Quality & Analytics
Rigorous analytical testing is not an afterthought; it is the core of our offering. We verify identity and purity so you can trust your experimental data.
Our Analytical Approach
Two core analytical methods underpin our approach to peptide quality. The methods applied to a given product are scoped and confirmed per enquiry:
Chromatographic Purity (HPLC)
Reverse-phase High-Performance Liquid Chromatography can separate the target peptide from synthesis byproducts and truncations. Where HPLC is part of the agreed analytical scope, the applicable result and documentation are confirmed for the requested lot.
Molecular Identity (LC-MS)
Liquid Chromatography-Mass Spectrometry is used to confirm the molecular mass of the principal peak against the intended sequence, with the result recorded in the batch documentation.
Our Quality Pillars
HPLC Purity Analysis
Reverse-phase high-performance liquid chromatography can be applied to assess purity. The analytical methods applied to a given product are scoped per enquiry, with results documented in the certificate of analysis for that lot where provided.
Mass Spectrometry Identity Testing
LC-MS can be used to confirm the molecular identity of a peptide against the intended sequence. Whether it is included for a given lot is confirmed per product and enquiry, with results recorded in the batch documentation supplied.
Batch Certificates of Analysis
Batch documentation covering parameters such as purity, identity, appearance, and net content can be provided on request. The documentation available for a given lot is confirmed per enquiry.
Lyophilized Stability
Peptides are typically freeze-dried into a lyophilized powder. Vial and packaging specifications are confirmed per product and enquiry to support stability in storage and transit.
Storage & Shipping
Storage guidance and shipping arrangements, including any temperature-control and tracking requirements, are scoped and confirmed per order in the transaction documents.
Documented Process Controls
Manufacturing follows documented process controls. The specific controls, records, and traceability applicable to a given product are confirmed per enquiry.