Public COA audit
Selank
Audited July 28, 2026
Missing panels or key metadata — not enough evidence to treat this as a full certificate.
- Legitimacy
- 35
- Confidence
- 88%
- Panels
- 0/7
Scored poorly because the file is incomplete or not a full COA, limited panel coverage (0/7), 3 critical findings, and notable note: "Only assay test present". To improve: upload the full certificate (or the matching sibling purity/endotoxin report) and include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- N260710-001
- Issue date
- 2026-07-17
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.
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.
0 of 7 present · 0 passed · 0 failed · 0 reported · 7 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
Not on this certificate file · core
Compound identity confirmed (e.g. HPLC, mass spec).
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.”
Purity
Not on this certificate file · core
Reported purity percentage for the analyte.
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.”
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
Not on this certificate file · core
LAL or chromogenic endotoxin assay.
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.”
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.
Only assay test present
COA contains only a single HPLC assay test (10 mg specification vs 11 mg result). No identity confirmation, purity percentage, heavy metals, microbial, endotoxin, sterility, or residual solvent/water testing is documented.
No purity data
The HPLC test reports only an assay (mass/quantity: 10 mg spec vs 11 mg result), not a purity percentage. For peptide research, purity by HPLC is a fundamental quality parameter and is absent.
No identity confirmation
No identity testing (MS, NMR, or other method) is documented. Cannot confirm the material is actually Selank.
No sample/test date
Issue date is 2026-07-17, but no sample collection date or test date is provided. Cannot verify when the material was actually analyzed.
Cannot verify lab accreditation
Qalitex Inc. claims ISO/IEC 17025:2017 accreditation (AGS-US050824-1) but no verification URL or QR code link is provided. The accreditation number format is non-standard and cannot be independently verified.
Minimal content for 2-page document
Page 2 is essentially blank except for a footer statement. Legitimate multi-page COAs typically contain additional test data, chromatograms, or detailed methodology on subsequent pages.
Batch identifiers present
Batch number N260710-001 and lot number SP26-SLV10 are clearly documented.
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.