Education library

Lab literacy

Reading a Certificate of Analysis

Updated 2026-05-20

Gloved hands holding test tubes in a laboratory.
Research Use Only · All content on Peptidology is provided for research and educational purposes only. Materials discussed are Research Use Only (RUO) and are not for human or animal consumption. Nothing here is medical advice or instruction for human use.

A Certificate of Analysis (COA) is a lab's signed statement describing what a specific batch of material is and how pure it is. For research materials, the COA is the single most useful document a buyer can read — but only if you know what each section means and what it leaves out.

What a COA can and cannot tell you

A COA reports measurements made on one batch. It is not a guarantee about future batches, and it is not a safety endorsement. A strong COA tells you the identity of the material, its measured purity, and the analytical methods used to reach those numbers. A weak COA shows a number with no method, no batch ID, and no lab attribution.

The sections that matter

  • Identity confirmation. Mass spectrometry (MS) or another orthogonal method should confirm the molecule is what the label claims. A purity number is meaningless if identity was never established.
  • Purity by HPLC. High-performance liquid chromatography separates the target from impurities. Look for the actual chromatogram, not just a quoted percentage.
  • Batch / lot number. The COA should reference a specific lot that matches the physical product.
  • Lab attribution. An independent, accredited lab (for example, ISO/IEC 17025 scope) carries more weight than an unnamed "in-house" result.
  • Date and signatory. Recent, signed, and traceable to a person or lab.

Red flags

  • A purity percentage with no chromatogram and no method.
  • No batch number, or a batch number that does not match the product.
  • Identity "confirmed" by appearance or solubility rather than MS.
  • A COA that is reused across visibly different products.

A COA is evidence, not marketing. When a vendor publishes complete, per-batch documentation from an independent lab, you can evaluate their claims yourself — which is exactly what our vetting methodology rewards.

References

  1. USP <1226> Verification of Compendial Procedures
  2. ISO/IEC 17025 — testing and calibration laboratories