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Ion Pairing reagent/Phloxine B
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
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I'm testing for Phloxine B using 55% ACN with 0.03M TBAB at 548 nm. I'm getting peak splitting, could this be caused by too much ion pairing reagent, and what are the effects of using too much?
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How much you are injecting and what is the retention time? You might be seeing effect of large volume injection. Also, mixed-mode columns will allow you to avoid the use of IP reagent (it is attached to the surface of silica)
Vlad Orlovsky
HELIX Chromatography
My opinions might be bias, but I have about 1000 examples to support them. Check our website for new science and applications
www.helixchrom.com
HELIX Chromatography
My opinions might be bias, but I have about 1000 examples to support them. Check our website for new science and applications
www.helixchrom.com
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- Posts: 2
- Joined: Wed Mar 20, 2019 5:59 pm
I'm injecting 20 microliters. I noticed that if I use 65% with 0.01M TBAB, the peaks look completely different, and I cannot tell if it's the ACN or the TBAB.How much you are injecting and what is the retention time? You might be seeing effect of large volume injection. Also, mixed-mode columns will allow you to avoid the use of IP reagent (it is attached to the surface of silica)
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