Dear all,
While developing an analytical method for GC, I have realised that one of the reagents contains traces of my analyte from the factory. It seems impossible to get this reagent impurity free.
Therefore my question is:
How valid would it be as a method if I subtract the blank peak area from any sample?
Does this impair the whole method and, therefore I should be thinking of finding another one?
Would it be ok if I draw a calibration curve crossing the ordinate axis above 0?
What would you do in my situation?
Regards