Date published: 2026-2-18

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Bis-Boc-amino-oxyacetic acid (CAS 293302-31-5)

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Alternate Names:
Bis-Boc-Aoa
CAS Number:
293302-31-5
Molecular Weight:
291.30
Molecular Formula:
C12H21NO7
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Bis-Boc-amino-oxyacetic acid, is an organic compound extensively employed in diverse scientific applications. Bis-Boc-amino-oxyacetic acid finds utility in biochemistry and molecular biology as a reagent for protein modification, including antibody synthesis. it contributes to the study of enzyme kinetics, as well as enzyme inhibition and activation. While the precise mechanism of action remains incompletely understood, it is believed that the compound acts as a competitive inhibitor of enzymes and modulates protein-protein interactions. There is also a suggestion that Bis-Boc-amino-oxyacetic acid may function as an agonist or antagonist of specific receptors, although further confirmation is required.


Bis-Boc-amino-oxyacetic acid (CAS 293302-31-5) References

  1. Synthesis of p-(di-tert-butyl[(18)F]fluorosilyl)benzaldehyde ([(18)F]SiFA-A) with high specific activity by isotopic exchange: a convenient labeling synthon for the (18)F-labeling of N-amino-oxy derivatized peptides.  |  Schirrmacher, E., et al. 2007. Bioconjug Chem. 18: 2085-9. PMID: 18030993
  2. Glycation methods for bombesin analogs containing the (NalphaHis)Ac chelator for 99mTc(CO)3 radiolabeling.  |  Brans, L., et al. 2008. Chem Biol Drug Des. 72: 496-506. PMID: 19016795
  3. Anhydrotetracycline-peptide conjugates as representatives for ligand-based transactivating systems.  |  Lochner, S., et al. 2010. Bioorg Med Chem. 18: 6127-33. PMID: 20638851
  4. Combined effect of osteopontin and BMP-2 derived peptides grafted to an adhesive hydrogel on osteogenic and vasculogenic differentiation of marrow stromal cells.  |  He, X., et al. 2012. Langmuir. 28: 5387-97. PMID: 22372823
  5. Versatile C(3)-symmetric scaffolds and their use for covalent stabilization of the foldon trimer.  |  Berthelmann, A., et al. 2014. Org Biomol Chem. 12: 2606-14. PMID: 24637609
  6. Synthesis of relaxin-2 and insulin-like peptide 5 enabled by novel tethering and traceless chemical excision.  |  Thalluri, K., et al. 2017. J Pept Sci. 23: 455-465. PMID: 28466571

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Bis-Boc-amino-oxyacetic acid, 250 mg

sc-475964
250 mg
$86.00

Bis-Boc-amino-oxyacetic acid, 1 g

sc-475964A
1 g
$171.00