The 14-point Healix standard
Every batch is independently verified in an ISO/IEC 17025-aligned laboratory before it can ship. Here's exactly what that means.
Identity & purity
Mass spectrometry confirms the molecular identity of every batch, while reverse-phase HPLC quantifies purity against a ≥99% specification. Net peptide content and counter-ion analysis complete the compositional picture.
Safety screening
Each lot is screened for endotoxins and bioburden, with residual-solvent and heavy-metal panels run to pharmacopeia-aligned thresholds. Moisture is verified by Karl Fischer titration to protect long-term stability.
Traceability
Every vial carries a lot number tied to its full analytical record. Enter it on our Lab Results page — or scan the vial's QR code — and the exact Certificate of Analysis for that batch is in front of you in seconds.
Know exactly what's in every vial
Guesswork has no place in research. Every Healix batch passes a 14-point analytical panel in an ISO/IEC 17025-aligned laboratory before it ever reaches your bench — and the results ship with your order.
- Identity confirmation by mass spectrometry (MS)
- Purity quantified via reverse-phase HPLC
- Net peptide content & counter-ion analysis
- Endotoxin and bioburden screening
- Residual solvent and heavy-metal panels
- Appearance, solubility & moisture (Karl Fischer)
CERTIFICATE OF ANALYSIS
Lot 240515A · BPC-157
Scan the QR on any vial to pull its exact analytical report.
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