by
lmh » Thu Mar 31, 2016 8:46 am
If you get the chance to run some normal-phase, reverse-phase and hilic methods, it gets easier to envisage why people like reverse phase so much.
Proper old-fashioned normal-phase with silica columns goes wrong at the merest sniff of water, so not only must you use nastier solvents anyway, but you also have to keep them specially dry. No one (except Andy Alpert; watch his posts, and read his papers!) really understands how hilic works, and it certainly seems very sensitive to changes in pH of the buffer, changes in sample solvent composition and many other factors too. Reverse phase, on the other hand, is embarrassingly robust; very often even quite inexpert method development gives enough separation to do the job. The solvents are simple to make up; buffering is rarely critical (you can very often get away with a simple water/acid mix). There is a huge range of almost indestructible columns available.
Having said all the above, you are right; hilic is a good method, and we should ideally choose the method that suits the analyte. If you have very polar compounds, it would be better to use Hilic than reverse phase. Of course polar compounds may also be suitable for various ion-exchange approaches, but these aren't always compatible with mass spec, whereas hilic is.