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Isopestox

The basis of this analysis is said to be the formation of a peroxy phosphate compound (the Schoenemann reaction [49]). Oxidation of an amine such as 3,3 -dimethoxy benzidine or indole in a colorimetric reaction, or in the present case luminol with the emission of light then follows. Lucigenin does not work in this assay although it has been claimed as useful in the analysis of the nerve gas Tabun (5) [46]. Related insecticides such as Isopestox behave similarly [46-48]. Sensitivity can be improved by addition of chloride ion [52], enhancing the light yield, or by suppression of background chemiluminescence by complexation of trace transition metals by EDTA. [Pg.173]

See other pages where Isopestox is mentioned: [Pg.214]    [Pg.30]    [Pg.1117]    [Pg.1736]    [Pg.145]    [Pg.74]    [Pg.977]    [Pg.200]    [Pg.73]    [Pg.200]    [Pg.214]    [Pg.30]    [Pg.1117]    [Pg.1736]    [Pg.145]    [Pg.74]    [Pg.977]    [Pg.200]    [Pg.73]    [Pg.200]   
See also in sourсe #XX -- [ Pg.200 ]

See also in sourсe #XX -- [ Pg.200 ]

See also in sourсe #XX -- [ Pg.200 ]



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Demyelination by isopestox

Insecticides isopestox, octamethylpyrophosphoramide, parathion, paroxan

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