Public COA audit

Selank

Audited September 5, 2026

Consistent with a legitimate COA

Document structure and test panels align with what we expect from authentic lab reports.

Legitimacy
95
Confidence
95%
Panels
5/7
Purity (printed)
99.67%

Scored high because document structure and panels look consistent with authentic lab output and broad panel coverage (5/7).

Document details

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

Batch / lot
CR-SLK5-2605-1
Identity method
HPLC-RTM (retention time match)
Sample date
2026-05-22
Issue date
2026-06-01

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.

Loading original certificate…

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 · 4 passed · 0 failed · 1 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 (Selank)

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.67% (mean 99.66%, n=3)

  • 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 · result on file · core

    LAL or chromogenic endotoxin assay.

    NMT 0.05 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 with triplicate testing

    99.67% purity (mean 99.66%) confirmed across three samples (Dedicated V0, Conformity V1, V2) with low standard deviation (0.0047%), demonstrating excellent batch consistency.

  • Identity confirmed by HPLC retention time

    Selank identity confirmed by HPLC-RTM (retention time match) with reference standard. Chromatogram shows expected peak profile.

  • Comprehensive testing panel

    Full QC panel includes purity/quantitation (HPLC), identity (HPLC-RTM), heavy metals (ICP-MS), sterility (PCR), endotoxin (USP <85>), and fentanyl screening. Five of seven standard panel types present.

  • Clear batch identification

    Lot number CR-SLK5-2605-1, COA number COA-2026-TEHYON, Accession ACC-2026-3099. All identifiers clearly stated.

  • Dates are consistent and valid

    Sample received 2026-05-22, analyzed 2026-06-01, issued 2026-06-01. All dates are on or before 2026-09-05 (today) and show reasonable turnaround time (10 days).

  • ISO/IEC 17025 accredited lab

    ILS Laboratories, San Diego, CA. Document states ISO/IEC 17025 accreditation. Verification URL and QR code provided (portal.ils-lab.com/verify/P1SUxKNXG44ClNv5). Access code CR9T6MKD.

  • Endotoxin testing present

    Endotoxin tested per USP <85> kinetic turbidimetric method. Result: NMT 0.05 EU/mL. Document notes this is below commonly referenced thresholds and that no universal pass/fail applies to RUO products.

  • Professional multi-page format

    Three-page COA with consistent branding, clear tables, HPLC chromatogram, methodology notes, and lab director signature. Professional presentation consistent with accredited lab standards.

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.