A Certificate of Analysis, or COA, is a lab's report on a peptide batch. It is the one document that shows what the lab tested and what it found. Most people are handed one and have no idea what to look for. Here are the seven checks that matter, in plain language.
Does the report confirm the compound is what the label says? A good COA names the compound and shows a mass-spec or HPLC identity match that conforms.
What percentage of the sample is the actual peptide versus impurities? The bar for quality research material is 98% or better by HPLC.
How much peptide is actually in the vial versus the label claim? Net content should land close to 100% of the stated amount, not far under or over.
Bacterial endotoxin should test at or below the reported limit. A blank here means the test was not run, not that it passed.
A sterility result should read no growth. Again, a missing line means untested, not clean.
Lead, cadmium, arsenic, and mercury should each read negative or below limit.
On a multi-vial batch, the values should be consistent vial to vial rather than one good sample carrying the lot.
A full COA answers all seven. A partial report is not a failure, it just means fewer tests were run: an honest read is "incomplete, ask for a full panel", never "unsafe". A single missing line means untested, not passed. The grader at the top of this page reads a COA against these seven gates in seconds and explains each one. It needs no account, it keeps nothing, and it is the same grader the TR8CE app runs.
A Certificate of Analysis is a lab report on a specific batch. It states the identity, purity, and content of the material and may include safety tests, telling you whether the vial matches its label.
Quality research material reads 98% purity or better by HPLC, with net content close to 100% of the labeled amount.
New compounds on the shelf, new lab reads, and the numbers behind them. One email when it matters, from tim@tr8ce.app.
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