General description
On CYCLOBOND I 2000 SP, the hydroxyl groups on the surface of the β-cyclodextrin have been reacted with (S)-propylene oxide. This has the effect of extending hydrogen-bonding capabilities to accommodate analytes with chiral centers that are relatively distant from an aromatic ring structure. The (S)- form shows enhanced selectivity and efficiency for some separations, methadone, for example.
Bonded phase: (S)-Hydroxypropyl modified β-cyclodextrin
Resources:
CYCLOBOND FAQs
CYCLOBOND Reference Bibliography
Chiral Product Literature
Other Notes
Discover LiChropur reagents ideal for HPLC or LC-MS analysis
Recommended alternative 20024AST ASTEC® CYCLOBOND 2000 Chiral HPLC Column
See technical report
Legal Information
Astec is a registered trademark of Merck KGaA, Darmstadt, Germany

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