Public COA audit

Tesamorelin

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
88
Confidence
87%
Panels
2/7
Purity (printed)
99.301%

Scored high because the document is mostly consistent but carries soft concerns, limited panel coverage (2/7), 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
TS20250722
Identity method
HPLC retention time and spectral match
Issue date
2025-08-22

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.

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

    RT match 1.00-1.01, Spectral match 1000

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.104% and 99.301%

  • 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.

  • High purity confirmed

    Two vials tested at 99.104% and 99.301% purity by HPLC, both within normal range for research-grade peptides

  • Identity confirmed by dual methods

    Retention time match (1.00-1.01) and spectral match (1000) both confirm Tesamorelin identity

  • Assay quantification provided

    Vials contain 9.880 mg and 10.430 mg, close to labeled 10mg claim

  • Batch/lot number present

    Client SID TS20250722 clearly stated

  • Sample date not stated

    Published date 2025-08-22 is present but no explicit sample receipt or collection date

  • Lab identification complete

    TrustPointe Analytics LLC with full address, phone, email, website, and verification URL with key XF9S0WK37A00

  • Purity/identity-scoped report

    This COA covers purity and identity testing only. Heavy metals, microbial, endotoxin, sterility, and residual solvent panels are not included in this report. This is common for split testing where additional safety panels may be documented separately.

  • Professional presentation

    Document includes QR code, dual signatures (President and Managing Director), system suitability data (1.8% RSD), coelution control, and photo attachment of tested vials

Timing & next steps

Practical follow-ups based on document age and gaps.

  • coa age

    This COA was issued over a year ago (379 days) — consider whether a retest is warranted for this batch.

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.