Abstract
The chlorpheniramine enantiomers were separated with capillary zone electrophoresis using β-cyclodextrin as the chiral selector. The effects of the concentration of β-cyclodextrin, the electrolyte pH and organic modifier (urea) on the difference in apparent electrophoretic mobilities of the enantiomers were investigated.
| Original language | English |
|---|---|
| Pages (from-to) | 52-58 |
| Number of pages | 7 |
| Journal | Journal of Beijing Institute of Technology (English Edition) |
| Volume | 6 |
| Issue number | 1 |
| Publication status | Published - Mar 1997 |