© 2026 Peptide Depot. All rights reserved.
August 7, 2026

A Certificate of Analysis (CoA) is the difference between a labeled vial and a characterized compound. It's the document that tells you what a peptide actually is, how pure it is, and how it was tested. For research use, that matters. Impurities, water content, and misidentified sequences all corrupt experimental data before you run a single assay.
Most buyers skim the purity number and move on. That's a mistake. A CoA carries several data points, and each one answers a specific question about the material. This guide walks through what a complete CoA should contain, how to read the analytical methods behind it, and the red flags that should make you pause.
Everything below refers to peptides sold for research use only — not for human consumption.
A CoA is a batch-specific analytical report. It records the identity, purity, and physical properties of one production lot. A generic CoA that isn't tied to a lot number is close to useless — it tells you about the product in theory, not the vial in your hand.
A complete CoA should include:
If the sequence isn't printed, you can't confirm the vendor is even selling what you ordered. That's the first thing to check.
Purity is usually reported as a percentage from HPLC peak area — commonly 95%, 98%, or 99%. The number reflects the proportion of the main peak relative to detected impurities. Higher is better, but the method behind it matters as much as the figure.
A few points worth understanding:
Deletion sequences — where an amino acid is missing during synthesis — are the most common impurity in solid-phase peptide synthesis. They can co-elute or show up as close side peaks on the chromatogram. A CoA that shows the actual trace lets you judge how clean the separation is.
The strength of a CoA is in the analytical methods, not the summary numbers. Two methods are non-negotiable for peptides.
HPLC separates the peptide from its impurities and quantifies purity by peak area. A reversed-phase HPLC trace should show a dominant main peak with minimal shoulders or satellite peaks. Look for the gradient conditions and column details when they're provided — they tell you the separation was set up properly.
Mass spec (often ESI-MS or MALDI-TOF) confirms identity by measuring the peptide's molecular weight. The observed mass should match the theoretical mass for the sequence within a small tolerance. This is how you confirm the vial contains the compound you ordered and not a similar sequence.
Lyophilized peptides absorb water. Karl Fischer titration measures residual moisture, which affects the net peptide content per vial. High water content means less actual peptide than the label weight suggests — relevant when you're standardizing concentrations across experiments.
For peptides used in cell culture or animal research, endotoxin testing (LAL assay) matters because bacterial endotoxins skew results in biological systems. Not every research application needs it, but if yours does, confirm it's on the CoA or ask for it.
Here's a practical order to work through a CoA when it lands in your inbox.
Once you've confirmed the material, researchers often use a Peptide Calculator to standardize concentrations across experiments so results stay comparable between lots.
Some patterns should slow you down:
A reputable Canadian supplier should provide batch-specific CoAs without friction. Peptide Depot publishes analytical documentation for its research compounds, and you can review the full product catalog to see what's available. When a compound like BPC-157 or semaglutide is described only by class — for example, a GLP-1 receptor agonist studied in metabolic research — the CoA is where you confirm the specific material behind that description.
Every synthesis run is slightly different. Purity, water content, and impurity profiles vary batch to batch, even from the same manufacturer using the same protocol. A CoA tied to one lot captures those differences; a generic spec sheet averages them away.
For reproducible research, this is the whole point. If you're comparing results across time, you want to know whether the material changed between runs. Batch-specific CoAs let you trace variability in your data back to the material — or rule it out. Keep the CoA for each lot on file alongside your experimental records.
A Certificate of Analysis (CoA) is a batch-specific document that reports a peptide's identity, purity, and physical properties. It typically includes the sequence, molecular weight, purity percentage, and the analytical methods used, such as HPLC and mass spectrometry.
Research-grade peptides are commonly offered at 95%, 98%, or 99% purity, measured by HPLC peak area. Higher purity reduces impurities like deletion sequences that can interfere with sensitive assays. Always look for a chromatogram supporting the stated purity, not just the number.
HPLC and mass spectrometry are the minimum. HPLC quantifies purity, and mass spectrometry confirms identity by matching observed to theoretical molecular weight. Karl Fischer titration for water content and endotoxin testing may also appear, depending on the intended research application.
The lot number ties the analytical data to a specific production run. Purity and impurity profiles vary between batches, so a CoA is only meaningful if its lot number matches the vial you received. A generic CoA with no lot number doesn't describe your actual material.
No. Peptides sold by Peptide Depot are for laboratory research use only and are not for human consumption. A CoA documents research-grade quality and identity; it is not a certification for any human or medical use.
A CoA is a research tool. Read it before you buy, keep it on file, and use it to confirm that the material in the vial matches your experimental assumptions. For more on sourcing and documentation, see the FAQ.
All products referenced are for research use only and not for human consumption.