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Chlorodimeform

Amitrole (i. e., a weakly basic pesticide) and the insecticide Dimefox (tetra-methyl phosphorodiamidic fluoride) have been shown to be adsorbed by HA through ionic bonding [17, 151-153]. The interaction between the cationic pesticide Chlorodimeform and SPHA was studied and, based on IR data, Maqueda et al. [154] indicated that an ion exchange bonding mechanism occurred. [Pg.133]

The principal source of 4-chloro-ort/zo-toluidine in the enviromnent was as an impurity and as a decomposition (metabolic) product of chlorodimeform. This pesticide is no longer produced (WHO, 1998). [Pg.326]

Using 3rd instar larvae of the diamondback moth Plutella xylostella), the antifeedant and insecticidal activities of sixteen quassinoids were compared with those of known insect antifeedant chlorodimeform (= galecron), as shown in Table 16. The insecticidal activity of quassin (78) was higher than that of chlorodimeform, although its antifeedant activity was nearly identical to that of the reference compound [39]. [Pg.319]


See other pages where Chlorodimeform is mentioned: [Pg.184]    [Pg.319]    [Pg.184]    [Pg.319]   
See also in sourсe #XX -- [ Pg.319 ]




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Antifeedant activity of chlorodimeform

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