Reused chromatograms across lots: how to spot it — what changed since posts 31–40
This is a continuation of a long topic, addressed by post number rather than by page. Start at post 1 · go to the accepted answer.
Marking my uncertainty on Reused chromatograms across lots explicitly. I am confident about the direction, much less confident about the size, and not confident at all that it generalises past the case in the first post.
Narrowing post #30, because the general version has more than one answer.
If someone has run Reused chromatograms across lots properly I would rather read that than my own reconstruction of it. Posting mine only because the thread has gone quiet.
Post #33 is the version of this I will quote in future. One addition.
A chromatogram supplied as a small image is legible for peak shape and not for baseline detail. That is enough to sanity-check an integration and not enough to reproduce it.
Reading back through the Reused chromatograms across lots threads from last year, the same three questions come up every time and only one of them has ever been answered properly. That seems like a documentation gap rather than a knowledge gap.
Reused chromatograms across lots is well covered in the tag pages, and the older discussions are better than the recent ones because they were argued out properly. Worth twenty minutes before adding to this one.
Answering the question post #36 raises rather than the one it answers.
An itemised related-substances table with retention times says considerably more about the synthesis than a single total. A total tells you how much is not the main peak and nothing about what it is.
The mechanism is plausible, which is not the same as established.
I had written a reply contradicting post #36 and deleted it. Here is what survived.
Answering the Reused chromatograms across lots question as asked, then the question I think is meant. As asked: yes, with the qualification below. As meant: it depends on how the first measurement was taken.
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