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Chemical compound From Wikipedia, the free encyclopedia
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]
Names | |
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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 | |
CompTox Dashboard (EPA) |
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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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Thiacloprid has been banned in France since September 1, 2018.[4] The 5 neonicotinoids banned in France are Acetamiprid, Clothianidin, Imidacloprid, Thiacloprid and Thiamethoxam.[5]
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