| Active principle: CARBARIL |
| General schedule |
CHEMICAL NAME 1-naphthyl methylcarbamates (IUPAC) 1-naphthalenyl methylcarbamates (C.A.) UNPROCESSED FORMULA C H NO 12 11 2 CHEMICAL GROUP Carbamate nitrogen-organics HISTORICAL SIGNS Insecticide introduced in 1956 by Union Carbide Corp. (now Rhone-Poulenc Ag Co.). COMMON NAME carbaryl (BSI, ISO, ANSI, ESA) CAS NUMBER 63-25-2 CEE NUMBER 006-011-00-7 |
| Applicatory aspects |
EMPLOYMENT: Insecticide for the defense of fruit tree, vegetables (excluded mushrooms), potato, sugar beet, cereals, soy, sunflower, cotton, fodder, tobacco, floral, ornamental, forest, poplar, hatcheries, grassy carpets of golf and sport fields. RANGE OF ACTION: It has a polyvalent action. It is employed against the flea beetle, codling moth, Casside, cabbage butterfly, Cochineals, Leaf threatening, Meal moth, Moths, Tortrixs, Colorado beetle, Eulia, Cacecia, Cidia and Anarsia of the peach, Lepidoptera and Coleoptera in general. FORMULATIONS: Flowable - Granules - Wettable dust - Dry dust ABSORPTION AND TRANSLOCATION: It acts for direct contact and for ingestion from the bug to eliminate. It is endowed with cytotropich properties. COMPATIBILITY: It is miscible with the most common parasiticides at the exception of those that have an alkaline reaction. PHYTO-TOXICITY: It is not phyto-toxic, if it is applied in the normal conditions of employment. On some varieties of apple tree, if it is employed during the 30 days that follow to the flowering, it could provoke the thinning of the little fruits. USEFUL INFORMATIONS: In the application on some cultivars of apple tree, during the 30 days that follow the fall of the petals, it can provoke the thinning of the little fruits. Don't treat during the flowering. It is also gifted of molluscide action.
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