Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of dl-alanine丨cas 302-72-7 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.
Quality Supplier DL-Alanine丨CAS 302-72-7
DL-Alanine is a racemic mixture of D-alanine and L-alanine, containing equal proportions of the two stereoisomeric forms of this simple amino acid. Its molecular structure features an amino group, a carboxyl group, and a methyl side chain, making it a useful compound in amino acid chemistry, biochemical research, and organic synthesis. Its defined racemic composition makes DL-Alanine relevant to studies of chirality, enzyme selectivity, and the chemical properties of amino acids.
Chemical Identifiers
| InChI | InChI=1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6) |
| InChI Key | QNAYBMKLOCPYGJ-UHFFFAOYSA-N |
| Smiles | CC(C(=O)O)N |
| EC No. | 206-126-4 |
| MDL No. | MFCD00064408 |
| PubChem CID | 602 |
Applications
Pharmaceutical Research and Drug Discovery
Amino acids are important starting materials in medicinal chemistry and pharmaceutical intermediate development. DL-Alanine may serve as a building block for selected synthetic routes involving amino acid derivatives and functionalized organic compounds. Its racemic composition can also be useful in comparative research investigating the influence of stereochemistry on molecular properties and biological activity.
Biochemical and Metabolic Research
Alanine is involved in amino acid metabolism and the transfer of nitrogen and carbon between metabolic pathways. DL-Alanine can be used in laboratory studies investigating amino acid stereochemistry, enzyme specificity, and differences in the behavior of D- and L-amino acids. Researchers can use it to examine how stereochemical configuration influences interactions with biological systems.
Chiral Synthesis and Amino Acid Derivatives
Peptide Chemistry and Molecular Design
Alanine is frequently used in peptide research because its small side chain provides a useful reference for investigating peptide structure and conformation. DL-Alanine may support studies comparing the effects of D- and L-amino acid configurations on molecular behavior and synthetic outcomes. For peptide synthesis requiring a specific stereochemical sequence, the appropriate individual enantiomer should be selected rather than the racemic mixture.
