In the total phenol test , when I added forinphenol reagent into NADES, my 96-well plate will produce yellow precipitate, resulting in the inability to detect absorbance.But I noticed the others did it successfully in the papers I have read. Did you meet such a situation during the experiment, and did you carry out other treatments before the total phenol test?
In terms of HPLC detection, I found that NADES may cause damage to the column. Are there some solutions unable to be separated by the column? So do I need to process them before analysis?
One of NADES is made of Choline Chloride and Glycerin with a molar ratio of 1:2, the other one is made of choline chloride and urea in a molar ratio of 1:2.
I'd be very grateful,if anyone can help me deal with my problems.