Alloc-β-Ala-OH
Need Assistance?
  • US & Canada:
    +
  • UK: +

Alloc-β-Ala-OH

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
β−Amino Acids
Catalog number
BAT-008327
CAS number
111695-91-1
Molecular Formula
C7H11NO4
Molecular Weight
173.17
IUPAC Name
3-(prop-2-enoxycarbonylamino)propanoic acid
Synonyms
Alloc-beta-Ala-OH; Alloc beta Ala OH; 3-(Allyloxycarbonylamino)propionic acid
InChI
InChI=1S/C7H11NO4/c1-2-5-12-7(11)8-4-3-6(9)10/h2H,1,3-5H2,(H,8,11)(H,9,10)
InChI Key
CELKWISMRZJIFN-UHFFFAOYSA-N
Canonical SMILES
C=CCOC(=O)NCCC(=O)O

Alloc-β-Ala-OH, also known as N-Alloc-β-Alanine, is a derivative of the amino acid β-alanine, and has various applications in organic synthesis and biochemical research. Here are some key applications of Alloc-β-Ala-OH:

Peptide Synthesis: Alloc-β-Ala-OH serves as a protected form of β-alanine, which is a building block in peptide synthesis. It is used to introduce β-alanine into peptide chains while preventing unwanted reactions at its amino group. This protection ensures precise control during the synthesis of complex peptides, which are vital for drug development and biochemical studies.

Drug Discovery: In medicinal chemistry, Alloc-β-Ala-OH is used in the design and synthesis of peptide-based drug candidates. Its incorporation into peptide structures can enhance the stability, bioavailability, and efficacy of therapeutic peptides. By modifying and optimizing peptide sequences, researchers can develop new drugs with improved therapeutic profiles.

Bioconjugation: Alloc-β-Ala-OH is utilized in bioconjugation techniques to link biomolecules, such as peptides and proteins, to other functional groups or labels. This is essential in the development of diagnostic tools, imaging agents, and targeted therapies. Bioconjugation with Alloc-β-Ala-OH can improve the specificity and functionality of bioactive compounds.

Combinatorial Chemistry: Alloc-β-Ala-OH is employed in combinatorial chemistry for the generation of diverse compound libraries. Its use in solid-phase peptide synthesis allows for rapid and efficient assembly of large numbers of peptides with varied sequences. These libraries are screened to identify potential leads for drug development and biochemical research.

Online Inquiry
Verification code
Inquiry Basket