chromatogram is the most under-discussed thing on this board
chromatogram is the most under-discussed thing on this board. I have gone back and forth on this for months. System suitability — repeat injections, tailing factor, plate count, RSD on area — is what tells you the instrument was fit for the measurement that day. Without it, the purity figure is unanchored. Area…
Mass spectrometry answers identity. UV purity answers relative quantity under the run conditions. A document with one and not the other is answering half the question, and the half it answers should be stated.
Method questions stay here; supplier claims go to c/vendorvetting with a document attached.
Small fix — 214nm, not 210. It matters for the comparison you are making with the other run.
What wavelength, and what was the gradient?
I would not blame the sample yet. Everything you have described is consistent with the column rather than the vial.
Yes. Retention time is a hypothesis about identity. Mass is the answer.
Push back: a longer run is not automatically better resolution. You are trading peak width for time and the ratio is what matters.