N-α-Carbamoyl-DL-alanine
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N-α-Carbamoyl-DL-alanine

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Category
DL-Amino Acids
Catalog number
BAT-005969
CAS number
77340-50-2
Molecular Formula
C4H8N2O3
Molecular Weight
132.12
N-α-Carbamoyl-DL-alanine
IUPAC Name
2-(carbamoylamino)propanoic acid
Synonyms
Carbamoyl-DL-Ala-OH; DL-2-Ureidopropionic acid
Purity
99%
Density
1.332 g/cm3
Melting Point
157 °C
Boiling Point
304.2 °C
Storage
Store at -20 °C
InChI
InChI=1S/C4H8N2O3/c1-2(3(7)8)6-4(5)9/h2H,1H3,(H,7,8)(H3,5,6,9)
InChI Key
LUSWEUMSEVLFEQ-UHFFFAOYSA-N
Canonical SMILES
CC(C(=O)O)NC(=O)N

N-α-Carbamoyl-DL-alanine (NCA), a versatile biochemical compound, finds a multitude of applications in bioscience and related fields. Here are the key applications of N-α-Carbamoyl-DL-alanine, presented with high perplexity and burstiness:

Pharmaceutical Synthesis: Serving as a fundamental building block in pharmaceutical compound synthesis, NCA's intricate chemical composition facilitates the incorporation of carbamoyl groups crucial for the development of specific classes of drugs. This attribute positions NCA as an indispensable intermediary in the pharmaceutical realm, aiding in the generation of active pharmaceutical ingredients and driving innovation in drug synthesis.

Enzyme Substrate Research: Positioned as a pivotal substrate in enzyme studies, particularly those centred on carbamate metabolism, NCA enables researchers to explore the breakdown and conversion processes guided by specific enzymes. This exploration yields invaluable insights into enzymatic pathways and mechanisms, laying the foundation for a deeper comprehension of metabolic disorders and the creation of enzyme-based diagnostic tools essential for enhancing healthcare diagnostics and treatments.

Academic Research: Widely utilized in academic environments for both educational and investigative purposes in the domains of organic chemistry and biochemistry, NCA stands as a staple compound for laboratory experiments and instructional showcases. Its simple synthesis and manipulability make it an ideal candidate for facilitating hands-on exploration of fundamental concepts in chemical reactions and compound characterization, empowering students and researchers to unlock the mysteries of chemical and biological processes.

Metal Chelation Studies: Exhibiting chelating capabilities, NCA acts as a binding agent, forming stable complexes with metal ions, a property integral to research concentrating on metal ion interactions within biological systems or environmental matrices. Through the analysis of these complexes, scientists delve into the dynamics of metal transport, toxicity, and nutrient availability across various contexts, unraveling the intricate relationships between metals and living organisms or ecosystems, and shedding light on crucial aspects of environmental and biological sciences.

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