Flupropadine
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Preferred IUPAC name 1-{3-[3,5-Bis(trifluoromethyl)phenyl]prop-2-yn-1-yl}-4-tert-butylpiperidine | |
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Properties | |
Chemical formula | C20H23F6N |
Molar mass | 391.401 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Flupropadine is a rodenticide.[1][2] Originally made by May and Baker[3] and tested on farms in the United Kingdom it was withdrawn from use by 1994.[4] Flupropadine has a delayed action, and so rodents can have multiple feeds from the bait before being killed.[5]
The molecule has two rings, one is a m-hexafluoroxylene, and the other is piperidine. Flupropadine is made from 3,5-bis(trifluoromethyl)iodobenzene, propargyl alcohol, and 4-tert-butylpiperidine.[6]
References
- ^ Buckle, A. P (1985). "Field trials of a new sub-acute rodenticide flupropadine, against wild Norway rats (Rattus norvegicus)". The Journal of Hygiene. 95 (2): 505–12. doi:10.1017/s0022172400062926. PMC 2129537. PMID 3840823.
- ^ Rowe, F. P; Bradfield, A; Swinney, T (1985). "Pen and field trials of flupropadine against the house mouse (Mus musculus L.)". The Journal of Hygiene. 95 (2): 513–8. doi:10.1017/s0022172400062938. PMC 2129553. PMID 4067302.
- ^ Missio, Andrea (14 June 2006). "Hexafluoroxylenes: Fluorine Chemistry and Beyond" (PDF). p. 7.
- ^ Berny, Philipe (May 2003). "STATE-OF-THE-ART REPORT ON THE USE OF ANTICOAGULANT RODENTICIDES IN THE EU AND BEYOND". Communication and Information Resource Centre for Administrations, Businesses and Citizens. Retrieved 15 May 2018.
- ^ Buckle, Alan P.; Smith, Robert H. (2015). Rodent Pests and Their Control, 2nd Edition. CABI. p. 116. ISBN 9781845938178.
- ^ Unger, Thomas A. (1996). Pesticide Synthesis Handbook. William Andrew. pp. 499–500. ISBN 9780815518532.
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Pest control: Rodenticides
Vitamin K antagonists
Coumarins / 4-Hydroxycoumarins |
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1,3-Indandiones |
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