Chlorantraniliprole
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 Chlorantraniliprole 3D molecular model generated using Avogadro software
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| 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
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| Identifiers | |
3D model (JSmol)
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| 11247880 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 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 is an insecticide of the diamide class used for insects found on fruit and vegetable crops as well as ornamental plants.[1]
Chlorantraniliprole opens muscular calcium channels, in particular the ryanodine receptor, rapidly causing paralysis and ultimately death of sensitive species (IRAC class 28). The differential selectivity chlorantraniliprole has towards insect ryanodine receptors explains its low mammalian toxicity receptor.[2] Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact.
References
[edit]- ^ EPA Pesticides Fact Sheet: Chlorantraniliprole
- ^ Nauen, Ralf; Steinbach, Denise (27 August 2016). "Resistance to Diamide Insecticides in Lepidopteran Pests". In Horowitz, A. Rami; Ishaaya, Isaac (eds.). Advances in Insect Control and Resistance Management. Cham: Springer (published 26 August 2016). pp. 219–240. doi:10.1007/978-3-319-31800-4_12. ISBN 978-3-319-31800-4.
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