Date published: 2026-5-10

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Ethalfluralin (CAS 55283-68-6)

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Alternate Names:
Sonalan
CAS Number:
55283-68-6
Molecular Weight:
333.26
Molecular Formula:
C13H14F3N3O4
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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Ethalfluralin, known as EFL, is a synthetic herbicide widely used in agriculture, lawn care, and various commercial applications. Belonging to the family of cyclohexanedione herbicides, it effectively controls weeds in crops such as corn, soybeans, and cotton. Its mode of action involves inhibiting cell division and growth in plants, leading to their demise. Remarkably, Ethalfluralin has maintained its popularity over the last three decades, making it one of the most extensively used herbicides globally. In scientific circles, Ethalfluralin has been the subject of extensive research. It serves as a model compound for studying the mechanism of action of other herbicides and understanding their impact on plant growth and development. Additionally, Ethalfluralin′s effects on soil microbial communities and aquatic ecosystems have been carefully investigated. The herbicidal prowess of Ethalfluralin is attributed to its binding with acetolactate synthase (ALS), an enzyme for the synthesis of branched-chain amino acids in plants. By attaching to ALS, Ethalfluralin disrupts the formation of these essential amino acids, hampering plant growth. Consequently, this inhibition of cell division and growth leads to the eventual death of the targeted plants.


Ethalfluralin (CAS 55283-68-6) References

  1. Determination of ethalfluralin in canola seed, meal, and refined oil by capillary gas chromatography with mass selective detection.  |  Shackelford, DD., et al. 2000. J Agric Food Chem. 48: 4422-7. PMID: 10995373
  2. Foliar and soil deposition of pesticide sprays in peanuts and their washoff and runoff under simulated worst-case rainfall conditions.  |  Wauchope, RD., et al. 2004. J Agric Food Chem. 52: 7056-63. PMID: 15537318
  3. Study of the voltammetric behaviour of the ethalfluralin and methalpropalin and its determination in environmental matrices at hanging mercury drop electrode.  |  Thriveni, T., et al. 2009. Environ Monit Assess. 151: 9-18. PMID: 18386143
  4. Development of a multiresidue method for the determination of multiclass pesticides in soil using GC.  |  Park, JH., et al. 2010. Biomed Chromatogr. 24: 893-901. PMID: 20039336
  5. Enhanced dissipation of oxyfluorfen, ethalfluralin, trifluralin, propyzamide, and pendimethalin in soil by solarization and biosolarization.  |  Fenoll Serrano, J., et al. 2010. J Agric Food Chem. 58: 2433-8. PMID: 20112907
  6. Development of a gas chromatography-mass spectrometry method for the determination of pesticides in gaseous and particulate phases in the atmosphere.  |  Borrás, E., et al. 2011. Anal Chim Acta. 699: 57-65. PMID: 21704758
  7. Gas-phase degradation of the herbicide ethalfluralin under atmospheric conditions.  |  Muñoz, A., et al. 2014. Chemosphere. 95: 395-401. PMID: 24139158
  8. Pesticide residue concentration in soil following conventional and Low-Input Crop Management in a Mediterranean agro-ecosystem, in Central Greece.  |  Karasali, H., et al. 2016. Sci Total Environ. 541: 130-142. PMID: 26406107
  9. Dinitroaniline herbicide resistance in a multiple-resistant Lolium rigidum population.  |  Chen, J., et al. 2018. Pest Manag Sci. 74: 925-932. PMID: 29148165
  10. Screening of multiclass pesticide residues in honey by SPE-GC/MSD: a pilot study.  |  Rafique, N., et al. 2018. Environ Monit Assess. 190: 666. PMID: 30350126
  11. Gas chromatographic determination of residue levels of the herbicides trifluralin, benefin, ethalfluralin, and isopropalin in soil with confirmation by mass selective detection.  |  West, SD., et al. 1988. J Assoc Off Anal Chem. 71: 1082-5. PMID: 3240956
  12. Ethalfluralin impairs implantation by aggravation of mitochondrial viability and function during early pregnancy.  |  Ham, J., et al. 2022. Environ Pollut. 307: 119495. PMID: 35605831
  13. Ethalfluralin induces developmental toxicity in zebrafish via oxidative stress and inflammation.  |  Hong, T., et al. 2022. Sci Total Environ. 854: 158780. PMID: 36115403
  14. Comparison of the persistence of ethalfluralin and trifluralin in Saskatchewan field soils.  |  Hayden, BJ. and Smith, AE. 1980. Bull Environ Contam Toxicol. 25: 508-11. PMID: 7426803
  15. Inhibition of Toxoplasma gondii replication by dinitroaniline herbicides.  |  Stokkermans, TJ., et al. 1996. Exp Parasitol. 84: 355-70. PMID: 8948325

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ethalfluralin, 250 mg

sc-252787
250 mg
$32.00