Date published: 2025-9-30

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Hoechst 34580 (CAS 911004-45-0)

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Alternate Names:
N,N-Dimethyl-4-[5-(4-methyl-1-piperazinyl)[2,5′-bi-1H-benzimidazol]-2′-yl]benzenamine trihydrochloride; HOE 34580
Application:
Hoechst 34580 is Hoechst 34580 is a suitable fluorogenic substrate for esterases/lipases
CAS Number:
911004-45-0
Molecular Weight:
560.95
Molecular Formula:
C27H29N73HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Hoechst 34580 is a suitable fluorogenic substrate for esterases/lipases. The synthesis of Hoechst 34580 involves a multi-step process. It starts with the condensation of 4-nitro-N,N-dimethylaniline and 2,5-dimethoxybenzaldehyde to create a Schiff base. This compound is then reduced to yield the corresponding amine. Next, the amine is reacted with 2,5-diaminobenzoic acid to produce the desired benzimidazole derivative. This derivative is further reacted with 4-methylpiperazine to ultimately form the final product. The resulting product is purified and transformed into its trihydrochloride salt form.Hoechst 34580 is a valuable compound for research purposes. Its chemical formula is C27H32Cl3N7, with a molecular weight of 560.95 g/mol, and it typically exhibits a purity level of around 95%.


Hoechst 34580 (CAS 911004-45-0) References

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  2. Expression of RANKL in osteolytic membranes: association with fibroblastic cell markers.  |  Ramage, SC., et al. 2007. J Bone Joint Surg Am. 89: 841-8. PMID: 17403809
  3. Evaluation of an 8-color flow cytometric reference method for white blood cell differential enumeration.  |  Cherian, S., et al. 2010. Cytometry B Clin Cytom. 78: 319-28. PMID: 20533390
  4. KRAS-mutated non-small cell lung cancer cells are responsive to either co-treatment with erlotinib or gefitinib and histone deacetylase inhibitors or single treatment with lapatinib.  |  Kurtze, I., et al. 2011. Oncol Rep. 25: 1021-9. PMID: 21271222
  5. Host-guest interaction of Hoechst 34580 and Cucurbit[7]uril.  |  Lei, W., et al. 2011. Chemphyschem. 12: 2933-40. PMID: 21919182
  6. Natural antibody to apoptotic cell membranes inhibits the proinflammatory properties of lupus autoantibody immune complexes.  |  Vas, J., et al. 2012. Arthritis Rheum. 64: 3388-98. PMID: 22577035
  7. Peptide Anchor for Folate-Targeted Liposomal Delivery.  |  Nogueira, E., et al. 2015. Biomacromolecules. 16: 2904-10. PMID: 26241560
  8. Assessment of liposome disruption to quantify drug delivery in vitro.  |  Nogueira, E., et al. 2016. Biochim Biophys Acta. 1858: 163-7. PMID: 26589183
  9. Discovery of DNA dyes Hoechst 34580 and 33342 as good candidates for inhibiting amyloid beta formation: in silico and in vitro study.  |  Thai, NQ., et al. 2016. J Comput Aided Mol Des. 30: 639-50. PMID: 27511370
  10. A fluorescence in situ staining method for investigating spores and vegetative cells of Clostridia by confocal laser scanning microscopy and structured illuminated microscopy.  |  D'Incecco, P., et al. 2018. Micron. 110: 1-9. PMID: 29689432
  11. Application of fluorescence lifetime imaging microscopy of DNA binding dyes to assess radiation-induced chromatin compaction changes.  |  Abdollahi, E., et al. 2018. Int J Mol Sci. 19: PMID: 30110966
  12. Development of a highly sensitive, quantitative, and rapid detection system for Plasmodium falciparum-infected red blood cells using a fluorescent blue-ray optical system.  |  Yamamoto, T., et al. 2019. Biosens Bioelectron. 132: 375-381. PMID: 30901727
  13. Behavioral disturbances induced by cyanobacterial oligopeptides microginin-FR1, anabaenopeptin-A and microcystin-LR are associated with neuromotoric and cytotoxic changes in Brachionus calyciflorus.  |  Bownik, A., et al. 2022. J Hazard Mater. 438: 129472. PMID: 35785735

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hoechst 34580, 5 mg

sc-396575
5 mg
$105.00

Hoechst 34580, 50 mg

sc-396575A
50 mg
$500.00