A Certificate of Analysis helps connect what is on the label to the documented batch record. Our product pages are built for clear review across every published testing category.
Product pages are built to support multiple document types per variant, so each testing category can be reviewed independently.
Purity & identity
Uses Mass Spectrometry to confirm the peptide is what the label says it is, with a clear look at identity and major impurities researchers should know about.
Cleaner identity and purity documentation helps reduce uncertainty when comparing batches or planning controlled work.
Net content
Uses High-Performance Liquid Chromatography (HPLC) to confirm the tested vial contains the labeled amount of peptide, giving researchers documented concentration details before the material reaches the lab.
You can plan research around documented concentration instead of relying on label claims alone.
Batch conformity
Compares additional vials from the same lot against the primary sample, adding confidence that the batch is consistent from vial to vial.
Batch-to-batch checks make it easier to compare results across repeat orders and longer research timelines.
Endotoxin safety
Uses Limulus Amebocyte Lysate (LAL) testing to track bacterial endotoxin documentation when available, supporting researchers working with sensitive cell culture or in vivo settings.
Contaminant screening gives researchers cleaner documentation before bringing a batch into sensitive workflows.
COA records are attached directly to the relevant product whenever documentation is available.
If a product has multiple strengths, use the variant selector in the testing section.
Check lot number, tested date, documented result, and the available COA link.
COA details are provided for research review only. They summarize available testing documentation at the time of analysis and do not represent medical advice, dosing guidance, or suitability for any human or animal use.
Quick answers for product documentation and batch records.
A Certificate of Analysis is a document from an independent laboratory that verifies the purity, identity, and quality profile of a peptide or research material. It can include results from methods such as HPLC analysis, Mass Spectrometry, net content review, and other quality control measures.
Product pages include Certificate of Analysis details when batch documentation is available for that product and variant. You can also request help finding a specific COA by emailing testing@aminologic.com with your order number, product name, and any lot details you have.
Key sections can include purity percentage, molecular weight or identity confirmation, appearance, net content, sequence or compound identification, tested date, and batch or lot number. Product pages organize these details so researchers can review the relevant documentation before ordering.
AMINOLOGIC is built around independent third-party documentation from qualified laboratories. When a specific batch record is published, the COA or supporting documentation should identify the lab and available testing details for that batch.
Testing is handled at the batch level. Published COA records are tied to the relevant product, variant, and lot so researchers can review the current available documentation for the material being supplied.
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