Date published: 2025-11-1

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Fmoc-Ala-Ala-OH (CAS 87512-31-0)

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Alternate Names:
Fmoc-L-alanyl-L-alanine
Application:
Fmoc-Ala-Ala-OH is an Fmoc protected alanine derivative
CAS Number:
87512-31-0
Purity:
≥98%
Molecular Weight:
382.41
Molecular Formula:
C21H22N2O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Fmoc-Ala-Ala-OH is a dipeptide derivative used as a building block in peptide synthesis. It functions as a protecting group for the amino group of the N-terminal amino acid, allowing for selective deprotection and subsequent coupling reactions. Fmoc-Ala-Ala-Oh plays a role in solid-phase peptide synthesis by facilitating the stepwise elongation of peptide chains. Its mechanism of action involves the temporary masking of the N-terminal amino group, preventing unwanted side reactions during the peptide assembly process. Fmoc-Ala-Ala-OH interacts at the molecular level by forming stable amide bonds with the carboxyl group of the C-terminal amino acid, enabling the controlled and sequential addition of amino acids to the growing peptide chain.


Fmoc-Ala-Ala-OH (CAS 87512-31-0) References

  1. Identification of Fmoc-beta-Ala-OH and Fmoc-beta-Ala-amino acid-OH as new impurities in Fmoc-protected amino acid derivatives.  |  Hlebowicz, E., et al. 2005. J Pept Res. 65: 90-7. PMID: 15686539
  2. Covalent Structure and Bioactivity of the Type AII Lantibiotic Salivaricin A2.  |  Geng, M., et al. 2018. Appl Environ Microbiol. 84: PMID: 29269497
  3. A General Method to Prepare Peptide-Based Supramolecular Hydrogels.  |  Yuan, D., et al. 2018. Methods Mol Biol. 1777: 175-180. PMID: 29744834
  4. Programmed assembly of synthetic protocells into thermoresponsive prototissues.  |  Gobbo, P., et al. 2018. Nat Mater. 17: 1145-1153. PMID: 30297813
  5. Oscillating the local milieu of polymersome interiors via single input-regulated bilayer crosslinking and permeability tuning.  |  Liu, G., et al. 2022. Nat Commun. 13: 585. PMID: 35102153
  6. Cyanoacetamide-based oxime carbonates: an efficient, simple alternative for the introduction of Fmoc with minimal dipeptide formation  |  Khattab, S. N., Subirós-Funosas, R., El-Faham, A., & Albericio, F. 2012. Tetrahedron. 68(14): 3056-3062.
  7. Extending the pool of compatible peptide hydrogels for protein crystallization  |  Escolano-Casado, G., Contreras-Montoya, R., Conejero-Muriel, M., Castellví, A., Juanhuix, J., Lopez-Lopez, M. T.,.. & Gavira, J. A. 2019. Crystals. 9(5): 244.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Fmoc-Ala-Ala-OH, 1 g

sc-294775
1 g
$300.00

Fmoc-Ala-Ala-OH, 5 g

sc-294775A
5 g
$1060.00