Pirimiphos-methyl
Names | |
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Preferred IUPAC name
O-[2-(Diethylamino)-6-methylpyrimidin-4-yl] O,O-diethyl phosphorothioate | |
Other names
Pirimifos-methyl
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Identifiers | |
CAS Number
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3D model (JSmol)
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755726 | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.045.011 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
UN number | 3082 2902 |
CompTox Dashboard (EPA)
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InChI
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Properties | |
Chemical formula
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C11H20N3O3PS |
Molar mass | 305.33 g·mol−1 |
Appearance | Straw-colored liquid |
Density | 1.147 g/mL (30 °C) |
Melting point | 15 to 18 °C (59 to 64 °F; 288 to 291 K) |
Boiling point | decomposes before boiling |
5.0 mg/L (30 °C) | |
Hazards | |
GHS labelling: | |
Pictograms
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Signal word
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Warning |
H302, H410 | |
Precautionary statements
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P264, P270, P273, P301+P312, P330, P391, P501 |
Flash point | 46 °C (115 °F; 319 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Pirimiphos-methyl, marketed as Actellic,[1][2][3][4] and Sybol is a phosphorothioate used as an insecticide. It was originally developed by Imperial Chemical Industries Ltd., now Syngenta, at their Jealott's Hill site and first marketed in 1977, ten years after its discovery.[5][6]
This is one of several compounds used for vector control of Triatoma. These insects are implicated in the transmission of Chagas disease in the Americas.[7] Pirimiphos-methyl can be applied as an interior surface paint additive, in order to achieve a residual pesticide effect.
Pyrimiphos-ethyl is a related insecticide in which the methoxy groups are replaced with ethoxy groups.
References[]
- ^ "Actellic50EC". www3.syngenta.com. Retrieved 2015-11-11.
- ^ "Common Chemistry - Substance Details - 29232-93-7 : Phosphorothioic acid, O-[2-(diethylamino)-6-methyl-4-pyrimidinyl]O,O-dimethyl ester". www.commonchemistry.org. Retrieved 2015-11-11.
- ^ "Actellic 50 EC". www3.syngenta.com. Retrieved 2015-11-11.
- ^ "ACTELLIC 50 EC: FIŞA CU DATE DE SECURITATE" (PDF) (in Romanian). Syngenta. 2013. Archived from the original (PDF) on 2016-09-10. Retrieved 2015-11-11.
- ^ "Syngenta: Celebrating 75 years of scientific excellence at Jealott's Hill International Research Centre" (PDF). Archived from the original (PDF) on October 11, 2007. Retrieved June 26, 2012.
- ^ Snell, B.K.; et al. (1978). "Chapter 11: Pyrimidine insecticides". In Peacock, F.C. (ed.). Jealott's Hill: Fifty years of Agricultural Research 1928-1978. Imperial Chemical Industries Ltd. pp. 98–109. ISBN 0901747017.
- ^ CHAPTER 3: Triatomine bugs, Vectors of Chagas disease, World Health Organization
External links[]
- Pirimiphos-methyl in the Pesticide Properties DataBase (PPDB)
Categories:
- Acetylcholinesterase inhibitors
- Phosphorothioates
- Pesticides
- Aminopyrimidines
- Diethylamino compounds
- Methoxy compounds
- Organic compound stubs