This is the question where methodology matters more than the conclusion.
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.
To compare properly: order the same compound at the same nominal strength from each supplier, submit all samples to the same laboratory in the same submission if possible, and ask for the same test set on each.
Inter-laboratory spread on identical peptide material is routinely half a per cent to a per cent by RP-HPLC, which is the noise floor for any cross-laboratory comparison.
Nothing here is medical advice, and research-use compounds are not approved for human use.
One laboratory, one method, one submission. Otherwise it is not a comparison.
edited 29 Jun 2026 by m_haraldsen — fixed an arithmetic slip in the third paragraph