Third-party tested — Certificate of Analysis on every batch
V8 PEPTIDES
Guide5 min read

How to Read a Certificate of Analysis (COA)

A Certificate of Analysis (COA) is the analytical record for a specific production batch. It documents what testing was performed and what the results were, so a receiving lab can verify identity and purity before material enters a workflow.

The fields that matter

  • Compound identity & sequence — confirms the material matches what was ordered
  • Measured purity — the analytical purity value, with the method used (e.g. HPLC)
  • Molecular formula & mass — supports identity confirmation, often via mass spec
  • Batch / lot number — ties the document to the exact vial you received
  • Test date — when the analysis was run
  • Supplied form & storage — how the material was prepared and should be kept

Batch-specific beats generic

The single most important quality of a COA is that it's tied to your lot. A generic sheet that could apply to any batch tells you little. A batch-specific COA — with a lot number that matches your vial — is what supports genuine receiving and recordkeeping.

Red flags

  • No analytical method named next to the purity figure
  • No batch/lot number, or one that doesn't match the vial
  • A headline purity claim with no supporting document at all

Documentation on every product

≥98% purity, molecular identity, and a batch-specific COA.

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