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Phosphoric acid, dichloroSubject

Chlorothietane was subjected to reaction with dichloro derivatives of phosphorous acid to give, after heating the reaction mixture to 150°C, the acyclic compound thiophosphoric acid in low yields. ... [Pg.243]

Szathmary and Luhmann [50] described a sensitive and automated gas chromatographic method for the determination of miconazole in plasma samples. Plasma was mixed with internal standard l-[2,4-dichloro-2-(2,3,4-trichlorobenzyloxy) phenethyl]imidazole and 0.1 M sodium hydroxide and extracted with heptane-isoamyl alcohol (197 3) and the drug was back-extracted with 0.05 M sulfuric acid. The aqueous phase was adjusted to pH 10 and extracted with an identical organic phase, which was evaporated to dryness. The residue was dissolved in isopropanol and subjected to gas chromatography on a column (12 m x 0.2 mm) of OV-1 (0.1 pm) at 265 °C, with nitrogen phosphorous detection. Recovery of miconazole was 85% and the calibration graph was rectilinear for 0.25 250 ng/mL. [Pg.45]


See other pages where Phosphoric acid, dichloroSubject is mentioned: [Pg.239]    [Pg.218]   
See also in sourсe #XX -- [ Pg.1217 ]

See also in sourсe #XX -- [ Pg.1217 ]

See also in sourсe #XX -- [ Pg.1217 ]




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Phosphoric acid, dichloroSubject Friedel-Crafts reaction

Subject acidity

Subject phosphoric acid

Subject phosphorous

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