Public COA audit

Epithalon

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)
98.8%

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
7yt7grq
Identity method
HPLC-UV-MS
Sample date
2026-02-26
Issue date
2026-03-03

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).

    ID Confirmed

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    98.80%

  • 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.

    <0.5 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 HPLC purity

    98.80% chromatographic purity with 99.2% of label claim (49.6 mg recovered from 50 mg label) is excellent and typical for research-grade peptides.

  • Mass spectral confirmation

    Identity confirmed by HPLC-UV-MS with reference spectrum comparison shown on page 2.

  • Batch/lot number present

    Lot 7yt7grq clearly stated with Lab # 201832 and Project 145100.

  • Dates consistent

    Sample received 2/26/2026, endotoxin tested 2/28/2026, purity/identity tested 3/3/2026, report issued 3/3/2026. All dates are logical and sequential.

  • Lab identification

    Krause Analytical LLC, 8127 Mesa Drive Suite B-206, Austin, TX 78759. Signed by Mark C. Krause, Laboratory Director. Verification URL provided: https://finnrick.com/verify.

  • Endotoxin testing present

    Endotoxin panel present with <0.5 EU result using USP 86 (LAL method), tested 2/28/2026.

  • Heavy metals panel absent

    Methods summary on page 3 describes USP/NF 233 ICP-MS method for metals testing, but no results are reported in this certificate. This may indicate metals testing was not performed for this lot or is reported separately.

  • Microbial and sterility panels absent

    No microbial contamination or sterility testing results are present in this report.

  • Professional presentation

    Document includes chromatogram (page 2), mass spectrum comparison (page 2), detailed methods summary (page 3), and proper watermarking. Formatting is consistent with professional 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.