A CE separation of cytokinins and cytokinin ribosides and some other p
urine and pyrimidine bases has been developed. Two electrolyte systems
have been tested: 150 mM phosphoric acid, pH 1.8 and 50 mM sodium dod
ecylsulphate + 20 mM berate, pH 9.2. The migration times were measured
and the effects of the solute structures were discussed. Preliminary
experiments with plant extracts have been performed to identify the cy
tokinins and their ribosides. Both the systems can be used, but 150 mM
phosphoric acid is better suited for identification of cytokinins in
plant extracts, as the electropherograms are subject to fewer interfer
ences.