H-Ala-OBut·HCL CAS:13404-22-3
H-Ala-OBut·HCl plays a crucial role in peptide synthesis and modification due to its ability to protect the amine group of L-alanine. This protective step allows for selective reactions with other functional groups, facilitating the precise construction of peptide sequences and enabling the study of structure-activity relationships in biologically active peptides. In the realm of drug discovery and development, H-Ala-OBut·HCl contributes to the creation of peptide-based pharmaceuticals and bioconjugates. Its role in peptide protection and subsequent deprotection processes is integral to the design and production of novel therapeutic agents with potential applications in targeted drug delivery and precision medicine. Furthermore, in biochemical research, H-Ala-OBut·HCl enables scientists to explore and manipulate the functions and interactions of peptides and proteins. By providing a means to selectively protect the amine group of L-alanine, researchers can elucidate biological processes and investigate potential targets for drug development, thereby expanding the understanding of molecular mechanisms in living organisms. When working with H-Ala-OBut·HCl, adherence to established laboratory safety protocols and handling guidelines is essential to ensure proper usage and minimize risks associated with chemical reagents. Understanding the specific reactivity and applications of H-Ala-OBut·HCl within the context of peptide synthesis and modification is imperative for conducting successful experiments and achieving desired scientific outcomes.
Composition | C7H16ClNO2 |
Assay | 99% |
Appearance | white powder |
CAS No. | 13404-22-3 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |