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.
- L1Identity
- L2Chromatographic & Carrier Purity
- L3Declared Content
- L4Sterility
- L5Endotoxin
- L6Heavy Metals
- L7Physicochemical Properties
More views of Vial A
Test Results
Select a test for its full result| Test | Reference standard | Result | Verdict |
|---|---|---|---|
| Referenceretention time corresponds to the reference standard run on the same sequence | Resultretention-time correspondence with the reference standard confirmed; the two retention times were not recorded | PASS | |
| ReferenceExpected not less than 99.5 · Acceptance NLT 99.5 % area · Units % area · Source Kovera Labs Bacteriostatic Water Analysis KVR-2026-4784C8 (third-party lab COA; sha256 47c9d3eedafebf3c0eef2d901353766453b12734b2819867b93e02ecd4fdfd6c), Benzyl Alcohol Assay (GC) table row 4: "Purity (GC) ≥ 99.5%". Scope: a bacteriostatic WATER sample. | Result99.87% | PASS | |
| Reference80-120% of the frozen label claim; stored percentage must equal measured content / declared content × 100; USP <341> system suitability and traceability required | Result0.9 % w/v · 100% of the 0.9% w/v label claim | PASS | |
| ReferenceRapid PCR screen | ResultTarget DNA not detected | PASS | |
| Reference< 0.5 EU/mL (USP <85>) | Result0.052 EU/mL | PASS | |
| ReferenceUSP <232>/<233> limits | ResultAll below limits | PASS | |
| ReferencepH within 4.50 - 7.00 | ResultpH 5.78 | PASS | |
| Referencecolorless; clear; free from visible particles | Resultcolorless; clear; no visible particles observed | PASS |
REPORTING SCOPE & LIMITATIONS
- [Chromatographic & Carrier Purity]The chromatographic trace was not retained for this certificate. The purity value and its acceptance limit are unaffected.
- [Sterility · Rapid PCR]DNA-target research screen only. It detects microbial DNA from viable and non-viable organisms alike, and is neither viable-CFU enumeration under USP <61> nor a batch sterility determination under USP <71>.
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.
All analytical testing, validation reports, and interactive Certificates of Analysis (COAs) provided by Axiom Analytics are intended strictly for Research Use Only (RUO) in in-vitro or laboratory animal model environments. Axiom Analytics does not analyze, validate, evaluate, or make any representations regarding the safety, efficacy, toxicity, or legality of any tested substance for human or animal consumption, veterinary use, clinical diagnostics, food additives, cosmetics, or household applications.
Physical instrument analysis is performed within Axiom Analytics' laboratory network, allocated at Axiom's discretion based on method, capacity, and order volume. Axiom Analytics performs sample accession, chain of custody, analytical oversight, and data review, and issues and is responsible for this certificate. 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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