Independent Analytical Testing
for Research Compounds.
Publicly verifiable Certificates of Analysis for peptide purity, identity, endotoxins, heavy metals, and batch-level quality verification — performed by an independent third-party laboratory.
Verification built for research accountability.
Every test follows documented methodology and produces a structured Certificate of Analysis with a publicly verifiable accession number.
Quantitative purity testing using high-performance liquid chromatography.
Mass spectrometry confirmation to verify compound identity.
Testing for bacterial endotoxins and microbial contamination indicators.
Screening for metals, residual solvents, and other analytical quality markers.
Public COA Lookup
Verify a Certificate of Analysis using the Search Code or Accession Number printed on the document. Records are accessed individually — no public listing of submitters.
Codes are not case-sensitive. Remove any spaces.
- 1Locate your Certificate of Analysis document.
- 2Find the Search Code field in the top right of the COA header.
- 3Enter that code into the lookup field above and click Look up.
Structured methodology, transparent inputs.
Every panel maps to documented compendial methods. Results are reported with detection range, method reference, and acceptance criteria.
| Test | Description | Reference | Detection Range |
|---|---|---|---|
| HPLC Purity | Quantitative purity analysis | USP-aligned | 0.05 – 100% |
| LC-MS Identity | Molecular mass confirmation | ESI-QTOF | ± 5 ppm |
| Bacterial Endotoxin | Kinetic chromogenic LAL · USP <85> | 405 nm | 0.01 – 1.0 EU/mL |
| Heavy Metals | ICP-MS multi-element screen | USP <232/233> | ppb range |
| Microbial / Sterility | Contamination indicator panel | USP <61> | TAMC · TYMC |
| Residual Solvents | Headspace GC-FID | USP <467> | Class 1/2/3 |
What every Axiom COA includes.
Every certificate is built around a standardized structure so results are unambiguous, comparable across batches, and independently verifiable.
Built for vendors, researchers, and quality verification.
Provide your customers with independent, third-party verification of compound identity, purity, and quality.
Researchers and reviewers can confirm any COA against the originating sample using a public accession number.
Track quality across lots and batches with consistent methodology and reportable acceptance criteria.
From sample receipt to public verification.
Complete the submission form and ship the material with required handling notes.
Each sample is logged into the registry and assigned a unique accession ID.
Selected panels are executed against documented compendial methods.
Final certificate is published with a QR-verifiable lookup record.
Request analytical testing.
Submit a sample for purity, identity, endotoxin, or quality verification testing. Our team will respond with intake instructions and an accession number.
All inquiries are handled through the contact form — no phone or email intake.