Public COA audit

KLOW Blend (TB-500 + BPC-157 + KPV + GHK-Cu) · TB-500

Audited September 3, 2026

Mostly consistent, with concerns

Several fields check out, but we found issues worth reviewing before you rely on this document.

Legitimacy
72
Confidence
83%
Panels
3/7
Purity (printed)
99.7%

Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (3/7), 4 soft concerns, and notable note: "High HPLC purity reported". To improve: include identity, purity, and endotoxin at minimum and prefer labs with a public verification portal.

Document details

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

Batch / lot
78928
Identity method
MS (Mass Spectrometry)
Issue date
2026-06-02

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 · 2 passed · 0 failed · 1 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).

    Conforms

  • Purity

    Tested · passed · core

    Reported purity percentage for the analyte.

    99.7%

  • 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

    Tested · result on file

    Residual solvents or water content limits.

    1.62% acetic acid

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 reported

    99.7% purity by HPLC is within normal range for research peptides and is supported by identity confirmation via MS

  • Identity verification present

    MS fingerprint confirmation for each component of the blend reported as conforming

  • Batch information complete

    Lot number 78928 with manufacturing date June 2, 2026 and retest date June 2, 2028

  • Issue date valid

    Issue date of June 2, 2026 is on or before the current date of September 3, 2026

  • Lab verification not possible

    Novo Pharmaceutical Co., Ltd. is not a widely recognized third-party testing laboratory. No verification URL or contact information provided to independently confirm authenticity

  • Limited testing scope

    COA lacks heavy metals, microbial, endotoxin, and sterility testing. While not uncommon for research-grade peptides, more comprehensive testing would increase confidence

  • Generic presentation

    Document uses generic certification badges (GMP, ISO, QOA) without specific accreditation numbers or verifiable credentials beyond the ISO 9001:2015 reference

  • Manufacturer as testing lab

    The COA appears to be issued by the manufacturer rather than an independent third-party laboratory, which reduces objectivity

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.