Date published: 2026-4-25

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Nitrofurantoin (CAS 67-20-9)

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Application:
Nitrofurantoin is a nitrofuran antibiotic
CAS Number:
67-20-9
Molecular Weight:
238.16
Molecular Formula:
C8H6N4O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Nitrofurantoin, identified by the CAS number 67-20-9, is a nitrofuran derivative extensively used in scientific studies focusing on bacterial biochemistry and genetics. The core mechanism of action of Nitrofurantoin involves the disruption of bacterial enzymatic processes through the chemical reduction of its nitro group, which leads to the formation of reactive intermediates. These intermediates are capable of altering bacterial ribosomal proteins and DNA, thus inhibiting vital cellular functions such as protein synthesis and DNA replication. In research environments, Nitrofurantoin has been employed to study the bacterial response to oxidative stress and the genetic pathways involved in resistance to redox-active compounds. This compound is particularly useful for its broad spectrum of activity, allowing researchers to examine its effects across a variety of bacterial species, including both Gram-positive and Gram-negative organisms. Studies utilizing Nitrofurantoin have also focused on elucidating the mechanisms by which bacteria activate and deactivate the compound, shedding light on microbial metabolic pathways. Furthermore, research involving Nitrofurantoin has contributed significantly to understanding the cellular targets of redox-cycling agents, providing insights that are vital for the development of novel strategies to control bacterial populations in both environmental and industrial settings.


Nitrofurantoin (CAS 67-20-9) References

  1. Evaluation of nitrofurantoin combination therapy of metronidazole-sensitive and -resistant Helicobacter pylori infections in mice.  |  Jenks, PJ., et al. 2000. Antimicrob Agents Chemother. 44: 2623-9. PMID: 10991835
  2. Organ-targeted mutagenicity of nitrofurantoin in Big Blue transgenic mice.  |  Quillardet, P., et al. 2006. Mutagenesis. 21: 305-11. PMID: 16895946
  3. Effect of pregnancy on nitrofurantoin disposition in mice.  |  Zhang, Y., et al. 2009. J Pharm Sci. 98: 4306-15. PMID: 19422048
  4. Differential effects of chrysin on nitrofurantoin pharmacokinetics mediated by intestinal breast cancer resistance protein in rats and mice.  |  Kawase, A., et al. 2009. J Pharm Pharm Sci. 12: 150-63. PMID: 19732493
  5. Prostatic inflammation induces urinary frequency in adult mice.  |  Lee, S., et al. 2015. PLoS One. 10: e0116827. PMID: 25647072
  6. Role of oxidative stress in the chemical structure-related genotoxicity of nitrofurantoin in Nrf2-deficient gpt delta mice.  |  Tsuchiya, T., et al. 2018. J Toxicol Pathol. 31: 169-178. PMID: 30093786
  7. Therapeutic Efficacy of Orally Administered Nitrofurantoin against Animal African Trypanosomosis Caused by Trypanosoma congolense Infection.  |  Suganuma, K., et al. 2022. Pathogens. 11: PMID: 35335655
  8. Composite of a Stabilizer-Free Trimetallic Prussian Blue Analogue (PBA) and Polyaniline (PANI) on 3D Porous Nickel Foam for the Detection of Nitrofurantoin in Biological Fluids.  |  Mukundan, G. and Badhulika, S. 2024. ACS Appl Bio Mater. 7: 2924-2935. PMID: 38637912
  9. Nitrofurantoin-induced hepatic and pulmonary biochemical changes in mice fed different vitamin E doses.  |  Adam, A., et al. 1996. Pharmacol Toxicol. 79: 334-9. PMID: 9000262

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Nitrofurantoin, 10 g

sc-212399
10 g
$84.00