Public COA audit

GLP-RT · Reta Peptide

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
85
Confidence
88%
Panels
3/7
Purity (printed)
99.98%

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
0010
Identity method
HPLC with UV Detection Coupled with Mass Spectrometry (LCMS/MS)
Sample date
2025-11-19
Issue date
2025-11-21

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 · 3 passed · 0 failed · 0 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).

    GLP-RT confirmed by mass spectrometry with [M+3H]3+ 1577.33 and [M+3H+K]4+ 1192.88

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.98%

  • 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 · passed · core

    LAL or chromogenic endotoxin assay.

    ≤ 0.05 EU/mL (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

    99.98% purity by HPLC is excellent and normal for research-grade peptides. HPLC chromatogram shows single clean peak at ~14 min.

  • Mass spectrometry confirmation

    Identity confirmed by LCMS/MS with appropriate mass peaks for GLP-RT (retatrutide). Mass spectrum shows expected charge states.

  • Endotoxin testing included

    Separate endotoxin report (page 2, accession 2511190034) shows duplicate testing per USP <85>, both replicates pass at ≤ 0.05 EU/mL.

  • Batch information present

    Lot 0010, net peptide content 12.19 mg stated, white lyophilized powder appearance documented with photo.

  • Lab verification recommended

    Freedom Diagnostics claims USA operation with searchable verification at FreedomDiagnosticsTesting.com. Independent verification of lab credentials and accreditation status recommended.

  • Limited panel scope

    This COA covers purity, identity, and endotoxin only. Heavy metals, microbial contamination, sterility, and residual solvents/water content not tested. This is common for basic peptide COAs but limits comprehensive quality assessment.

  • Professional presentation

    Document includes chromatograms, mass spectra, product photo, signatory (Stephen Schmidt, Principal Chemist), and appropriate research-use-only disclaimers.

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.