroxyethyl group attached to the nitrogen of the valine side chain. This compound is a non-essential amino acid, which means it can be synthesized by the body. It exhibits properties typical of amino acids, including the ability to participate in peptide bond formation and serve as a building block for proteins. The hydroxyethyl group introduces additional hydrophilicity, potentially enhancing its solubility in aqueous environments. This modification can also influence its biological activity and interactions with other biomolecules. N-(2-hydroxyethyl)-L-valine may be utilized in various biochemical applications, including as a chiral building block in pharmaceutical synthesis or as a component in peptide synthesis. Its structural features may also allow it to play a role in drug formulation or as a stabilizing agent in certain biochemical processes. Overall, this compound's unique characteristics make it of interest in both research and industrial applications.

<p>Applications Cotinine and N-(2-hydroxyethyl)valine are markers of passive exposure to tobacco smoke in children.<br>References Dempsey, D., et al.: Clin. Pharmacol. Ther., 67, 458 (2000), Smith, C., et al.: Food Chem. Toxicol., 41, 807 (20030,<br></p>

CAS 101769-73-7

N-(2-hydroxyethyl)-L-valine

N-2-(Hydroxyethyl)-L-valine

Ref: TR-H942300