Public COA audit

Glutathione

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
72
Confidence
85%
Panels
4/7
Purity (printed)
99.86%

Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (4/7), 4 soft concerns, and notable note: "High purity confirmed". To improve: include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
GLUT-062026-1
Identity method
LC-MS
Sample date
2026-06-19
Issue date
2026-06-22

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.

4 of 7 present · 4 passed · 0 failed · 0 reported · 3 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).

    Glutathione

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.86%

  • Heavy metals

    Not on this certificate file

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

  • Microbial

    Tested · passed

    Bioburden / microbial limits testing.

    No Detectable Microbial DNA

  • Endotoxin

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    Pass (both replicates)

  • 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

    99.86% average purity (Vial 1: 99.82%, Vial 2: 99.90%) via HPLC-UV is within normal range for research-grade glutathione

  • Identity confirmed

    LC-MS confirms glutathione identity with mass confirmation spectrum provided

  • Endotoxin testing present

    LAL assay per USP <85> with two replicates, both pass at ≤0.05 EU/mL sensitivity

  • Microbial testing present

    PCR-based microbial analysis shows no detectable microbial DNA

  • Lot number present

    GLUT-062026-1 with accession number 2606190001 and search code Whol2606190001

  • Dates present and reasonable

    Received 2026-06-19, reported 2026-06-22 (3-day turnaround)

  • Lab verification unclear

    Freedom Diagnostics Testing website and email provided, but no independent accreditation (ISO 17025, etc.) or third-party verification mentioned on document

  • Generic presentation

    Document uses relatively simple formatting without detailed accreditation logos, regulatory compliance statements, or analyst signatures beyond 'Principal Chemist' title

  • Missing panels

    Heavy metals, sterility (USP <71>), and residual solvents/water content not tested or reported

  • Net content variance

    Vial 1 (1490.75 mg) is ~0.6% below labeled 1500mg, Vial 2 (1519.70 mg) is ~1.3% above; both within typical manufacturing tolerance but worth noting

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.