By PeptideProof · Updated 12 October 2026 · 6 min read
Three numbers on a peptide COA are often treated as one: identity, purity and quantity. They are measured in different ways, answer different questions and fail in different ways. Knowing the difference is the quickest way to read a report more accurately.
| Result | Question it answers | Usual method |
|---|---|---|
| Identity | Is it the right molecule? | Mass spectrometry (LC-MS) |
| Purity | Of what was detected, how much is the main peptide? | HPLC with UV detection (often around 220 nm) |
| Quantity | How much peptide is actually there? | Assay against a reference standard |
Mass spectrometry measures the mass of molecules. For a peptide, the result is compared with the mass expected from its sequence. Peptides pick up several charges, so reports often show a charge state, for example [M+4H]4+, together with the measured value. If the measured mass does not fit the expected one, the sample is not what the label says, whatever the purity is.
An HPLC run separates the components of the sample and a detector records them as peaks. Purity is typically the area of the main peak divided by the total area of all peaks. Two limits matter:
Quantity (content or assay) compares the sample against a reference standard of known amount. This is the number to set against the amount on the label. Freeze-dried peptides are not 100% peptide by weight — counter-ions and residual water make up part of the powder — so how the laboratory defines “content” matters, and the method should be named.
A worked example
A vial is labelled 10 mg. The report shows purity 99.1% and quantity 9.3 mg. Read it as: the detected material is almost entirely the main peptide, and the vial holds about 93% of the declared amount. That is a gap of roughly 7% — within the range many assays vary by. If the quantity read 6.4 mg or 13 mg, purity would not explain the gap, and the question to ask is why.
Assay results commonly vary by several percent between methods and laboratories, and fill amounts differ slightly. As a rule of thumb, a gap under about 10% is rarely a concern on its own, while a larger gap deserves a question. PeptideProof flags a difference of 10% or more between the quantity found and the quantity declared as an observation — for example in the example report — never as a conclusion about a product.
For the whole document, not just these three numbers, see how to read a peptide COA.
See it on a real document
PeptideProof reads a COA for you and shows what is only reported, what has no evidence and what looks inconsistent. See an example first, or check your own — new accounts include free analyses.
Educational information about reading laboratory documents. It is not medical, dosing or purchasing advice, and it doesn’t say that any product is safe, legal or suitable for any use. See the medical and research-use disclaimer.