Date published: 2025-10-4

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Quinoxyfen (CAS 124495-18-7)

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Alternate Names:
(5,7-Dichloro-4-quinolyl) (4-fluorophenyl) ether
Application:
Quinoxyfen is a protectant fungicide used to control powdery mildew
CAS Number:
124495-18-7
Purity:
≥98%
Molecular Weight:
308.13
Molecular Formula:
C15H8Cl2FNO
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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Quinoxyfen is a quinoline-based fungicide specifically designed for the control of powdery mildew in cereals and grapes. Its mechanism of action is distinct and involves the inhibition of fungal respiration at a site different from other fungicides, categorizing it as a mitochondrial electron transport inhibitor. Quinoxyfen primarily targets the complex III (cytochrome bc1 complex) in the mitochondrial electron transport chain of fungi, which is crucial for cellular energy production. By binding to this site, it disrupts electron transport, leading to a cessation of ATP production and ultimately causing fungal cell death. This mode of action is highly specific to fungi, making Quinoxyfen a valuable tool in agricultural research, particularly in studies aimed at understanding and managing fungal resistance. Its unique binding affinity and inhibition profile have also made it a subject of interest in basic biochemical research, where it is used to study the structure and function of mitochondrial complexes in various fungal species. Additionally, researchers utilize Quinoxyfen to explore the ecological impact of fungicides on non-target fungal communities, which is critical for developing sustainable agricultural practices and understanding the broader environmental consequences of fungicide use.


Quinoxyfen (CAS 124495-18-7) References

  1. Fate of quinoxyfen residues in grapes, wine, and their processing products.  |  Cabras, P., et al. 2000. J Agric Food Chem. 48: 6128-31. PMID: 11312786
  2. Quinoxyfen--resistance management and sensitivity monitoring in wheat: 1995-2000.  |  Bernhard, U., et al. 2002. Pest Manag Sci. 58: 972-4. PMID: 12233191
  3. Sensitivity of Uncinula necator to quinoxyfen: evaluation of isolates selected using a discriminatory dose screen.  |  Green, EA. and Gustafson, GD. 2006. Pest Manag Sci. 62: 492-7. PMID: 16612812
  4. Host perception and signal transduction studies in wild-type Blumeria graminis f. sp. hordei and a quinoxyfen-resistant mutant implicate quinoxyfen in the inhibition of serine esterase activity.  |  Lee, S., et al. 2008. Pest Manag Sci. 64: 544-55. PMID: 18229890
  5. Quinoxyfen perturbs signal transduction in barley powdery mildew (Blumeria graminis f.sp. hordei).  |  Wheeler, IE., et al. 2003. Mol Plant Pathol. 4: 177-86. PMID: 20569377
  6. Improved synthetic route to quinoxyfen photometabolite 2-chloro-10-fluorochromeno[2,3,4-de]quinoline.  |  Johnson, PL., et al. 2017. Pest Manag Sci. 73: 1703-1708. PMID: 28058778
  7. Assessment of quinoxyfen phototransformation pathways by liquid chromatography coupled to accurate mass spectrometry.  |  Ferri, P., et al. 2017. Anal Bioanal Chem. 409: 2981-2991. PMID: 28210755
  8. Immunochemical rapid determination of quinoxyfen, a priority hazardous pollutant.  |  Duncan, H., et al. 2018. Chemosphere. 211: 302-307. PMID: 30077110
  9. Evaluation of Quinoxyfen Resistance of Erysiphe necator (Grape Powdery Mildew) in a Single Virginia Vineyard.  |  Feng, X., et al. 2018. Plant Dis. 102: 2586-2591. PMID: 30307835
  10. In vitro interactions of two pesticides, propazine and quinoxyfen with bovine serum albumin: Spectrofluorometric and molecular docking investigations.  |  Duman, B., et al. 2023. Spectrochim Acta A Mol Biomol Spectrosc. 300: 122907. PMID: 37257323

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Quinoxyfen, 200 mg

sc-229030
200 mg
$157.00