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- W2013281904 abstract "In the capillary electrophoretic separation of primary amine enantiomers using (+)-(18-crown-6)-tetracarboxylic acid (18C6H4) as a chiral selector, the presence of run buffer constituents such as tris(hydroxymethyl)aminomethane (Tris) or Na+ competing with analytes for 18C6H4, diminishes the effectiveness of 18C6H4. In order to determine appropriate buffer systems for 18C6H4, various run buffer cationic components including Tris, 1,3-bis[tris(hydroxymethyl)methylamino]propane, bis(2-hydroxyethyl)iminotris(hydroxymethyl)methane, triethanolamine, tetramethylammonium, and Na+ were compared. Quantitative studies of the effects of the competitive constituents were carried out by measuring the electrophoretic mobilities of histidine as a function of the 18C6H4 concentration. We also derived a simple equation to estimate the optimal chiral selector concentration for a maximum mobility difference in the presence of a competitive inhibitor." @default.
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- W2013281904 date "2001-12-01" @default.
- W2013281904 modified "2023-10-06" @default.
- W2013281904 title "Comparative studies of various run buffers for chiral capillary electrophoresis using chiral crown ether as a chiral selector" @default.
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- W2013281904 doi "https://doi.org/10.1002/1522-2683(200112)22:20<4362::aid-elps4362>3.0.co;2-8" @default.
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