Date published: 2025-12-6

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Haloxyfop-methyl (CAS 69806-40-2)

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Alternate Names:
Haloxyfop-P-methyl; Haloxyfop methyl ester; Verdict
Application:
Haloxyfop-methyl is an herbicide
CAS Number:
69806-40-2
Purity:
≥95%
Molecular Weight:
375.73
Molecular Formula:
C16H13ClF3NO4
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-methyl is a specialized herbicide employed in both agriculture and horticulture to specifically target and eliminate certain grass weeds. It is particularly effective for managing grass weeds in crops like cereals, soybeans, and sunflowers, doing so without harming the crops when used as directed. The herbicide acts by disrupting the lipid biosynthesis pathway in plants, leading to their demise. Owing to its selective action against grass weeds, Haloxyfop-methyl is useful in various scientific research areas. It is used in studies focused on crop rotation, plant-pollinator relationships, agroecosystem analysis, and biodiversity conservation, helping researchers gain insights into the role of these weeds within the ecosystems being examined.


Haloxyfop-methyl (CAS 69806-40-2) References

  1. Method development and validation for total haloxyfop analysis in infant formulas and related ingredient matrices using liquid chromatography-tandem mass spectrometry.  |  Koesukwiwat, U., et al. 2018. Anal Bioanal Chem. 410: 5521-5528. PMID: 29737370
  2. Exposure to Herbicides Prime P450-Mediated Detoxification of Helicoverpa armigera against Insecticide and Fungal Toxin.  |  Sun, Z., et al. 2019. Insects. 10: PMID: 30641934
  3. Detection of herbicides in water bodies of the Samambaia River sub-basin in the Federal District and eastern Goiás.  |  Correia, NM., et al. 2020. J Environ Sci Health B. 55: 574-582. PMID: 32189560
  4. Synthesis of a magnetic sorbent and its application in extraction of different pesticides from water, fruit, and vegetable samples prior to their determination by gas chromatography-tandem mass spectrometry.  |  Yadeghari, A. and Farajzadeh, MA. 2021. J Chromatogr A. 1635: 461718. PMID: 33229005
  5. Environmental effects on efficacy of herbicides for postemergence goosegrass (Eleusine indica) control.  |  Shekoofa, A., et al. 2020. Sci Rep. 10: 20579. PMID: 33239643
  6. Residues and dietary intake risk assessments of clomazone, fomesafen, haloxyfop-methyl and its metabolite haloxyfop in spring soybean field ecosystem.  |  Liang, Y., et al. 2021. Food Chem. 360: 129921. PMID: 33991974
  7. Synthesis and application of trifluoromethylpyridines as a key structural motif in active agrochemical and pharmaceutical ingredients.  |  Tsukamoto, M., et al. 2021. J Pestic Sci. 46: 125-142. PMID: 34135675
  8. Validation of Reference Genes for Quantitative PCR in Johnsongrass (Sorghum halepense L.) under Glyphosate Stress.  |  Ulrich, MN., et al. 2021. Plants (Basel). 10: PMID: 34451600
  9. Impact of a Novel W2027L Mutation and Non-Target Site Resistance on Acetyl-CoA Carboxylase-Inhibiting Herbicides in a French Lolium multiflorum Population.  |  Kaundun, SS., et al. 2021. Genes (Basel). 12: PMID: 34828444
  10. Detection of pesticides in food products using paper-based devices by UV-induced fluorescence spectroscopy combined with molecularly imprinted polymers.  |  Vodova, M., et al. 2022. Food Chem. 380: 132141. PMID: 35101791
  11. A modified quick-easy-cheap-effective-rugged-and-safe method involving carbon nano-onions-based dispersive solid-phase extraction and dispersive liquid-liquid microextraction for pesticides from grapes.  |  Mokhtari, S., et al. 2022. J Sep Sci. 45: 3582-3593. PMID: 35964286
  12. Advancement of Phenoxypyridine as an Active Scaffold for Pesticides.  |  Liu, Y., et al. 2022. Molecules. 27: PMID: 36296394
  13. Developing an internal threshold of toxicological concern (iTTC).  |  Arnot, JA., et al. 2022. J Expo Sci Environ Epidemiol. 32: 877-884. PMID: 36347933

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Haloxyfop-methyl, 50 mg

sc-235276
50 mg
$57.00