Date published: 2025-9-5

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Cymoxanil (CAS 57966-95-7)

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Alternate Names:
1-(2-Cyano-2-methoxyiminoacetyl)-3-ethylurea
CAS Number:
57966-95-7
Molecular Weight:
198.18
Molecular Formula:
C7H10N4O3
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Cymoxanil, a member of the benzimidazole family of fungicides, is a broad-spectrum fungicide capable of combating a wide range of fungi such as Ascochyta, Alternaria, Botrytis, Colletotrichum, Fusarium, and Pythium species. Its systemic nature allows for absorption by plants and distribution throughout their tissues. In addition, Cymoxanil serves as a seed dressing and soil treatment to safeguard crops against fungal infections. It is widely employed in research to investigate the impact of fungal diseases on plant growth, development, and yield, as well as to assess fungicide efficacy and the resistance mechanisms of fungal pathogens.


Cymoxanil (CAS 57966-95-7) References

  1. Kinetics and mechanism of cymoxanil degradation in buffer solutions.  |  Morrica, P., et al. 2004. J Agric Food Chem. 52: 99-104. PMID: 14709020
  2. Characterization of metabolites of fungicidal cymoxanil in a sensitive strain of Botrytis cinerea.  |  Tellier, F., et al. 2008. J Agric Food Chem. 56: 8050-7. PMID: 18693740
  3. Metabolism of fungicidal cyanooximes, cymoxanil and analogues in various strains of Botrytis cinerea.  |  Tellier, F., et al. 2009. Pest Manag Sci. 65: 129-36. PMID: 18951412
  4. Toxicity of metalaxyl, azoxystrobin, dimethomorph, cymoxanil, zoxamide and mancozeb to Phytophthora infestans isolates from Serbia.  |  Rekanović, E., et al. 2012. J Environ Sci Health B. 47: 403-9. PMID: 22424065
  5. Dissipation and residue of metalaxyl and cymoxanil in pepper and soil.  |  Liu, X., et al. 2014. Environ Monit Assess. 186: 5307-13. PMID: 24791955
  6. Sensitivity to cymoxanil in Italian populations of Plasmopara viticola oospores.  |  Toffolatti, SL., et al. 2015. Pest Manag Sci. 71: 1182-8. PMID: 25212392
  7. Residue dissipation and processing factor for dimethomorph, famoxadone and cymoxanil during raisin preparation.  |  Shabeer T P, A., et al. 2015. Food Chem. 170: 180-5. PMID: 25306333
  8. Effect of different rates of spent mushroom substrate on the dissipation and bioavailability of cymoxanil and tebuconazole in an agricultural soil.  |  Álvarez-Martín, A., et al. 2016. Sci Total Environ. 550: 495-503. PMID: 26845185
  9. Residue behavior and risk assessment of cymoxanil in grape under field conditions and survey of market samples in Guangzhou.  |  Huang, J., et al. 2019. Environ Sci Pollut Res Int. 26: 3465-3472. PMID: 30515692
  10. Sensitivity of Populations of Phytophthora capsici from South Carolina to Mefenoxam, Dimethomorph, Zoxamide, and Cymoxanil.  |  Keinath, AP. 2007. Plant Dis. 91: 743-748. PMID: 30780484
  11. Improved analysis of propamocarb and cymoxanil for the investigation of residue behavior in two vegetables with different cultivation conditions.  |  Chen, X., et al. 2020. J Sci Food Agric. 100: 3157-3163. PMID: 32096228
  12. Biochemical and Histopathological Alterations in Different Tissues of Rats Due to Repeated Oral Dose Toxicity of Cymoxanil.  |  Ahmed, MS., et al. 2020. Animals (Basel). 10: PMID: 33255611
  13. Fabrication of Non-phospholipid Liposomal Nanocarrier for Sustained-Release of the Fungicide Cymoxanil.  |  Zhang, Z., et al. 2021. Front Mol Biosci. 8: 627817. PMID: 33859996

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cymoxanil, 100 mg

sc-239637
100 mg
$118.00