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N-Bromosuccinimide—Robinetin

Dipping solution I Dissolve SO mg N-bromosuccinimide in SO ml acetone [3]. Dippii solution II Dissolve SO mg robinetin in 70 ml ethanol [3]. [Pg.89]

It is assumed that the hydrogen bromide released on the oxidation of thiophosphoric acid insecticides with N-bromosuccinimide or bromine vapors forms intensely fluorescent salt-like derivatives with 3-hydroxyflavones — such as robinetin [1, 2, 4]. [Pg.89]

See other pages where N-Bromosuccinimide—Robinetin is mentioned: [Pg.89] [Pg.89] [Pg.90] [Pg.91] [Pg.331] [Pg.332] [Pg.824] [Pg.89] [Pg.90] [Pg.91] [Pg.345] [Pg.89] [Pg.89] [Pg.90] [Pg.91] [Pg.331] [Pg.332] [Pg.824] [Pg.89] [Pg.90] [Pg.91] [Pg.345]

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Bromosuccinimide

N-Bromosuccinimid

N-Bromosuccinimide

Robinetin