We report net peptide content, not just purity — so the milligrams you dose aren't padded with water and counter-ion. RP-HPLC purity and ESI-MS identity, on a lot-numbered COA.
Net peptide content, not just purity — RP-HPLC + ESI-MS, lot-numbered COA.
Net peptide content on every lot's COA.
Reading a Peptide HPLC Trace — A 5-Minute Field Guide for Bench Scientists. Read our briefing →
Reading a peptide HPLC trace — a field guide. Read →
On reading HPLC traces. Read →
Reference-name product · composition documented per batch
Lyochem buyer fit
This Lyochem page is intentionally written for research labs, core facilities, and method-development teams qualifying ADMAX Research Preparation as a reference-grade lot. It is not the pharmacy procurement owner for this SKU; the page should win differentiated searches around sequence verification, assay suitability, lot continuity, and data-packet depth.
Overview
ADMAX is a trade-name preparation carried in upstream-manufacturer price tables without a publicly resolved API identity; the name conventionally denotes a defined-process preparation rather than a single defined molecule. It surfaces chiefly across Russian and Eastern European supplier listings, an ecosystem where labelling products by reference name is a long-established commercial convention. Following standard practice for all reference-name SKUs, its composition, sequence and CAS designation are established from the batch-specific Certificate of Analysis — checked at order placement and re-checked on batch receipt — rather than assumed from the label. Lyochem carries ADMAX to accommodate research-buyer workflows built around upstream-supplier price references. For direct end-buyers, the operative record is the COA's component-level analysis, which reflects the verified composition of the released material; the trade name alone should never be treated as adequate documentation for downstream regulatory or quality purposes. Buyers needing explicit composition disclosure ahead of ordering should engage the regulatory team.
Applications & buyer fit
Khavinson short bioregulators — Admax, Cortagen, Cartalax, Cardiogen, Bronchogen, Crystagen, Prostamax, Vesugen — ship to research labs replicating Russian-school protocols or running comparative tissue-specific peptide-bioregulator studies. The published literature base for this class is concentrated in Russian-language sources; buyers should expect to consult that literature directly for protocol selection. Analytical-packet expectations are the same as any other lyophilised research peptide.
Contract Research Organisations (CROs)
CROs running preclinical and translational studies on behalf of academic, biotech, or pharma sponsors who need traceable reference material across multi-site campaigns.
Every release ships with its own batch-specific CoA — identity, purity, and the analytical scope agreed at quote stage, tied to the exact lot you receive.
Review a representative batch CoA before you order, so you can confirm the packet matches what your method or sponsor audit needs.
Supplied strictly as a research reagent to research institutions — not a finished dosage form and not for human administration. Buyer qualification runs at the inquiry stage.
Specifications
Documentation available on request
Regulatory note
A reference-name preparation whose API identity is not publicly disclosed; ahead of any downstream research or regulatory use, its composition is recorded on the batch-specific COA.
Frequently asked questions
Because the formulation is held by the upstream manufacturer, the batch analysis characterizes the released material as-is rather than deconstructing the recipe. RP-HPLC gives the chemical-purity profile of the preparation and fingerprints the dominant species, while mass-spec confirms the mass of that dominant species for batch-to-batch comparison. Karl Fischer reports water content, and USP <61>/<62> microbial limits cover finished-product-grade use, with LAL endotoxin testing per USP <85> available on request for injectable workflows. This gives a reproducible identity fingerprint and quality baseline even though the proprietary composition is not independently re-characterized.
The practical value of the packet is comparability. By retaining the RP-HPLC chromatogram and the mass of the dominant species from a qualified lot, a buyer establishes a reference fingerprint that later batches can be checked against, so drift in the chromatographic profile becomes visible even without full composition disclosure. If a documentation chain requires the underlying identity, the recommended path is to obtain the named-API disclosure and qualify that SKU instead. For buyers who must stay with the reference-name product, archiving each lot's COA and chromatogram preserves the traceability their quality system needs.