Date published: 2025-10-21

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Trifloxystrobin (CAS 141517-21-7)

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Alternate Names:
Methyl (E)-α-methoxyimino-2-[(E)-1-(3-trifluoromethylphenyl)ethylidenaminooxymethyl]phenylacetate
Application:
Trifloxystrobin is a strobilurin class fungicide
CAS Number:
141517-21-7
Molecular Weight:
408.37
Molecular Formula:
C20H19F3N2O4
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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Trifloxystrobin is a strobilurin fungicide, part of a class of agricultural chemicals that are used for their highly effective fungicidal properties, particularly against a spectrum of fungal pathogens that affect crops. The main mechanism of action of Trifloxystrobin involves the inhibition of mitochondrial respiration in fungi by binding to the complex III at the Qo site, which is crucial in the electron transport chain. This binding disrupts the normal cellular processes, preventing the production of ATP, an essential molecule for energy transfer within the cell, thereby halting fungal growth and reproduction. In non-clinical research settings, Trifloxystrobin is extensively studied for its role in managing plant diseases and its behavior in various ecological systems. These studies often focus on its degradation in soil and water, its effect on non-target organisms, and the potential for resistance development in target fungi. Understanding these aspects helps in assessing its environmental impact and in developing strategies to mitigate resistance build-up. Additionally, Trifloxystrobin′s role in improving crop yield by protecting plants from debilitating diseases makes it a subject of agronomic studies aimed at optimizing application strategies and integrating it into comprehensive crop management programs.


Trifloxystrobin (CAS 141517-21-7) References

  1. Photoisomerization kinetics of trifloxystrobin.  |  Banerjee, K., et al. 2005. Anal Bioanal Chem. 382: 1527-33. PMID: 16021425
  2. Residues and dissipation of trifloxystrobin and its metabolite in tomatoes and soil.  |  Wang, L., et al. 2014. Environ Monit Assess. 186: 7793-9. PMID: 25086714
  3. Trifloxystrobin-induced mitophagy through mitochondrial damage in human skin keratinocytes.  |  Jang, Y., et al. 2016. J Toxicol Sci. 41: 731-737. PMID: 27853101
  4. Hormetic Effects of Trifloxystrobin on Aggressiveness of Sclerotinia sclerotiorum.  |  Di, YL., et al. 2016. Plant Dis. 100: 2113-2118. PMID: 30682995
  5. Dissipation and risk assessment of fluopyram and trifloxystrobin on onion by GC-MS/MS.  |  Sharma, N., et al. 2022. Environ Sci Pollut Res Int. 29: 80612-80623. PMID: 35723826
  6. Toxicological differences of trifloxystrobin and kresoxim-methyl on zebrafish in various levels of exposure routes, organs, cells and biochemical indicators.  |  Li, H., et al. 2022. Chemosphere. 306: 135495. PMID: 35772514
  7. Acute multiple toxic effects of Trifloxystrobin fungicide on Allium cepa L.  |  Macar, O., et al. 2022. Sci Rep. 12: 15216. PMID: 36076029
  8. Trifloxystrobin blocks the growth of Theileria parasites and is a promising drug to treat Buparvaquone resistance.  |  Villares, M., et al. 2022. Commun Biol. 5: 1253. PMID: 36380082
  9. Effects of the fungicide trifloxystrobin on the structure and function of soil bacterial community.  |  Xiao, Z., et al. 2023. Environ Toxicol Pharmacol. 99: 104104. PMID: 36893889
  10. Behavior of trifloxystrobin and propineb as combination product in tomato (Solanum lycopersicum) and their risk assessment for human health.  |  Litoriya, NS., et al. 2023. Biomed Chromatogr. e5660. PMID: 37085954

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Trifloxystrobin, 100 mg

sc-229576
100 mg
$101.00