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. Author manuscript; available in PMC: 2007 Nov 21.
Published in final edited form as: J Pharm Biomed Anal. 2007 Aug 2;45(2):295–303. doi: 10.1016/j.jpba.2007.07.026

Table 1.

Chromatographic results obtained on the Chirabiotic T column for the enantioselective separation of (R,S)-IF, (R,S)-2-DCl-IF and (R,S)-3-DCl-IF; where: k2 = the retention of the second eluting enantiomer, α = the enantioselectivity, Rs = enantiomeric resolution, MeOH = methanol, IPA = 2-propanol, EtOH = ethanol, ACN = acetonitrile. See text for chromatographic conditions.

Mobile Phase Ifosfamide 2-DCl-IF 3-DCl-IF

k2 α Rs k2 α Rs k2 α Rs
MeOH 2.2 1.3 1.5 4.0 1.3 2.2 5.2 1.2 1.8
IPA 10.3 1.9 1.9 26 1.6 4.4 40 1.4 2.4
ACN 4.1 1.0 - 1.5 1.0 - 1.5 1.0 -
ACN:IPA
(30:70)
1.7 1.1 0.73 2.8 1.0 0.70 3.5 1.1 0.90
MeOH:IPA
(35:65)
2.3 1.2 1.6 3.7 1.2 2.6 5.1 1.2 1.9
MeOH:IPA
(40:60)
2.0 1.2 1.8 3.6 1.2 2.6 4.6 1.2 1.9
EtOH:IPA
(50:50)
3.9 1.5 1.9 8.0 1.4 1.8 11.1 1.3 1.7
EtOH:IPA
(40:60)
4.2 1.5 2.2 6.1 1.4 1.8 12.9 1.3 2.0
EtOH:IPA
(70:30)
2.9 1.3 1.9 5.7 1.3 1.9 7.7 1.2 1.8