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.
Journal of biochemical and biophysical methods, 54(1-3), 287-299 (2003-01-25)
The enantioselective high-performance liquid chromatography (HPLC) of three racemic 3-hydroxybenzodiazepines, oxazepam (Oxa), lorazepam (Lor), and temazepam (Tem), is a difficult operation because of the spontaneous chiral inversion in polar solvent. To solve this problem, we have developed an HPLC method
CYCLOBOND is the name given to Astec technology for bonding cyclodextrins to a high purity silica gel through a stable ether linkage.
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