Complete Certificates of Analysis are published below for every product we offer — because at Oneday Compounds full transparency isn’t optional.
Every lot/batch released by Oneday Compounds undergoes independent third-party verification at a U.S. ISO-accredited labaoratory. We are leading the industry in what we believe should be the new testing standard. While others test “selectively”, we verify COMPREHENSIVELY with documentation. When data is fully transparent and published, trust is earned.
Oneday Compounds 7-Point Testing & Verification
Every lot is independently tested by an independent third-party ISO-accredited U.S. laboratory for Identity (HPLC fingerprinting), Net Content (Weight), Purity (>99% HPLC), Conformity, Sterility, Endotoxins, and Heavy Metals.
Trace metals can be present at extremely low background levels during chemical synthesis. Independent ICP-MS screening verifies that any detected trace levels that remain on our COAs are well within established international pharmaceutical safety thresholds relative to the quantity of material contained in each vial.
Sterility and Endotoxin levels are independently verified for every lot. Testing is performed using validated methods (USP <71>) for sterility and LAL for endotoxins) to confirm that all results remain within established acceptance thresholds for research materials prior to release.
Why This Matters
A Certificate of Analysis is more than a report — it is verifiable evidence that a specific batch has been independently 3rd-party tested and confirmed. Each COA documents identity, net content, purity, sterility, endotoxins, heavy metals, and conformity to specification, confirming the expected identity, purity, and consistency of each lot for rigorous scientific work. Researchers rely on these batch-specific analytical results to ensure consistency, eliminate uncertainty, and maintain confidence throughout their studies.
