Public COA audit

GLP-3

Audited September 5, 2026

Mostly consistent, with concerns

Several fields check out, but we found issues worth reviewing before you rely on this document.

Legitimacy
92
Confidence
88%
Panels
5/7
Purity (printed)
99.77%

Scored high because the document is mostly consistent but carries soft concerns, broad panel coverage (5/7), and 1 soft concern.

Document details

Fields extracted from the certificate — not order or payment data.

Batch / lot
CR-3XAG20-2607-Black
Identity method
HPLC-UV/VIS
Issue date
2026-08-06

Original certificate

Embedded copy of the stored COA PDF or image. Download it for your records — PeptIQ’s audit is separate from the lab document itself.

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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.

5 of 7 present · 5 passed · 0 failed · 0 reported · 2 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

    Tested · passed · core

    Compound identity confirmed (e.g. HPLC, mass spec).

    Pass - Matches Ref. Standard

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.77%

  • Heavy metals

    Tested · passed

    Lead, arsenic, cadmium, mercury, or similar limits.

    As, Cd, Pb, Hg all ND

  • Microbial

    Tested · passed

    Bioburden / microbial limits testing.

    Total Aerobic <10 CFU/mL, Yeast/Mold <10 CFU/mL

  • Endotoxin

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    <5.00 EU/mg

  • Sterility

    Not on this certificate file

    Sterility testing where applicable.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

  • Residual solvent / water

    Not on this certificate file

    Residual solvents or water content limits.

    No evidence on this file. Vendors sometimes publish separate purity and endotoxin reports for the same lot — check the brand page before treating this as “never tested.”

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 on this file

Not on this certificate file. Lowers file thoroughness; a sibling endotoxin/purity report for the same lot may still exist. PeptIQ’s score still factors coverage.

Findings

Evidence-linked observations from this audit.

  • High purity confirmed

    99.77% chromatographic purity by HPLC-UV/VIS with clear chromatogram showing single major peak

  • Identity verified

    HPLC-UV/VIS confirms match to reference standard

  • Batch information complete

    Lot CR-3XAG20-2607-Black, Laboratory ID V260730-20 003, 20 mg amount

  • Issue date valid

    Released 8/6/2026, within acceptable timeframe

  • A2LA accredited laboratory

    Vanguard Laboratory references A2LA Certificate #6377.01.01, includes ISO 17025:2017 accreditation seal

  • Comprehensive testing suite

    Identity, purity, quantity, endotoxin, heavy metals (ICP-MS), and microbial bioburden all tested and passed

  • Sterility and residual solvents not tested

    No USP <71> sterility or residual solvent/water content panels present; common for research-grade materials but worth noting

  • Professional presentation

    Two-page report with chromatogram, product photo, signatures, proper disclaimers, and consistent branding

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.