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Haloxyfop (CAS 69806-34-4)

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Alternate Names:
2-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]propanoic acid
Application:
Haloxyfop is a control for the compounds haloxyfop-methyl or haloxyfop-P-methyl
CAS Number:
69806-34-4
Molecular Weight:
361.70
Molecular Formula:
C15H11ClF3NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Haloxyfop is a chemical compound that is primarily used in agricultural research focused on the study of herbicidal action, particularly in the control of grassy weeds. Researchers investigate the mechanisms by which haloxyfop acts as a post-emergence herbicide, often exploring its inhibition of fatty acid synthesis in target plant species. This inhibition leads to the disruption of cell membrane formation and plant growth. The compound′s selectivity and effectiveness in various crop systems are key areas of study, aiming to optimize weed management practices while minimizing impacts on non-target species. Additionally, research on haloxyfop includes environmental fate studies, where its persistence, degradation, and movement within ecosystems are monitored to ensure responsible usage and to inform regulatory decisions.


Haloxyfop (CAS 69806-34-4) References

  1. Molecular basis for the inhibition of the carboxyltransferase domain of acetyl-coenzyme-A carboxylase by haloxyfop and diclofop.  |  Zhang, H., et al. 2004. Proc Natl Acad Sci U S A. 101: 5910-5. PMID: 15079078
  2. Inhibition of Acetyl-CoA Carboxylase Activity by Haloxyfop and Tralkoxydim.  |  Secor, J. and Cséke, C. 1988. Plant Physiol. 86: 10-2. PMID: 16665846
  3. Haloxyfop Inhibition of the Pyruvate and the alpha-Ketoglutarate Dehydrogenase Complexes of Corn (Zea mays L.) and Soybean (Glycine max [L.] Merr.).  |  Cho, HY., et al. 1988. Plant Physiol. 87: 334-40. PMID: 16666143
  4. A different mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by tepraloxydim.  |  Xiang, S., et al. 2009. Proc Natl Acad Sci U S A. 106: 20723-7. PMID: 19926852
  5. Trypanosoma brucei: inhibition of acetyl-CoA carboxylase by haloxyfop.  |  Vigueira, PA. and Paul, KS. 2012. Exp Parasitol. 130: 159-65. PMID: 22119241
  6. Allelic mutations in acetyl-coenzyme A carboxylase confer herbicide tolerance in maize.  |  Marshall, LC., et al. 1992. Theor Appl Genet. 83: 435-42. PMID: 24202589
  7. Stereoselective quantitation of haloxyfop in environment samples and enantioselective degradation in soils.  |  Sun, M., et al. 2015. Chemosphere. 119: 583-589. PMID: 25128890
  8. Inhibition of plant acetyl-coenzyme A carboxylase by the herbicides sethoxydim and haloxyfop.  |  Burton, JD., et al. 1987. Biochem Biophys Res Commun. 148: 1039-44. PMID: 2891354
  9. Unravelling the binding affinity between model transport protein and a prospective tuberculosis therapeutic agent: a spectroscopic and theoretical simulation exploration.  |  Wang, L., et al. 2019. J Biomol Struct Dyn. 37: 4507-4521. PMID: 30663540
  10. Molecular characteristics of the first case of haloxyfop-resistant Poa annua.  |  Ghanizadeh, H., et al. 2020. Sci Rep. 10: 4231. PMID: 32144361
  11. Haloxyfop determination by gas chromatography/tandem mass spectrometry in eggs.  |  Lehner, AF., et al. 2020. Rapid Commun Mass Spectrom. 34: e8895. PMID: 32662916
  12. Toxicity of the herbicides diuron, propazine, tebuthiuron, and haloxyfop to the diatom Chaetoceros muelleri.  |  Thomas, MC., et al. 2020. Sci Rep. 10: 19592. PMID: 33177549
  13. Species-dependent induction of peroxisome proliferation by haloxyfop, an aryloxyphenoxy herbicide.  |  Stott, WT., et al. 1995. Fundam Appl Toxicol. 28: 71-9. PMID: 8566486

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Haloxyfop, 100 mg

sc-235275
100 mg
$109.00