 | |
 Chlorantraniliprole 3D molecular model generated using Avogadro software | |
| Names | |
|---|---|
| Preferred IUPAC name 3-Bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide | |
| Other names Rynaxypyr, Coragen, Altacor | |
| Identifiers | |
3D model (JSmol) | |
| 11247880 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.112.607 |
| EC Number |
|
| KEGG | |
| UNII | |
| |
| |
| Properties | |
| C18H14BrCl2N5O2 | |
| Molar mass | 483.15 g·mol−1 |
| Melting point | 209 °C (408 °F; 482 K) |
| Hazards | |
| GHS labelling: | |
  | |
| Warning | |
| H319,H335,H410 | |
| P261,P264,P271,P273,P280,P304+P340,P305+P351+P338,P312,P337+P313,P391,P403+P233,P405,P501 | |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Chlorantraniliprole is an insecticide of thediamide class used for insects found on fruit and vegetable crops as well as ornamental plants.[1]
Chlorantraniliprole opens muscularcalcium channels, in particular theryanodine receptor, rapidly causing paralysis and ultimately death of sensitive species (IRAC class 28). The differential selectivity chlorantraniliprole has towards insectryanodine receptors explains its low mammalian toxicity receptor.[2] Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact.