Onboarding · Document walkthrough

Reading your first COA.

When the parcel arrives, the COA is the document that tells you what you actually received. This walkthrough opens a sample certificate field by field, in plain language. No chemistry degree required.

How to read a COA covers the technical depth; this page is the onboarding companion — what every line says, why it is there, and what to do if it looks wrong.

Sample document

A sample COA, annotated.

The values below are illustrative only. Your batch will have its own numbers.

Sample Analytical Lab · Eindhoven, NL

Certificate of Analysis

Document # CoA-2026-04-1182

Compound name
BPC-157 (acetate)
CAS number
137525-51-0
Molecular formula
C62H98N16O22
Molecular weight
1419.53 g/mol
Batch / Lot
BPC0426-A
Manufacture date
2026-04-12
Retest date
2028-04-12
Appearance
White lyophilized powder
HPLC purity (area-%)
99.13 %
Mass spec (M+H)
1420.51 (matches expected)
Water content (Karl-Fischer)
4.2 %
Acetate content
8.6 %
Bacterial endotoxins
< 5 EU/mg
Released by
QC Analyst, signature on file

Field by field

What each line means.

Compound name · CAS number · Molecular formula · Molecular weight

This is identity. The name says what the molecule is called; the CAS number is the international registry ID for that exact molecule (no two compounds share a CAS); the molecular formula and molecular weight describe the structure. If any of these four lines does not match what is on the product page you ordered, stop — that is a packaging or paperwork mismatch and we want to know about it.

Batch / Lot · Manufacture date · Retest date

This is provenance. The batch number ties the COA to a specific synthesis run. The manufacture date is when the powder was made; the retest date is when the lab recommends re-analysing the material to confirm continued purity. Lyophilized peptides typically carry a two-year retest window when stored correctly. The batch number on this certificate must match the batch printed on the vial label.

Appearance

What the powder looks like. “White lyophilized powder” or “off-white lyophilized cake” are typical. If the vial you receive contains a cracked, melted or yellow-stained cake, document with a photo before reconstitution and contact support — that is usually a transit-temperature issue, not a content issue, but we still want the photo.

HPLC purity (area-%)

The headline purity number. 99.13 % means that of all the molecules detected by the chromatography, 99.13 % were the intended peptide. The remaining 0.87 % are typically synthesis side-products or fragments — not contamination from a different compound. Reputable COAs include the chromatogram (a graph of detector peaks); if the certificate is missing the picture, ask for it.

Mass spec (M+H)

Mass spectrometry confirms that the molecule has the mass it should. “M+H” is the molecule plus one hydrogen ion (the standard ionisation in positive-mode MS). 1420.51 matches the expected molecular weight (1419.53) plus a hydrogen, so the structure is confirmed. A purity test alone could be high while still measuring the wrong molecule; mass spec rules that out.

Water content (Karl-Fischer)

How much residual water is left in the lyophilized cake. Single-digit percentages are normal; very high values (> 10 %) indicate poor freeze-drying. Karl-Fischer is the analytical method — a titration that specifically reacts with water.

Acetate content

Most peptides ship as acetate salts (a chemistry artefact of the synthesis purification). The acetate contributes to the total weight in the vial — a 5 mg vial of “BPC-157 acetate” with 8.6 % acetate contains 5 mg of total powder, of which roughly 4.57 mg is the active peptide and 0.43 mg is acetate. Whether the labelled mass refers to peptide-base or salt-form is a question worth asking; this catalog labels by the salt form (total powder).

Bacterial endotoxins

Endotoxins are fragments of bacterial cell walls. The test is reported in EU/mg (Endotoxin Units per milligram). Low single-digit values are typical for research-grade material that has not been processed under sterile (pharmaceutical) conditions. This is a research test, not a sterility certification.

Released by · signature

A COA is a signed document. The signature line attributes the certificate to a specific QC analyst at the testing lab. Unsigned COAs are unfinished paperwork.

If something looks wrong

What to do if a field does not match.

  1. Identity mismatch (wrong name, CAS or molecular weight on the COA vs. what you ordered) → do not reconstitute. Photograph the vial and the COA, contact support with the order reference.
  2. Batch mismatch (vial batch differs from COA batch) → same as above. The COA must describe the vial in front of you.
  3. Visibly damaged cake (melted, cracked, discoloured) → photograph before reconstitution; contact support. Usually a transit-temperature issue.
  4. Missing chromatogram or signature → request the complete document from the supplier; an incomplete COA is not a finished one.
  5. Anything you do not recognise → the glossary defines every term used on the certificate; if it is still unclear after reading the definition, ask before you open the vial.

Next

Want the full technical document?

The How to read a COA page goes deeper into chromatography, mass spectrometry and assay specifics. The Peptide research 101 primer covers the surrounding context.

Technical COA guide Glossary