Public COA audit
IPAMORELIN
Audited September 5, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 72
- Confidence
- 85%
- Panels
- 2/7
- Purity (printed)
- 99.83%
Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (2/7), 3 soft concerns, and notable note: "High purity reported". To improve: include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- IPA10N050525
- Identity method
- Assessment of a peptide vial or vials
- Sample date
- 2025-05-13
- Issue date
- 2025-05-14
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.
2 of 7 present · 0 passed · 0 failed · 2 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 · result on file · core
Compound identity confirmed (e.g. HPLC, mass spec).
11.53 mg; 11.55 mg; 11.51 mg
Purity
Tested · result on file · core
Reported purity percentage for the analyte.
99.767%; 99.860%; 99.830%
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 reported
Three measurements showing 99.767%, 99.860%, and 99.830% purity. High purity is normal for research peptides and not inherently suspicious.
Mass measurements provided
Three vial measurements reported: 11.53 mg, 11.55 mg, 11.51 mg, showing consistency across samples.
Batch number present
Batch IPA10N050525 clearly stated
Dates consistent and valid
Testing ordered 09 MAY 2025, sample received 13 MAY 2025, analysis conducted 14 MAY 2025. All dates are sequential and on or before 2026-09-05.
Known testing laboratory
Janoshik is a recognized third-party peptide testing laboratory with verification system
Verification URL provided
Unique verification key CH8F1F9EW44K provided with URL www.janoshik.com/verify/
Limited testing scope
This report covers only identity and purity testing. No heavy metals, microbial, endotoxin, sterility, or residual solvent testing included in this specific report.
Minimal detail on methodology
Test description is generic ('Assessment of a peptide vial or vials'). No specific analytical method details (e.g., HPLC conditions, column type) provided on this page.
No pass/fail criteria stated
Results are reported numerically but without explicit pass/fail determination or specification limits
Timing & next steps
Practical follow-ups based on document age and gaps.
coa age
This COA was issued over a year ago (479 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.