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China Supplier DL-Valine丨CAS 516-06-3
DL-Valine is a racemic mixture of D-valine and L-valine, representing both enantiomeric forms of the branched-chain amino acid valine. It contains amino and carboxyl functional groups that make it useful in biochemical research, amino acid chemistry, and the synthesis of specialized organic compounds. With its defined composition of two stereoisomers, DL-Valine is relevant to research investigating chirality, amino acid properties, and stereochemistry-dependent chemical and biological behavior.
Chemical Identifiers
| InChI | InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8) |
| InChI Key | KZSNJWFQEVHDMF-UHFFFAOYSA-N |
| Smiles | CC(C)C(C(=O)O)N |
| EC No. | 208-220-0 |
| MDL No. | MFCD00004267 |
| PubChem CID | 1182 |
Applications
Pharmaceutical Research and Drug Discovery
Amino acids are important building blocks in pharmaceutical research and medicinal chemistry. DL-Valine may serve as a starting material for selected synthetic investigations involving amino acid derivatives and chiral compounds. Researchers can use it to explore stereochemical effects and develop functionalized intermediates, with the suitability of the racemic mixture determined by the target molecule and synthetic strategy.
Biochemical and Metabolic Research
Valine is one of the branched-chain amino acids studied in protein metabolism and biochemical pathways. DL-Valine can be used in laboratory research examining amino acid stereochemistry, enzyme selectivity, and differences in the behavior of D- and L-amino acids. Its application depends on the experimental model and whether a racemic mixture is appropriate for the intended study.
Chiral Synthesis and Amino Acid Derivatives
Peptide Chemistry and Molecular Design
Valine derivatives are relevant to peptide synthesis and the investigation of amino acid sequence–structure relationships. DL-Valine may support research comparing the effects of different amino acid configurations on molecular conformation and reactivity. Because peptide synthesis often requires a specific stereochemical configuration, the D- and L-components should be considered separately when a defined enantiomer is needed.
