Broflanilide
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| IUPAC name
3-[benzoyl(methyl)amino]-N-[2-bromo-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-(trifluoromethyl)phenyl]-2-fluorobenzamide
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| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
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PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C25H14BrF11N2O2 | |
| Molar mass | 663.285 g·mol−1 |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H410 | |
| P273, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Broflanilide is a complex, polycyclic, organohalogen insecticide which provides a novel mode of action (MoA).
Mode of action
[edit | edit source]Upon its discovery by Mitsui Chemicals, Insecticide Resistance Action Committee (IRAC) created the new MoA Group 30 for Broflanilide.[1][2][3][4] Broflanilide is a meta-diamide GABA-gated Cl− channel allosteric modulator.[1][2][3][4] This - along with isoxazolines providing the same MoA, so far only fluxametamide - constitute the new MoA Group 30 in the IRAC classification scheme.[3]
Advantages
[edit | edit source]- No cross-resistance with existing MoAs.
- Shows high effectiveness against wireworms.
- Not systemic.[1]
Environmental Hazards
[edit | edit source]The EPA has stated that Broflanilide is "Likely to be Carcinogenic to Humans".[5]
Broflanilide meets the EPA Working Definition of PFAS. Note that "EPA considers any level of PFAS to be potentially toxicologically significant".[6]
Products
[edit | edit source]Products were registered in the United States in January, 2021,[7] and in Canada.[1] It is being sold under the brand names Cimegra (BASF)[8] and Teraxxa (BASF, the seed treatment form).[9]
References
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- ^ a b IRAC Mode of Action Classification, Annex 6, 2018
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