Public COA audit
BPC-157
Audited July 28, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 88
- Confidence
- 92%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- 3-2-45804
- Sample date
- 2025-08-04
- Issue date
- 2025-08-04
7-panel checklist
Had data + good, had data + bad, reported without pass/fail, or missing. Missing lowers thoroughness — you decide whether that panel matters; PeptIQ’s score still factors coverage.
1 of 7 present · 1 passed · 0 failed · 0 reported · 6 missing
Missing is a thoroughness gap — not automatically bad. PeptIQ’s legitimacy score still weighs panel coverage; you can down-weight panels that don’t matter for your use case.
Identity
Not on this COA · core
Compound identity confirmed (e.g. HPLC, mass spec).
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Purity
Not on this COA · core
Reported purity percentage for the analyte.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Heavy metals
Not on this COA
Lead, arsenic, cadmium, mercury, or similar limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Microbial
Not on this COA
Bioburden / microbial limits testing.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Endotoxin
Tested · passed · core
LAL or chromogenic endotoxin assay.
< 0.01 EU/mL
Sterility
Not on this COA
Sterility testing where applicable.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Residual solvent / water
Not on this COA
Residual solvents or water content limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
How to read this
Had data · good
Panel present with a pass (or clear acceptance).
Had data · bad
Panel present with a fail — a concrete quality signal.
Had data · unclear
Value reported without an explicit pass/fail mark.
Missing
Not on this certificate. Lowers thoroughness; you decide if that panel matters for your use case. PeptIQ’s score still factors coverage.
Findings
Evidence-linked observations from this audit.
Endotoxin testing performed
Chromogenic LAL assay shows < 0.01 EU/mL, passing the 0.1 EU/mL threshold. Positive and negative controls both passed as expected.
Lot number present
LOT #: 3-2-45804 clearly stated
Test date documented
Test performed 08/04/2025, analyst signature dated same day
Testing lab identified
BioRegen with contact information and verification instructions provided. QR code and validation key (BIOLABS2010) included for authenticity verification.
Limited scope - endotoxin only
This is a single-panel report focusing exclusively on endotoxin testing. No identity, purity, heavy metals, microbial, sterility, or solvent testing included. This is common for specialized endotoxin testing but means comprehensive quality cannot be assessed from this document alone.
Professional presentation
Document follows standard analytical report format with clear sections, reagent information, methodology details, and interpretation. Uses Thermo Fisher kit A39553 with documented standards and detection range.
PeptIQ COA reports analyze document content and publicly verifiable lab signals. They are educational and not a guarantee of product quality, legality, or safety. Always consult a qualified professional before making health decisions. We never publish purchase prices, shipping details, or uploader identity.