Date published: 2025-12-4

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Nitrofurazone (CAS 59-87-0)

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Alternate Names:
2-[(5-Nitro-2-furanyl)methylene]hydrazinecarboxamide; (5-Nitro-2-furfurylidenamino)urea; 1-(5-Nitro-2-furfurylidene)semicarbazide; Aldomycin; Alfucin; Amifur; Babrocid; Chemofuran; Coxistat; Furesol; Mammex; Mastofuran; Nitrozone; Otofural; Vabrocid
Application:
Nitrofurazone is an anti-infective and an antimicrobial
CAS Number:
59-87-0
Purity:
≥98%
Molecular Weight:
198.14
Molecular Formula:
C6H6N4O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Nitrofurazone, a nitrofuran derivative, has garnered significant attention in scientific research due to its broad-spectrum antimicrobial properties and diverse applications. Its mechanism of action primarily involves the disruption of bacterial cell metabolism and DNA synthesis. Nitrofurazone is converted into reactive intermediates within bacterial cells, which subsequently interact with cellular macromolecules, including proteins and nucleic acids. This interaction leads to the inhibition of key enzymes involved in bacterial metabolism and DNA replication, ultimately resulting in bacterial cell death. Research has explored the efficacy of nitrofurazone against various bacterial pathogens, including both Gram-positive and Gram-negative bacteria, as well as some protozoa. Furthermore, studies have investigated its potential for use in agricultural settings as a veterinary disinfectant and as an antimicrobial agent in aquaculture. Additionally, nitrofurazone has been examined for its wound-healing properties, with research focusing on its ability to promote tissue regeneration and reduce bacterial colonization in injured tissues. Overall, the versatile antimicrobial activity of nitrofurazone continues to drive ongoing research efforts aimed at exploring its potential applications across diverse fields.


Nitrofurazone (CAS 59-87-0) References

  1. Nitrofurazone Removal from Water Enhanced by Coupling Photocatalysis and Biodegradation.  |  Smułek, W., et al. 2021. Int J Mol Sci. 22: PMID: 33671749
  2. Nitrofurazone repurposing towards design and synthesis of novel apoptotic-dependent anticancer and antimicrobial agents: Biological evaluation, kinetic studies and molecular modeling.  |  El-Wakil, MH., et al. 2021. Bioorg Chem. 113: 104971. PMID: 34051413
  3. Furacin: More than just contact dermatitis from nitrofurazone.  |  Cuevas Bravo, C., et al. 2021. Ann Allergy Asthma Immunol. 127: 389-390. PMID: 34087479
  4. A community-based approach to analyzing the ecotoxicity of nitrofurazone using periphytic protozoa.  |  Kazmi, SSUH., et al. 2022. Mar Pollut Bull. 175: 113165. PMID: 34839952
  5. Insights into the ecotoxicity of nitrofurazone in marine ecosystems based on body-size spectra of periphytic ciliates.  |  Kazmi, SSUH., et al. 2022. Mar Pollut Bull. 174: 113217. PMID: 34864466
  6. Electrochemical sensing of nitrofurazone on Ru(bpy)32+ functionalized polyoxometalate combined with graphene modified electrode.  |  Cai, S., et al. 2022. Food Chem. 378: 132084. PMID: 35030464
  7. Effects of nitrofurazone on ecosystem function in marine environments: A case study on microbial fauna.  |  Uroosa, ., et al. 2022. Mar Pollut Bull. 184: 114216. PMID: 36215761
  8. Antibiotic nitrofurazone drives the functional dynamics of periphytic protozoan fauna in marine environments.  |  Kazmi, SSUH., et al. 2023. Sci Total Environ. 874: 162405. PMID: 36858212
  9. Research progress on metabolites of nitrofurazone in aquatic products.  |  Yang, G., et al. 2024. Heliyon. 10: e29735. PMID: 38681547

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Nitrofurazone, 100 mg

sc-212400
100 mg
$87.00

Nitrofurazone, 100 g

sc-212400A
100 g
$126.00