Public COA audit
Triple Agonist
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
- 3/7
- Purity (printed)
- 99.82%
Scored moderately because the document is mostly consistent but carries soft concerns, limited panel coverage (3/7), 3 soft concerns, and notable note: "High purity confirmed". To improve: include identity, purity, and endotoxin at minimum.
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- CRRT-30-0310-1
- Identity method
- LCMS/MS (HPLC with UV Detection Coupled with Mass Spectrometry)
- Sample date
- 2026-03-17
- Issue date
- 2026-03-18
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.
3 of 7 present · 3 passed · 0 failed · 0 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).
GLP RT confirmed
Purity
Tested · passed · core
Reported purity percentage for the analyte.
99.82% average (Vial 1: 99.84%, Vial 2: 99.79%, Vial 3: 99.82%)
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.
≤ 0.05 EU/mL (both replicates)
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
Average purity of 99.82% across three vials is excellent and consistent with high-quality research peptides. HPLC chromatogram shows clean single peak.
Mass spec confirmation present
Mass spectrometry data shows expected molecular ion peaks ([M+3H]3+ at 1577.85 and [M+3H+K]4+ at 1192.85), confirming peptide identity.
Endotoxin testing included
Endotoxin testing performed with two replicates, both passing at ≤ 0.05 EU/mL threshold.
Lab verification unclear
Freedom Diagnostics website (FreedomDiagnosticsTesting.com) and verification system cannot be independently confirmed. Lab claims USA operation but provides limited accreditation information.
Professional presentation with minor inconsistencies
Document has professional layout with logo, tables, and chromatograms. However, some formatting elements (e.g., 'TEST TEST TEST' watermarks at top) are unusual for final COAs.
Batch information complete
Lot number CRRT-30-0310-1 clearly stated with individual vial content measurements (36.80 mg, 35.02 mg, 34.35 mg).
Dates appropriate
Received 03/17/2026, reported 03/18/2026 - one-day turnaround is reasonable for routine testing.
Limited testing scope
COA only includes purity, identity, and endotoxin testing. Missing heavy metals, microbial, sterility, and residual solvent/water content panels that some vendors provide.
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.