Dithiocarbamate pesticide, liquid

DITHIOCARBAMATE PESTICIDES, FLAMMABLE LIQUID, n.O.S., flssh-DITHIOCARBAMATE PESTICIDES, FLAMMABLE LIQUID, n.O.S., flash-DITHIOCARBAMATE PESTICIDES, LIQUID, TOXIC, n.O.S. 

Dithiocarbamate pesticides, liquid, flammable, toxic n.o.s., flashpoint less than 23 °C. 2772... 

Miles and Moye [171] have shown that several classes of nitrogen containing pesticides responded to a high performance liquid chromatography post-column reaction detector that employed ultraviolet photolysis with optional reaction with o-phthalicdicarboxaldehyde-2-mercaptoethanol followed by fluorescence detection. It was applied to the determination of jV-methylcarbamates, carbamoyl oximes, carbamethoic acids, dithiocarbamates and phenyl ureas, phenyl amides and phenyl carbamates in groundwater. See also Table 4.3. 

From these early studies, dithiocarbamates and their transition metal complexes soon found a host of applications. For example, as a result of their insoluble nature they are widely used in inorganic analysis (3,4). They can also be used to separate different metal ions by high-performance liquid chromatography (HPLC) (5-10) and capillary gas chromatography (GC) (11, 12), and find use as rubber vulcanization accelerators (13), fungicides (14), and pesticides (15). Concomitant with the development of these applications came a burgeoning interest in their general transition metal chemistry and the characteristics and properties of the complexes formed. 

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