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
3ujjag4
Identity method
HPLC-UV-MS
Sample date
2026-03-16

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.

    1.9 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.

  • Excellent chromatographic purity

    HPLC purity >99.9% with clean chromatogram showing single dominant peak at 6.59 min

  • Mass spectral confirmation

    Mass spectrum matches reference standard for Retatrutide (CAS 2381089-83-2)

  • Potency within specification

    9.56 mg recovered vs 10 mg label claim = 95.6% of label, within typical acceptance range

  • Endotoxin testing performed

    Endotoxin level 1.9 EU per vial measured by USP 86 LAL method on 3/26/2026

  • Established testing laboratory

    Krause Analytical LLC is a known peptide testing lab in Austin, TX with verification URL provided

  • Complete traceability

    Lab #202940, Project 145128, Batch/Lot 3ujjag4, Test Certificate ID 3ujjag4

  • Logical date sequence

    Sample received 3/16/2026, HPLC testing 3/22/2026, endotoxin testing 3/26/2026 - all dates are sequential and on or before today (2026-09-05)

  • Professional presentation

    Multi-page report with chromatogram, mass spectrum, methods summary, and director signature

  • Limited microbial testing scope

    Only endotoxin testing performed; no sterility or microbial contamination panel present

  • Heavy metals testing not performed

    Methods summary describes USP/NF 233 ICP-MS metals testing procedure but no results reported for this sample

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.