A. Hickel et al., DETERMINATION OF ENANTIOMERIC PURITY OF MANDELONITRILE WITH DERIVATIZED CYCLODEXTRINS IN WATER, SPECT ACT A, 53(3), 1997, pp. 451-455
A variety of derivatized cyclodextrins was used for the determination
of the optical purity of mandelonitrile by H-1-NMR (nuclear magnetic r
esonance) spectroscopy in aqueous solution. Mandelonitrile was formed
by the enzymatic reaction of benzaldehyde and HCN (or acetone cyanohyd
rine) with the hydroxynitrile lyase (Hnl) from Hevea Brasiliensis (rub
ber tree). It turned out the the best separation was achieved with ace
tyl-beta-cyclodextrin (K-d=12 dm(3) mol(-1)). A straightforward integr
ation was possible if there was more than 5% of one of the enantiomers
in the solution. Below this value, the results were not reproducible
enough for quantitative analysis.