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  Česky / Czech version Čes. slov. Farm. 52, 2003, No. 3, p. 136–140
 
TLC and HPLC Separation of Positional Isomers of Alkylesters of 2-, 3-, 4- {2-Hydroxy-3- -[(4-diphenylmethyl)piperazine-1-yl]propoxy}phenylcarbamic Acid and Their Lipo-Hydrophilic Properties 
OPATŘILOVÁ R., BLEŠOVÁ M., CSÖLLEI J. 

Ústav chemických léčiv Farmaceutické fakulty Veterinární a farmaceutické univerzity, Brno
 


Summary:

       The paper deals with chromatographic separations of newly prepared substances, aryloxyaminopropanol derivatives. The derivatives represent three homological series of four carbons and four groups of positional isomers (methyl- to butyl- in positions 2-, 3, and 4-). Thin-layer adsorption chromatography employed the foil Silufol® UV 254 as the stationary phase and partition chromatography, commercially produced glass plates DC Fertigplatten MERCK RP-8 F254 S. High-performance liquid chromatography was used to separate positional isomers on the column SupelkosilTM ABZ+PLUS. The mobile phase was methanol and acetonitrile in graded rations with water and various flow rates of the mobile phase were tested. Partition chromatography, determination of partition coefficient in the system octanol-water, and the values of capacity factors k’ of the substances was employed to evaluate their lipophilicity.

        Key words: HPLC – TLC – positional isomers – aryloxyaminopropanol – lipophilicity
       

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