What we test, what we document, and what we will not claim.
No lot is released for sale until it has passed identity and purity testing. Testing is performed by independent analytical laboratories, and results are recorded on a batch-specific Certificate of Analysis tied to the lot number printed on your vial.
Our purity specification is ≥99% by HPLC for peptide catalog items. Lots that do not meet specification are not released.

The lot code is printed on the vial label and on your packing slip.
We return the batch-specific COA in PDF, typically within one business day.
A Certificate of Analysis reports measured analytical properties of a specific manufactured lot: chromatographic purity, mass confirmation, appearance, and quantity. That is its entire scope.
A COA is not evidence of safety, biological activity, efficacy, sterility, endotoxin status, or fitness for any particular application. It is not a drug approval, a pharmacopoeial certification, or a clearance for use in humans or animals. Materials supplied by Frontier Labs are not manufactured under pharmaceutical GMP, are not sterile-filled for administration, and are not tested for endotoxin unless expressly stated on the COA.
Lyophilized materials are shipped at ambient temperature and are stable in transit. On receipt, store sealed vials at -20 °C, desiccated and protected from light. Stated shelf life is 36 months from the date of manufacture for unopened vials stored as directed.
If a delivered lot does not match its Certificate of Analysis, contact us within 7 days of delivery with the lot number and a description of the discrepancy. Verified non-conforming material will be replaced or refunded in full. See our Shipping & Returns policy.