Thiacloprid
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| Names | |
|---|---|
| IUPAC name
{(2Z)-3-[(6-Chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene}cyanamide | |
| Other names
[3-[(6-Chloro-3-pyridinyl)methyl]-2-thiazolidinylidene]cyanamide | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.129.728 |
| KEGG | |
PubChem CID |
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| UNII | |
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| Properties[1] | |
| C10H9ClN4S | |
| Molar mass | 252.72 g·mol−1 |
| Appearance | Yellowish crystalline solid |
| Density | 1.46 g·cm−3 at 20 °C |
| Melting point | 136 °C (277 °F; 409 K) |
| 185 mg/L at 20°C[2] | |
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 | |
Thiacloprid is an insecticide of the neonicotinoid class. Its mechanism of action is similar to other neonicotinoids and involves disruption of the insect's nervous system by stimulating nicotinic acetylcholine receptors. Thiacloprid was developed by Bayer CropScience for use on agricultural crops to control of a variety of sucking and chewing insects, primarily aphids and whiteflies.[1][3]
References
- 1 2 Thiacloprid Pesticide Fact Sheet, United States Environmental Protection Agency
- ↑ "Thiacloprid". Bayer CropScience Crop Compendium. Bayer CropScience. Retrieved 30 November 2011.
- ↑ Schuld M, Schmuck R (2000). "Effects of Thiacloprid, a New Chloronicotinyl Insecticide, On the Egg Parasitoid Trichogramma cacaoeciae". Ecotoxicology. 9 (3): 197–205. doi:10.1023/A:1008994705074. ISSN 0963-9292.
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