DIRECT ENANTIOMERIC SEPARATION OF THE 4 STEREOISOMERS OF NADOLOL USING NORMAL-PHASE AND REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH CHIRALPAK-AD
Jp. Mccarthy, DIRECT ENANTIOMERIC SEPARATION OF THE 4 STEREOISOMERS OF NADOLOL USING NORMAL-PHASE AND REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY WITH CHIRALPAK-AD, Journal of chromatography, 685(2), 1994, pp. 349-355
Two enantiomeric separations have been developed which resolve the fou
r stereoisomers of nadolol on Chiralpak AD using high-performance liqu
id chromatography. The normal-phase method uses hexane, ethanol and di
ethylamine to baseline resolve all four stereoisomers. The reversed-ph
ase method uses ethanol, water and diethylamine. Both methods were opt
imized by investigating different mobile phase modifiers, flow-rates a
nd column temperatures. Accuracy and reproducibility were determined f
or quantitating levels of racemate A and racemate B using the normal-p
hase method.