In this technical tip, we will address the common issue of peak tailing encountered when working with basic analytes and “type A” silicas and offer two strategies to overcome it.
Early reversed phase columns were based on “type A” silicas, these materials had substantial metal contamination, causing the silanol groups on the surface of the silica to have greater and more variable activity. Manufacturers endcapped the materials as far as possible after bonding with C18 reagents, in an attempt to reduce the number of sites where ion exchange could take place. However basic compounds would generally tail badly. Let’s explore how we can overcome this limitation.
These strategies will help diminish the tailing effect but may not completely remove it as demonstrated in the below example chromatograms (Figure A and B).
Mobile Phase | 20 mM potassium phosphate buffer pH= 2.5 : Methanol (70:30) |
Flow Rate | 1 mL/min |
Detection | UV-Vis @254 nm |
Figure A shows the moderate effect of using an acidic pH to mitigate tailing for benzylamine, while Figure B shows the resulting chromatography after adding triethylamine as a modifier.
We recommend the use of type B (ultra-pure) silica in the development of new separations. Luna™ Omega fully porous and Kinetex™ Core-Shell columns provide excellent peak shape for challenging compounds.
Assessing the Impact of SecurityLINK™ PEEKsil Fingertight Fitting System on Increased Peak Efficiency and Reduction in Peak Asymmetry on Optimized Instrumentation.
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