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Certificates of Analysis available upon request.
The Aurevra Bio standard, written in detail. Every claim we make is one we are prepared to back with batch-specific evidence.
Standards last reviewed 2026-06-30 · Version 1.0
≥98%
Minimum HPLC purity
Measured per batch, not asserted as a floor.
6
Quality checkpoints
Identity through shipping — documented below.
On request
Certificate of Analysis
support@aurevrabio.com · ≤1 business day.
Every compound is identified by name, CAS Registry Number, molecular formula, and molecular weight on its product page and on every COA.
Where a sequence is published, we list it. Where a synthesis route matters, we name the methodology. No abbreviations without expansion.
Every batch is verified by High-Performance Liquid Chromatography. The minimum purity standard is ≥98%. The COA reports the actual measured value for the specific batch — not a generic threshold claim.
Methodology is reverse-phase HPLC with a UV detector. The methodology section of the COA lists the column, mobile phase, gradient, flow rate, and wavelength used. Our claims are reproducible.
Illustrative purity trace — actual results are batch-specific and reported on the COA
Every lot is documented with a Certificate of Analysis identifying compound, batch number, manufacture date, measured purity, and methodology. The COA records compound identity verification, HPLC purity measurement, and the analytical conditions used to verify it.
Certificates of Analysis are available upon request — email support@aurevrabio.com with the compound name and (where applicable) your order number. Past-batch COAs are retained for audit and chain-of-custody documentation.
Synthetic peptides degrade with heat exposure. Every order ships with insulated packaging, gel ice packs, and discrete outer cartons. For transit windows over 48 hours, dry-ice is used.
The cold-chain protocol is part of what the COA covers — purity at the point of testing is only meaningful if the compound is handled correctly from that point forward.
Every account holder accepts the Research Use Only terms at registration. Every order captures an acknowledgment with a timestamp and recorded acceptance.
We do not solicit consumers. We do not provide protocols. We do not make efficacy claims.
We work with a vetted contract manufacturing organization and an independent third-party analytical lab. The supplier-specific identification will be published on this page once vendor agreements permit named disclosure — in the interim, lot-specific references are available on request alongside the corresponding Certificate of Analysis.
Researchers requiring institutional documentation may contact us at support@aurevrabio.com for full supplier disclosure under NDA.