Date published: 2026-5-22

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Furalaxyl (CAS 57646-30-7)

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Alternate Names:
Fonganil; Fongarid
CAS Number:
57646-30-7
Molecular Weight:
301.34
Molecular Formula:
C17H19NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Furalaxyl is a systemic fungicide that functions by inhibiting the biosynthesis of fatty acids in the oomycete pathogen. It targets the enzyme fatty acid synthase, which is for the production of fatty acids in the pathogen. By disrupting this process, furalaxyl interferes with the pathogen′s ability to form cell membranes and other structures, ultimately leading to its death. This mode of action makes furalaxyl effective in controlling oomycete pathogens, such as downy mildew and late blight, in various crops. Furalaxyl′s ability to target the fatty acid synthesis pathway in the pathogen makes studying the molecular mechanisms of fungal and oomycetes.


Furalaxyl (CAS 57646-30-7) References

  1. Enantioselective degradation of the chiral fungicides metalaxyl and furalaxyl by Brevibacillus brevis.  |  Sulimma, L., et al. 2013. Chirality. 25: 336-40. PMID: 23716265
  2. Enantioselective acute toxicity effects and bioaccumulation of furalaxyl in the earthworm (Eisenia foetida).  |  Qin, F., et al. 2014. Chirality. 26: 307-12. PMID: 24771637
  3. Environmental behavior of benalaxyl and furalaxyl enantiomers in agricultural soils.  |  Qin, F., et al. 2014. J Environ Sci Health B. 49: 738-46. PMID: 25065825
  4. Multiresidue pesticide analysis in nutraceuticals from green tea extracts by comprehensive two-dimensional gas chromatography with time-of-flight mass spectrometry.  |  Jia, W., et al. 2015. J Chromatogr A. 1395: 160-6. PMID: 25865796
  5. Acylamino acid chiral fungicides on toxiciepigenetics in lambda DNA methylation.  |  Yin, J., et al. 2017. Food Chem Toxicol. 109: 735-745. PMID: 28456568
  6. Enantiomerization and stereoselectivity in bioaccumulation of furalaxyl in Tenebrio molitor larvae.  |  Yin, J., et al. 2017. Ecotoxicol Environ Saf. 145: 244-249. PMID: 28743065
  7. Enantioselective toxic effects and digestion of furalaxyl enantiomers in Scenedesmus obliquus.  |  Cheng, C., et al. 2018. Chirality. 30: 1269-1276. PMID: 30238504
  8. From a Food Safety Prospective: The Role of Earthworms as Food and Feed in Assuring Food Security and in Valuing Food Waste.  |  Tedesco, DEA., et al. 2020. Insects. 11: PMID: 32403222
  9. Rapid and Sensitive Immunochromatographic Method-Based Monoclonal Antibody for the Quantitative Detection of Metalaxyl in Tobacco.  |  Ni, P., et al. 2020. ACS Omega. 5: 18168-18175. PMID: 32743191
  10. An Alternative Strategy for Screening and Confirmation of 330 Pesticides in Ground- and Surface Water Using Liquid Chromatography Tandem Mass Spectrometry.  |  Tóth, E., et al. 2022. Molecules. 27: PMID: 35335236
  11. Pesticide exposure and child growth in low- and middle-income countries: A systematic review.  |  Bliznashka, L., et al. 2022. Environ Res. 215: 114230. PMID: 36087771
  12. A New Biocontrol Tool to Fight Potato Late Blight Based on Willaertia magna C2c Maky Lysate.  |  Troussieux, S., et al. 2022. Plants (Basel). 11: PMID: 36297781
  13. Synthesis, Fungicidal Activity and Plant Protective Properties of 1,2,3-Thiadiazole and Isothiazole-Based N-acyl-N-arylalaninates.  |  Kalinina, TA., et al. 2023. Molecules. 28: PMID: 36615609

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Furalaxyl, 250 mg

sc-235222
250 mg
$55.00