Public COA audit

Retatrutide

Audited September 5, 2026

Consistent with a legitimate COA

Document structure and test panels align with what we expect from authentic lab reports.

Legitimacy
95
Confidence
95%
Panels
3/7
Purity (printed)
99.04%

Scored high because document structure and panels look consistent with authentic lab output and limited panel coverage (3/7). To improve: include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
Blue Cap
Identity method
HPLC-RTM (chromatographic retention time comparison with reference standard)
Sample date
2026-05-27
Issue date
2026-06-05

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.

3 of 7 present · 2 passed · 0 failed · 1 reported · 4 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).

    Confirmed

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.04%

  • 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

    Not on this certificate file

    Bioburden / microbial limits testing.

    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.”

  • Endotoxin

    Tested · result on file · core

    LAL or chromogenic endotoxin assay.

    0.055 EU/mL

  • 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

    99.04% peptide purity by HPLC meets ≥95.0% specification. This is normal for research-grade peptides.

  • Identity confirmed

    Retatrutide confirmed by HPLC retention time match with reference standard. Fentanyl screen negative.

  • Batch information present

    Lot Number: Blue Cap, COA #: COA-2026-KLHVNE, Accession #: ACC-2026-3383

  • Dates consistent

    Sample received 2026-05-27, analyzed and issued 2026-06-05. All dates are valid and sequential.

  • Lab credentials present

    ILS Laboratories, San Diego CA. ISO/IEC 17025 accredited. Verification URL and QR code provided. Lab director signature present.

  • Core panels complete

    Identity, purity, and endotoxin testing performed. Heavy metals, microbial, sterility, and residual solvent panels not included in this report scope.

  • Endotoxin testing included

    Endotoxin result 0.055 EU/mL by USP <85> kinetic turbidimetric method. Report notes this is below commonly referenced thresholds for RUO products.

  • Professional presentation

    Document includes HPLC chromatogram, detailed methodology notes, QR verification code, and clear pass/fail indicators. Formatting consistent with legitimate analytical lab reports.

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.