How every Orvanta batch is tested, traced, and verified before it ships.
Every Orvanta peptide is held to a minimum purity of ≥98% by HPLC. We hold this line on every batch — no exceptions, no margin-of-error excuses. If a batch doesn’t meet spec, it doesn’t ship.
We don’t test our own product and ask you to trust us. Every production lot is sent to an independent analytical laboratory before it leaves our facility. The lab has no incentive to pass our compounds — their job is to report what’s actually in the vial.
HPLC (High-Performance Liquid Chromatography) — confirms purity. Tells us what percentage of the contents is the target compound versus impurities, degradation products, or synthesis byproducts.
Mass Spectrometry — confirms identity. Verifies the molecular weight and structure of the compound. Eliminates ambiguity about what’s actually in the vial.
LAL Assay (Limulus Amebocyte Lysate) — tests for bacterial endotoxins. Batches with detectable endotoxins are destroyed, not shipped.
Every vial we ship carries a unique lot code printed on the label. That code links to the specific Certificate of Analysis for that production run — not a generic COA, not a reused supplier document, not a sibling batch. The certificate you see is for the vial in your hand.
Batches that don’t pass any of the three tests are destroyed. They don’t get sold under a different label, blended into other lots, or downgraded to a budget tier. They’re gone.
Most suppliers hide their test results behind email requests, batch numbers you have to ask for, or PDFs sent only after purchase. We publish every COA the day the lab returns it. Browse the full library at COA Library — no request, no signup, no friction.
Email support@orvantalabs.com with any lot code or batch reference and we’ll send the underlying test report. We respond personally to every message.