Chlorantraniliprole
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 Chlorantraniliprole 3D molecular model generated using Avogadro software
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| Names | |
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| 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
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| Identifiers | |
3D model (
JSmol ) |
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| ChEBI | |
| ChEMBL | |
ECHA InfoCard
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100.112.607 |
| EC Number |
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| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C18H14BrCl2N5O2 | |
| Molar mass | 483.15 g·mol−1 |
| Melting point | 209 °C (408 °F; 482 K) |
| Hazards | |
| GHS labelling: | |
 
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| 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 their standard state (at 25 °C [77 °F], 100 kPa).
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Chlorantraniliprole (Rynaxypyr) is an insecticide of the
Isoptera
(termite) species.
Chlorantraniliprole opens muscular
calcium channels, in particular the ryanodine receptor, rapidly causing paralysis and ultimately death of sensitive species. The differential selectivity chlorantraniliprole has towards insect ryanodine receptors explains the outstanding profile of low mammalian toxicity.[citation needed
] Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact.
Chlorantraniliprole is an active ingredient in the insecticidal products Ferterra (0.4% chlorantraniliprole), Scotts GrubEx1 (0.8% chlorantraniliprole), and Coragen (18.5% chlorantraniliprole).