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. 2015 Dec 10;54(4):531–535. doi: 10.1093/chromsci/bmv177

Table I.

Effect of Content of Alcohols on the Enantioseparation of Six Antihistamines

Compound Isopropanol (modifier)
Ethanol (modifier)
tR1 tR2 α RS % tR1 tR2 α RS %
Doxylamine 43.242 48.635 1.13 0.36 5 22.684 25.795 1.16 0.41 5
23.199 10 14.547 10
Carbinoxamine 27.077 10 14.768 10
Cetirizine 46.722 56.422 1.22 1.43 5 18.987 21.357 1.15 2.02 5
25.037 30.295 1.24 1.76 10 12.157 13.383 1.14 1.87 10
14.513 17.308 1.25 1.88 20 8.666 9.348 1.12 1.59 20
11.167 13.159 1.25 1.66 30 7.128 7.637 1.13 1.47 30
10.578 12.254 1.22 1.53 40 6.819 7.213 1.11 1.30 40
Hydroxyzine 38.088 40.725 1.08 0.51 5 22.191 5
21.465 22.507 1.06 0.41 10 12.592 10
13.274 20 8.220 20
Oxomemazine >100 10 38.864 10
Dioxopromethazine >100 10 41.684 42.809 1.03 0.37 10
52.189 20 19.736 20.144 1.03 0.32 20
31.660 30 13.057 13.237 1.02 0.26 30
22.849 40 10.183 40

tR1, tR2: retention times (min); α: separation factor; RS: resolution factor; “–” means that separation was not seen. Chromatographic conditions. The basic solvent of mobile phase was n-hexane, the temperature was at 25°C and the flow rate was 0.8 mL min−1.