Public COA audit

Triple Agonist

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
5/7
Purity (printed)
99.85%

Scored high because the document is mostly consistent but carries soft concerns, broad panel coverage (5/7), and 2 soft concerns.

Document details

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

Batch / lot
CR-3XAG-30MG-2606-2
Identity method
HPLC-RTM (retention time match)
Sample date
2026-06-13
Issue date
2026-06-26

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.

5 of 7 present · 5 passed · 0 failed · 0 reported · 2 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.

    99.85%

  • Heavy metals

    Tested · passed

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

    All Not Detected (As, Cd, Cr, Hg, Pb)

  • 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.

    0.096 EU/mL

  • Sterility

    Tested · passed

    Sterility testing where applicable.

    No Growth

  • 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

    99.85% purity by HPLC with conformity testing across 3 samples (mean 99.65%, std dev 0.1633%). This is normal for research peptides.

  • Identity confirmed by HPLC-RTM

    Triple Agonist confirmed via retention time match with reference standard.

  • Batch/lot number present

    CR-3XAG-30MG-2606-2

  • Dates consistent

    Received 2026-06-13, analyzed 2026-06-26, issued 2026-06-26. All dates are on or before 2026-09-05 (today).

  • Lab identified with contact info

    ILS Laboratories, San Diego CA, with phone, address, website, and ISO/IEC 17025 accreditation claim.

  • Verification URL and QR code provided

    portal.ils-lab.com/verify/2qgRtQeSmLEps64L with access code RWJRBNEQ and QR code for authentication.

  • Comprehensive testing suite

    Purity (HPLC), identity (HPLC-RTM), heavy metals (ICP-MS), sterility (PCR), endotoxin (USP <85>), and fentanyl screen all present and passed.

  • Conformity testing performed

    Three samples tested (Dedicated V0, Conformity V1, V2) with statistical analysis (mean, std dev) demonstrating batch consistency.

  • Professional formatting

    Multi-page report with clear tables, chromatogram, methodology notes, and signature. Consistent with professional lab standards.

  • Microbial panel absent

    No traditional microbial testing (TAMC/TYMC) shown. Sterility (PCR) is present but does not replace quantitative microbial enumeration.

  • Residual solvent/water content not tested

    No Karl Fischer water content or residual solvent analysis reported.

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.