Pyriproxyfen
| Names | |
|---|---|
| IUPAC names
4-phenoxyphenyl (RS)-2-(2-pyridyloxy)propyl ether
2-[1-(4-phenoxyphenoxy)propan-2-yloxy]pyridine |
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| Identifiers | |
| 95737-68-1 |
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| ChEBI | CHEBI:39260 |
| ChemSpider | 82851 |
| Jmol interactive 3D | Image |
| KEGG | C18605 |
| PubChem | 91753 |
| UNII | 3Q9VOR705O |
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| Properties | |
| C20H19NO3 | |
| Molar mass | 321.369 g/mol |
| Density | 1.2 g/cm3 |
| Melting point | 46 °C (115 °F; 319 K) |
| Pharmacology | |
| ATCvet code | QP53 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Pyriproxyfen is a pyridine-based pesticide which is found to be effective against a variety of arthropoda.[1] It was introduced to the US in 1996, to protect cotton crops against whitefly. It has also been found useful for protecting other crops. It is also used as a prevention for fleas on household pets.
Pyriproxyfen is a juvenile hormone analog, preventing larvae from developing into adulthood and thus rendering them unable to reproduce.
In the US, pyriproxyfen is often marketed under the trade name Nylar. In Europe, pyriproxyfen is known under the brand names Cyclio (Virbac) and Exil Flea Free TwinSpot (Emax).
See also[edit]
- Methoprene
- Methoprene in the Pesticide Properties DataBase (PPDB)
- Pyriproxyfen in the Pesticide Properties DataBase (PPDB)
References[edit]
- ^ Ishaaya, I; Horowitz, AR (1995). "Pyriproxyfen, a Novel Insect Growth Regulator for Controlling Whiteflies : Mechanisms and Resistance Management". Pestic. Sci. 43 (3): 227–232. doi:10.1002/ps.2780430308.
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