{{Chembox | ImageFile = Fluopyram.svg | ImageSize = 200px | PIN = ''N''-{2-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]ethyl}-2-(trifluoromethyl)benzamide | OtherNames = | Section1 = {{Chembox Identifiers | CASNo = 658066-35-4 | CASNo_Ref = {{cascite|correct|CAS}} | UNII_Ref = {{fdacite|correct|FDA}} | UNII = F0VT7K5302 | PubChem = 11158353 | ChemSpiderID=9333461 | SMILES = FC(F)(F)c1ccccc1C(=O)NCCc2ncc(cc2Cl)C(F)(F)F | StdInChI=1S/C16H11ClF6N2O/c17-12-7-9(15(18,19)20)8-25-13(12)5-6-24-14(26)10-3-1-2-4-11(10)16(21,22)23/h1-4,7-8H,5-6H2,(H,24,26) | StdInChIKey=KVDJTXBXMWJJEF-UHFFFAOYSA-N }} | Section2 = {{Chembox Properties | C=16|H=11|Cl=1|F=6|N=2|O=1 | Appearance = | Density = | MeltingPtC = 117.5 | MeltingPt_ref = <ref name=fao>{{cite web | url = http://www.fao.org/fileadmin/templates/agphome/documents/Pests_Pesticides/JMPR/Evaluation10/Fluopyram.pdf | title = Fluopyram | publisher = Food and Agriculture Organization of the United Nations}}</ref> | BoilingPtC = 318–321 | BoilingPt_ref = <ref name=fao/> | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}
'''Fluopyram''' is a synthetic fungicide and nematicide used in agriculture.<ref>{{cite journal |last1=Grabau |first1=Zane J. |last2=Liu |first2=Chang |last3=Schumacher |first3=Lesley A. |last4=Small |first4=Ian M. |last5=Wright |first5=David L. |title=In-furrow fluopyram nematicide efficacy for Rotylenchulus reniformis management in cotton production |journal=Crop Protection |date=February 2021 |volume=140 |article-number=105423 |doi=10.1016/j.cropro.2020.105423|bibcode=2021CrPro.14005423G |s2cid=226354918 }}</ref><ref>{{cite journal |last1=Faske |first1=TR |last2=Hurd |first2=K |title=Sensitivity of Meloidogyne incognita and Rotylenchulus reniformis to Fluopyram. |journal=Journal of Nematology |date=December 2015 |volume=47 |issue=4 |pages=316–21 |pmid=26941460|pmc=4755706 }}</ref> 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).<ref name=mda>{{cite web | url = http://www.mda.state.mn.us/chemicals/pesticides/regs/~/media/Files/chemicals/reviews/nair-fluopyram.ashx | title = Fluopyram | work = New Active Ingredient Review | publisher = Minnesota Department of Agriculture | date = April 2012 | access-date = 2015-09-16 | archive-url = https://web.archive.org/web/20170426233624/http://www.mda.state.mn.us/chemicals/pesticides/regs/~/media/Files/chemicals/reviews/nair-fluopyram.ashx | archive-date = 2017-04-26 }}</ref>
==Regulation== Developed and produced by Bayer, it was approved in 2012 by the U.S. Environmental Protection Agency<ref name=mda/> and in 2013 it was approved in the EU for use as an active ingredient in pesticides.<ref>{{cite web | url = http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2013:225:0013:0016:DE:PDF | title = Durchführungsverordnung (EU) Nr. 802/2013 Der Kommission | language = German | date = August 2013}}</ref>
Pesticide products containing fluopyram have been banned in Denmark because the chemical can degrade into trifluoroacetic acid, which can then contaminate groundwater and not decompose.<ref>{{cite web |title=Denmark bans more PFAS pesticides to protect groundwater |url=https://www.pan-europe.info/blog/denmark-bans-more-pfas-pesticides-protect-groundwater |publisher=Pesticide Action Network Europe |access-date=6 November 2025 |date=October 6, 2025}}</ref>
==References== {{reflist}}
Category:Fungicides
Category:Nematicides
Category:Trifluoromethyl compounds Category:Benzamides Category:Chloropyridines