DL-Aspartic acid b-methyl ester hydrochloride
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DL-Aspartic acid b-methyl ester hydrochloride

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Category
DL-Amino Acids
Catalog number
BAT-003583
CAS number
1835-52-5
Molecular Formula
C5H9NO4·HCl
Molecular Weight
183.64
DL-Aspartic acid b-methyl ester hydrochloride
IUPAC Name
2-amino-4-methoxy-4-oxobutanoic acid;hydrochloride
Synonyms
DL-Asp(OMe)-OH HCl; 2-amino-4-methoxy-4-oxobutanoic acid hydrochloride; beta-Methyl L-aspartate hydrochloride; H-D-Asp(OMe)-OH HCl
Appearance
White powder
Purity
≥ 98% (HPLC)
Melting Point
196-200 °C
Storage
Store at 2-8°C
InChI
InChI=1S/C5H9NO4.ClH/c1-10-4(7)2-3(6)5(8)9;/h3H,2,6H2,1H3,(H,8,9);1H
InChI Key
QRBMPUYOGOCYDJ-UHFFFAOYSA-N
Canonical SMILES
COC(=O)CC(C(=O)O)N.Cl

DL-Aspartic acid β-methyl ester hydrochloride, a derivative of aspartic acid widely utilized in biochemical and pharmaceutical research, offers a myriad of applications. Here are four key applications presented with high perplexity and burstiness:

Peptide Synthesis: Serving as a fundamental component in the synthesis of peptides and proteins, DL-Aspartic acid β-methyl ester hydrochloride plays a crucial role in peptide assembly. Its ester form provides protection to functional groups during peptide coupling reactions, ensuring enhanced yield and purity in the generation of synthetic peptides utilized in both research and therapeutic contexts.

Neurobiology Research: In the realm of neurobiology, this compound emerges as a pivotal tool for exploring neurotransmitter systems and synaptic functionalities. As a derivative of aspartic acid, it allows researchers to delve into the involvement of excitatory amino acids in the intricate workings of the central nervous system.

Metabolic Studies: Within the domain of metabolic research, DL-Aspartic acid β-methyl ester hydrochloride stands out as a valuable asset for studying amino acid metabolism and biosynthetic pathways. Its integration into metabolic investigations aids in deciphering how cells metabolize and utilize diverse amino acids, thereby enriching our understanding of metabolic diseases and informing potential strategies for intervention.

Pharmaceutical Development: Harnessing its versatility, this compound finds extensive utility in pharmaceutical research as an intermediate for formulating novel drug candidates. Its unique properties make it amenable to chemical modifications and integration into complex molecular structures, facilitating the synthesis of innovative therapeutics targeting a spectrum of medical conditions and underscoring its role in advancing pharmaceutical innovation.

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