H-N-Me-D-Ala-OH.HCl, also known as N-Methyl-D-Alanine hydrochloride, is a synthetic amino acid derivative characterized by its structural features, which include a methyl group attached to the nitrogen of the alanine backbone. This compound is typically utilized in biochemical research and pharmaceutical applications due to its role as a building block in peptide synthesis and its potential as a neurotransmitter analog. The hydrochloride form indicates that it is a salt, which enhances its solubility in water, making it suitable for various laboratory applications. The presence of the D-alanine configuration suggests that it may exhibit different biological activities compared to its L-isomer, which is more common in natural proteins. As with many amino acid derivatives, it may participate in various biochemical pathways and interactions, making it of interest in studies related to neurobiology and medicinal chemistry. Proper handling and storage conditions are essential to maintain its stability and efficacy in research settings.

H-N-Me-D-Ala-OH.HCl

1155878-14-0: H-N-Me-D-Ala-OH.HCl, also known as N-Methyl-D-Alanine hydrochloride, is a synthetic amino acid derivative characterized by its structural features, which include a methyl group attached to the nitrogen of the alanine backbone. This compound is typically utilized in biochemical research and pharmaceutical applications due to its role as a building block in peptide synthesis and its potential as a neurotransmitter analog. The hydrochloride form indicates that it is a salt, which enhances its solubility in water, making it suitable for various laboratory applications. The presence of the D-alanine configuration suggests that it may exhibit different biological activities compared to its L-isomer, which is more common in natural proteins. As with many amino acid derivatives, it may participate in various biochemical pathways and interactions, making it of interest in studies related to neurobiology and medicinal chemistry. Proper handling and storage conditions are essential to maintain its stability and efficacy in research settings.

CAS 1155878-14-0

H-N-Me-D-Ala-OH.HCl

N-Me-D-Ala-OH HCl

Ref: IN-DA008XCJ

(R)-2-(Methylamino)propanoic acid hydrochloride

Ref: 10-F450570