Fludioxonil

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Fludioxonil
Fludioxonil.svg
Fludioxonil 3D BS.png
Names
Preferred IUPAC name
4-(2,2-Difluoro-2H-1,3-benzodioxol-4-yl)-1H-pyrrole-3-carbonitrile
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.125.684 OOjs UI icon edit-ltr-progressive.svg
KEGG
PubChem CID
UNII
  • InChI=1S/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H
    Key: MUJOIMFVNIBMKC-UHFFFAOYSA-N
  • InChI=1/C12H6F2N2O2/c13-12(14)17-10-3-1-2-8(11(10)18-12)9-6-16-5-7(9)4-15/h1-3,5-6,16H
    Key: MUJOIMFVNIBMKC-UHFFFAOYAI
  • c1cc(c2c(c1)OC(O2)(F)F)c3c[nH]cc3C#N
Properties
C12H6F2N2O2
Molar mass 248.189 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fludioxonil is a synthetic phenylpyrrole chemical introduced by Ciba-Geigy (now Syngenta) in 1993 for use as a non-systemic fungicide. It is a structural analog of the natural fungicide pyrrolnitrin.

Contents

It is used for the treatment of crops, particularly cereals, fruits and vegetables, and ornamental plants. It is often used in combination with another fungicide such as Cyprodinil. There was a particularly bad crop failure due to multiresistant B. cinerea in strawberry in Florida in 2012; in that year and many other years, fludioxonil was the only fungicide still providing any protection. [1]

Its mode of action is to inhibit transport-associated phosphorylation of glucose, which reduces mycelial growth rate. [2] Fludioxonil is used against Fusarium , Rhizoctonia , Alternaria , Botrytis cinerea , and Stromatinia cepivora .

Nectarines treated with fludioxonil Nectarines treated with fludioxonil.jpg
Nectarines treated with fludioxonil

Brand names include seed treatments: Celest, Agri Star Fludioxonil 41 ST, Dyna-shield Fludioxonil, Maxim 4 FS, and Spirato 480 FS, as well as foliar applications: Switch (fludioxonil + cyprodinil). [3]

Environmental and Health hazards

It is toxic to fish and other aquatic organisms. [4] It has been detected as a residue in baby foods. [5]

See also

References

  1. ↑
    • Hahn, Matthias (2014-05-28). "The rising threat of fungicide resistance in plant pathogenic fungi: Botrytis as a case study". Journal of Chemical Biology . 7 (4). Springer: 133–141. doi:10.1007/s12154-014-0113-1. ISSN   1864-6158. PMC   4182335 . PMID   25320647.
    • Mari, Marta; Di francesco, Alessandra; Bertolini, Paolo (2014). "Control of fruit postharvest diseases: old issues and innovative approaches". Stewart Postharvest Review . 10 (1). Stewart Postharvest Solutions: 1–4. doi:10.2212/spr.2014.1.1. ISSN   1745-9656. S2CID   85221316.
    • Amiri, A.; Heath, S. M.; Peres, N. A. (2013). "Phenotypic Characterization of Multifungicide Resistance in Botrytis cinerea Isolates from Strawberry Fields in Florida". Plant Disease . 97 (3). American Phytopathological Society: 393–401. doi:10.1094/pdis-08-12-0748-re. ISSN   0191-2917. PMID   30722364. S2CID   73422752.
  2. ↑ "Fludioxonil (Ref: CGA 173506)".
  3. ↑ "What's on your seed?" (PDF). Integrated Pest and Crop Management, University of Wisconsin-Madison.
  4. ↑ Paranjape, Kalyani, Vasant Gowariker, V. N. Krishnamurthy, and Sugha Gowariker. The Pesticide Encyclopedia. CABI, 2014.
  5. ↑ Evans, Sydney; Lacey, Anthony (November 15, 2023). "Pesticides still found in baby food, but biggest toxic threats eliminated". Environmental Working Group. Retrieved 25 November 2023.
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