High performance liquid chromatographic separation of monoacylglycerol enantiomers on a chiral stationary phase |
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Authors: | Yutaka Itabashi Toru Takagi |
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Affiliation: | (1) Department of Chemistry, Faculty of Fisheries, Hokkaido University, Hakodate, Japan |
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Abstract: | High performance liquid chromatographic separation of monoacylglycerol enantiomers as di-3,5-dinitrophenylurethane derivatives was carried out on a chiral stationary phase, N-(S)-2-(4-chlorophenyl)isovaleroyl-D-phenylglycine chemically bonded tov-aminopropyl silanized silica. Complete separation of the urethane derivatives of racemic monoacylglycerols with saturated acyl groups of C12−C18 was achieved using a stainless steel column (25 cm long) packed with the 5μ particles, an isocratic elution at ambient temperature with a mixture of hexane/ethylene dichloride/ethanol as a mobile phase, and a UV detector. Thesn-1 enantiomers were eluted ahead of the correspondingsn-3 enantiomers. Complete separation of thesn-2 isomers from the corresponding enantiomers and partial separation of the enantiomer homologues differing by two acyl carbons also were observed. |
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