Public COA audit

Oxytocin

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
72
Confidence
85%
Panels
1/7

Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (1/7), 2 soft concerns, and notable note: "Endotoxin-only report". To improve: include identity, purity, and endotoxin at minimum.

Document details

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

Batch / lot
B-1340958-E
Sample date
2026-05-27

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.

1 of 7 present · 1 passed · 0 failed · 0 reported · 6 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

    Tested · passed · core

    LAL or chromogenic endotoxin assay.

    <0.06 EU/mL

  • 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.

  • Endotoxin-only report

    This is an endotoxin-specific COA (lot suffix -E). The document clearly states 'Endotoxin Test' and reports <0.06 EU/mL, which is a passing result. This appears to be a split report focused solely on endotoxin testing.

  • No purity or identity data

    This report contains only endotoxin testing. No HPLC purity, MS identity, or other analytical panels are present. This is typical for split reports where purity/identity may be documented separately (e.g., lot B-1340958-P).

  • Lot number present

    Lot B-1340958-E clearly identified with -E suffix indicating endotoxin-focused testing.

  • Dates within valid range

    Received date 06/01/2026 and analysis conducted 05/27/2026. The received date is after the analysis date, which is unusual but may reflect data entry or reporting workflow. Both dates are on or before the current date (2026-09-05).

  • Analysis before receipt

    Analysis conducted date (05/27/2026) precedes the received date (06/01/2026) by 5 days. This temporal inconsistency may indicate a data entry error or unusual workflow.

  • Lab identification

    Horizon Analytical identified with contact email and verification URL. Signed by Aleksey Yevtodiyenko PhD, Research and Formulation Chemist.

  • Professional presentation

    Document includes QR code for validation, professional layout, compound metadata (CAS, formula, molecular weight, PubChem CID), and signature.

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.