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| Names | |
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| Preferred IUPAC name
N-{2-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]ethyl}-2-(trifluoromethyl)benzamide | |
| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.127.749 |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C16H11ClF6N2O | |
| Molar mass | 396.72 g·mol−1 |
| Melting point | 117.5 °C (243.5 °F; 390.6 K)[1] |
| Boiling point | 318–321 °C (604–610 °F; 591–594 K)[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Fluopyram is a fungicide and nematicide used in agriculture.[2][3] It is used to control fungal diseases such as gray mold (Botrytis cinerea), powdery mildew, apple scab, Alternaria, Sclerotinia, and Monilinia. It is an inhibitor of succinate dehydrogenase (SDHI fungicide).[4]
Developed and produced by Bayer, it was approved in 2012 by the U.S. Environmental Protection Agency[4] and in 2013 it was approved in the EU for use as an active ingredient in pesticides.[5]
References
- ^ a b "Fluopyram" (PDF). Food and Agriculture Organization of the United Nations.
- ^ Grabau, Zane J.; Liu, Chang; Schumacher, Lesley A.; Small, Ian M.; Wright, David L. (February 2021). "In-furrow fluopyram nematicide efficacy for Rotylenchulus reniformis management in cotton production". Crop Protection. 140: 105423. doi:10.1016/j.cropro.2020.105423. S2CID 226354918.
- ^ Faske, TR; Hurd, K (December 2015). "Sensitivity of Meloidogyne incognita and Rotylenchulus reniformis to Fluopyram". Journal of Nematology. 47 (4): 316–21. PMC 4755706. PMID 26941460.
- ^ a b "Fluopyram". New Active Ingredient Review. Minnesota Department of Agriculture. April 2012. Archived from the original on 2017-04-26. Retrieved 2015-09-16.
- ^ "Durchführungsverordnung (EU) Nr. 802/2013 Der Kommission" (in German). August 2013.
This page was last edited on 28 August 2023, at 04:53