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Thiacloprid

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Title: Thiacloprid  
Author: World Heritage Encyclopedia
Language: English
Subject: Neonicotinoid, Insecticides, Attractive toxic sugar baits, Benzoylurea, Empenthrin
Collection: Chloropyridines, Insecticides, Nitriles, Organochlorides, Pyridines, Thiazolidines
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Thiacloprid

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
 N
ChEBI  YesY
ChEMBL  YesY
ChemSpider  YesY
DrugBank  YesY
Jmol-3D images Image
KEGG  YesY
PubChem
UNII  YesY
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).
 N  (: YesY/N?)

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. ^ a b Thiacloprid Pesticide Fact Sheet, United States Environmental Protection Agency
  2. ^
  3. ^
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