High-Performance Liquid Chromatographic Separation of 2-Hydroxy Fatty Acid Enantiomers on a Chiral Slurry- Packed Capillary Column

Abstract
Complete enantiomer separations of racemic 2-hydroxy fatty acids of C5-C18 as their 3,5-dinitrophenylurethane and methyl ester derivatives were achieved by high-performance liquid chromatography with a slurry-packed fused-silica capillary column (40 cm × 0.32 mm i.d.) with a chiral phase, N-(S)-2-(4-chlorophenyl)isovaleroyl-d-phenylglycine ionically bonded to 5-μm silica gel. The analysis was optimized by using a ternary mobile phase, n-hexane-1,2-dichloroethaneethanol, and UV detection at 226 nm.

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