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- Posts: 8
- Joined: Mon Dec 10, 2007 8:56 am
The following conditions were used for the analysis: flowrate 1.0 mL/min; eluent 0.005 M HClO4 aqueous solution/CH3CN = 90/10; oven temperature 40oC; UV/vis detector 220 nm.
However, i find that the RsPak De-413L is not able to separate these compounds (phenol, catechol and guaiacol) and when analyzed in HPLC, it will come out together as 1 peak. Is there anyway to make this compounds eluted separately in HPLC. I would like advice on this matter.
