Quality & Testing
Quality & Testing
How we describe documentation and analytical information — accurately, per product, without claims we cannot substantiate.
Our principle
Research materials should be assessed on clear specifications and accessible documentation, not on broad quality language. Our policy is to describe analytical and quality documentation for each product on the basis of what is actually available for that item, and to provide that documentation on request. We do not apply uniform testing claims across the catalogue.
What documentation can include
- Identification. Confirmation of compound identity, commonly supported by mass spectrometry where applicable.
- Purity assessment. A purity figure against a stated method, commonly high-performance liquid chromatography (HPLC) where applicable.
- Lot reference. A batch/lot identifier linking an order to its documentation.
Plain-language explanations of these methods are in the Analytical Methods Overview.
Process
From product identification to fulfilment
Product Identification
Compound, catalogue ID, form and nominal quantity stated on every listing.
Analytical Information
Described where applicable to the product; not asserted uniformly. [Verify]
Documentation Availability
CoA and product documentation available on request by catalogue ID.
Batch / Lot Process
Lot referencing where applicable for traceability and re-ordering.
Fulfilment & Communication
Stock and dispatch expectations communicated as part of the order.
Need documentation for a specific product?
Quote the catalogue identifier and our team will confirm what is available.
Request Documentation