Difethialone
 | |
| Names | |
|---|---|
| IUPAC name
3-[3-[4-(4-Bromophenyl)phenyl]-1-tetralinyl]-2-hydroxy-4-thiochromenone | |
| Identifiers | |
104653-34-1  | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 10469311  |
| ECHA InfoCard | 100.118.383 |
| KEGG | C18695 |
| PubChem | 91771 |
| UNII | KOL4VXI5O0 |
| |
| |
| Properties | |
| C31H23BrO2S | |
| Molar mass | 539.49 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Difethialone is an anticoagulant used as a rodenticide.[1] It is considered a second generation agent.[2]
In May 2008, the United States Environmental Protection Agency banned the use of difethialone in consumer-use rodenticide products and also for exterior use by commercial applicators.[3][4]
References
- ↑ Nahas K, Lorgue G, Mazallon M (1989). "Difethialone (LM-2219): a new anticoagulant rodenticide for use against warfarin-resistant and -susceptible strains of Rattus norvegicus and Mus musculus". Ann. Rech. Vet. 20 (2): 159–64. PMID 2751229.
- ↑ Saravanan K, Kanakasabai R, Thiyagesan K (June 2003). "Field evaluation of difethialone, a new second generation anticoagulant rodenticide in the rice fields". Indian J. Exp. Biol. 41 (6): 655–8. PMID 15266918.
- ↑ EPA, OCSPP, OPP, US. "Restrictions on Rodenticide Products". www.epa.gov.
- ↑ "Regulations.gov". www.regulations.gov.
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