someone explain HPLC to me like I have not read a paper in years
Trying to get a straight answer on this: someone explain HPLC to me like I have not read a paper in years. The system suitability argument, since it comes up whenever somebody posts a number without one. Before the sample result means anything, the instrument has to be shown to be fit that day: replicate injections…
Resolution between two peaks depends on retention, selectivity and efficiency. A shallower gradient buys retention and usually resolution, at the cost of peak width and run time.
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you cannot report to two decimals off that baseline
Did you run a blank between injections?
Small fix — 214nm, not 210. It matters for the comparison you are making with the other run.
That is area percent, not mass percent. The trace cannot give you the second one.