L-Proline, 4-amino-1-methyl-, methyl ester, hydrochloride (1:2), (4S)- is a derivative of proline, an amino acid that plays a crucial role in protein synthesis and is involved in various metabolic processes. This compound features a methyl ester functional group, which enhances its solubility and bioavailability. The hydrochloride form indicates that it is a salt, which typically improves stability and handling properties. As a chiral molecule, it exists in a specific stereoisomeric form, denoted as (4S)-, which is significant in biological systems where chirality can influence activity and interactions. The compound is likely to exhibit characteristics typical of amino acids and their derivatives, such as being hygroscopic and soluble in water and polar solvents. Its applications may extend to pharmaceuticals, biochemistry, and research, particularly in studies involving peptide synthesis or as a building block in drug development. Safety and handling precautions should be observed, as with any chemical substance, particularly in laboratory settings.

<span class="text-smallcaps">L</span>-Proline, 4-amino-1-methyl-, methyl ester, hydrochloride (1:2), (4S)-

1300698-39-8: L-Proline, 4-amino-1-methyl-, methyl ester, hydrochloride (1:2), (4S)- is a derivative of proline, an amino acid that plays a crucial role in protein synthesis and is involved in various metabolic processes. This compound features a methyl ester functional group, which enhances its solubility and bioavailability. The hydrochloride form indicates that it is a salt, which typically improves stability and handling properties. As a chiral molecule, it exists in a specific stereoisomeric form, denoted as (4S)-, which is significant in biological systems where chirality can influence activity and interactions. The compound is likely to exhibit characteristics typical of amino acids and their derivatives, such as being hygroscopic and soluble in water and polar solvents. Its applications may extend to pharmaceuticals, biochemistry, and research, particularly in studies involving peptide synthesis or as a building block in drug development. Safety and handling precautions should be observed, as with any chemical substance, particularly in laboratory settings.

CAS 1300698-39-8

<span class="text-smallcaps">L</span>-Proline, 4-amino-1-methyl-, methyl ester, hydrochloride (1:2), (4S)-

Methyl-(4S)-4-amino-1-methyl-L-prolinate dihydrochloride

Ref: 10-F063177