Public COA audit

Retatrutide

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
93%
Panels
3/7
Purity (printed)
99.9%

Scored high because the document is mostly consistent but carries soft concerns, limited panel coverage (3/7), and 2 soft concerns. To improve: include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
tr9hd4t
Identity method
HPLC-UV-MS
Sample date
2026-05-05
Issue date
2026-05-19

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).

    ID Confirmed

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    >99.9%

  • 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.

    2.3 EU

  • 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 chromatographic purity

    HPLC-UV/MS shows >99.9% purity with clean chromatogram showing single dominant peak at ~7 min retention time

  • Mass spectral confirmation

    Mass spectrum shows expected m/z peaks (1586.2, 1194.0) consistent with Retatrutide; ID confirmed by comparison to authentic standard

  • Batch/lot number present

    Lot tr9hd4t clearly marked with photos of labeled vial

  • Date sequence logical

    Sample received 2026-05-05, testing dates 2026-05-08 to 2026-05-15, report issued 2026-05-19 - all dates are sequential and reasonable

  • Established testing laboratory

    Krause Analytical LLC is a known contract testing lab in Austin, TX; report includes verification URL, lab director signature, and detailed methods

  • Endotoxin testing performed

    Endotoxin result of 2.3 EU reported using USP 86 LAL method on 2026-05-15

  • Heavy metals method described but no results

    Page 4 describes ICP-MS method for metals testing (USP 233) but no results are reported in the certificate

  • Limited microbiology testing

    Only endotoxin testing performed; no microbial contamination, sterility, or residual solvent/water content testing reported

  • Professional presentation

    Multi-page report with chromatogram, mass spectrum, detailed methods, watermarks, and proper lab 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.