Reference-standard peptides.
cGMP-Audited Synthesis
HPLC / MS Characterised
SDS and CoA Per Lot
EU Institutional Supply
cGMP-Audited SynthesisHPLC / MS CharacterisedSDS and CoA Per LotEU Institutional Supply
The Science
01Purpose
Reference-standard supply
endopep supplies analytical-grade synthetic peptides as reference standards to qualified research institutions across the European Union. Every substance is synthesised under cGMP-audited conditions, characterised lot-by-lot, and documented to laboratory-supply standards.
02Characterisation
Identity, purity, lot integrity
Every lot is released against an internal specification verified by HPLC for purity, mass spectrometry for identity, Karl-Fischer titration for residual water, and LAL assay for endotoxin. A Safety Data Sheet is provided for each substance.
03Documentation
Transparent and auditable
Every substance is released against a published specification. Safety Data Sheets are compiled per REACH Annex II and retained in accordance with REACH Article 36. Nothing in the catalogue is supplied without a release document.
04Supply
Qualified recipients only
Supply is restricted to professional research institutions verified during account review. Shipping is to institutional addresses within the European Union. The catalogue is not available to consumers and is not sold for therapeutic, personal, food, cosmetic, diagnostic, or veterinary purposes.
05Classification
Intended use is in-vitro research
These substances are reference standards for in-vitro laboratory research. They are not medicinal products, are not authorised for human or veterinary administration, and are not intended for in-vivo use by any route. Any other use is a breach of the Acceptable Use Policy and terminates supply.
Catalogue
Selected reference standards
Catalogue updates.
New reference standards, lot release notices, and documentation updates. For qualified researchers only.
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