Start by asking what you are optimising for, because cost per milligram, documentation depth and lead time do not have a common winner.
Submitting to different laboratories introduces a method difference that commonly exceeds the supplier difference. Gradient slope alone can move a reported purity figure by a per cent in either direction.
Compare documentation on a fixed checklist rather than by impression: lot specificity, method section, chromatogram availability, quantified content, water and counter-ion figures, and whether the code is on the vial.
Gradient slope, column chemistry and detection wavelength all affect the reported purity figure, which is why the method section is the part that makes results comparable.
Nothing here is medical advice, and research-use compounds are not approved for human use.
Name the laboratory and the dates or the comparison cannot be reproduced.
edited 21 Apr 2026 by tobias_maartens — added a caveat about sampling