Thiacloprid

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]

Quick facts Names, Identifiers ...
Thiacloprid
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)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.129.728 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10- checkY
    Key: HOKKPVIRMVDYPB-UVTDQMKNSA-N checkY
  • Clc1ncc(cc1)CN2C(=N\C#N)\SCC2
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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Regulation

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]

References

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