Originated by Rock Compounds, LLC, which attests it authorized this test as the brand of record.
Axiom confirmed this brand is a registered Axiom account. This does not confirm the product's origin, chain of custody, or that the brand authorized this specific test.
Test Results
| Test | Reference standard | Result | Verdict |
|---|---|---|---|
| Identity | Referencewithin ±1 Da of 1419.556 Da | Result1419.556 Da (error 0 Da) | PASS |
| Purity | Referenceat least 98% (Axiom Analytics internal specification ≥95%) | Result99.77% | PASS |
| Net Peptide Content | Referencewithin ±10% of the 10 mg label claim | Result10.13 mg (+1.34%) | PASS |
| Sterility · Rapid PCR | ReferenceRapid PCR screen | ResultNo Growth | — |
| Endotoxin | Reference≤ 0.5 EU/mg (USP <85>) | Result0.25 EU/mg | PASS |
| Heavy Metals | ReferenceUSP <232>/<233> limits | ResultAll below limits | PASS |
| Stability | ReferencepH within 4.50 - 7.00 and degradation below 5% | ResultpH 5.75, 2.5% degradation at 24 h | PASS |
| Fentanyl Screen | Referenceno fentanyl or analog at or above 1 ng/mg | Resultnone detected | PASS |
Rapid PCR reports a microbial DNA target screen. It is not a USP <71> batch sterility determination.
HPLC Chromatogram
RP-HPLC 214nm (USP 621)Heavy Metals
| Element | Specification | Result | Verdict |
|---|---|---|---|
| Lead (Pb) | ≤ 500 ppb | Not Detected | PASS |
| Arsenic (As) | ≤ 1500 ppb | Not Detected | PASS |
| Cadmium (Cd) | ≤ 200 ppb | Not Detected | PASS |
| Mercury (Hg) | ≤ 300 ppb | Not Detected | PASS |
| Cobalt (Co) | ≤ 500 ppb | Not Detected | PASS |
| Vanadium (V) | ≤ 1000 ppb | Not Detected | PASS |
| Nickel (Ni) | ≤ 2000 ppb | Not Detected | PASS |
Results relate only to the item or portion tested. Unless sampling was performed or witnessed by Axiom Analytics, the laboratory does not attest that the submitted sample represents the wider lot or batch. A PASS designation means only that the reported result met the specification shown. It does not establish safety, efficacy, regulatory approval, legality, or suitability for human or animal use.
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Physical instrument analysis is performed at Axiom Analytics' discretion (based on method, capacity, and order volume), either in Axiom's own laboratory under its documented quality system or by an independent partner laboratory engaged under confidentiality. Where analysis is subcontracted, the method is performed within the partner laboratory's published ISO/IEC 17025 scope of accreditation for that method, not merely at a laboratory holding ISO/IEC 17025 accreditation. Axiom Analytics does not itself currently hold ISO/IEC 17025 accreditation. The method-validation status of each reported result is identified beside that result. Partner laboratory identities are not disclosed: samples are analyzed under double-blind conditions, identified only by an internal lot ID.
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