Date published: 2026-6-5

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5-Aminobenzimidazole (CAS 934-22-5)

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Alternate Names:
6-Aminobenzimidazole
CAS Number:
934-22-5
Purity:
>99%
Molecular Weight:
133.15
Molecular Formula:
C7H7N3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-Aminobenzimidazole is an organic compound that belongs to the benzimidazole family. It is a heterocyclic aromatic compound. 5-aminobenzimidazole serves as a key building block in the development of dyes and pigments, where its ability to form stable, conjugated systems can be utilized to produce compounds with desirable color properties. Its application in agrochemicals includes the synthesis of compounds that can function as growth regulators or pesticides. It participates in a wide range of chemical reactions, including nucleophilic substitution and coupling reactions, which are fundamental in the construction of more complex molecules.


5-Aminobenzimidazole (CAS 934-22-5) References

  1. 5-Aminobenzimidazole as new hydrophobic charge-induction ligand for expanded bed adsorption of bovine IgG.  |  Shi, W., et al. 2015. J Chromatogr A. 1425: 97-105. PMID: 26585208
  2. Poly(glycidyl methacrylate)-grafted hydrophobic charge-induction agarose resins with 5-aminobenzimidazole as a functional ligand.  |  Liu, T., et al. 2016. J Sep Sci. 39: 3130-6. PMID: 27465269
  3. Selectivity evaluation and separation of human immunoglobulin G, Fab and Fc fragments with mixed-mode resins.  |  Luo, YD., et al. 2017. J Chromatogr B Analyt Technol Biomed Life Sci. 1040: 105-111. PMID: 27978464
  4. Evaluation of adsorption selectivity of immunoglobulins M, A and G and purification of immunoglobulin M with mixed-mode resins.  |  Luo, YD., et al. 2018. J Chromatogr A. 1533: 77-86. PMID: 29241957
  5. 5-Aminobenzimidazole inhibits gastric acid secretion in Shay-rats.  |  Trivulzio, S., et al. 1988. Pharmacol Res Commun. 20: 975-82. PMID: 3241822
  6. Identification of Quinazolinone Analogs Targeting CDK5 Kinase Activity and Glioblastoma Cell Proliferation.  |  Peyressatre, M., et al. 2020. Front Chem. 8: 691. PMID: 32974274
  7. Reactional Processes on Osmium-Polymeric Membranes for 5-Nitrobenzimidazole Reduction.  |  Nechifor, AC., et al. 2021. Membranes (Basel). 11: PMID: 34436396
  8. Post-Synthetic Modification of a Metal-Organic Framework Glass.  |  Bumstead, AM., et al. 2022. Chem Mater. 34: 2187-2196. PMID: 35578693
  9. Low-Temperature Curable Negative-Tone Photosensitive Polyimides: Structure and Properties.  |  Fan, SN., et al. 2023. Polymers (Basel). 15: PMID: 36850257

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Aminobenzimidazole, 1 g

sc-262397
1 g
$104.00

5-Aminobenzimidazole, 2.5 g

sc-262397A
2.5 g
$235.00