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For laboratory research use only. Not for human or veterinary use.
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Documentation
How material is verified before it is listed, how certificates of analysis are produced, and how to read one.
Cryo Reagents does not manufacture. We buy finished lots and then pay an independent laboratory to analyse them, rather than relying on the certificate the manufacturer supplies with the shipment. The laboratory is chosen by us, paid by us, and has no stake in the outcome — which is the only thing that makes a purity figure worth reading.
The analysis is destructive: vials are consumed by the testing and never sold. A lot that arrives without a certificate we commissioned is not listed, and the database refuses to list it — a size cannot be made purchasable until its certificate and lot number are on file.
01
Each lot is received against its manufacturing documentation and held until its paperwork is complete. Nothing is listed as available without a certificate of analysis for that lot.
02
Vials are drawn from the lot and sent to an independent analytical laboratory that we commission and pay. The laboratory has no commercial interest in the result, and no relationship with the manufacturer.
03
The certificate is checked against what arrived: compound, lot number, and stated size. A lot that arrives without a matching certificate is not listed for sale.
04
The certificate is published against the specific lot held in stock and linked from the product page. When stock turns over to a new lot, the certificate on the page changes with it.
The panel we commission covers identity, purity, and net content — what the material is, how much of it is the stated compound, and how much is in the vial.
It does not cover endotoxin, microbial contamination, or elemental impurities. Those are separate determinations we do not currently purchase, and nothing on this site should be read as a claim about them. If that changes, this page changes with it.
| Method | Determines | Notes |
|---|---|---|
| RP-HPLC | Chromatographic purity | Reversed-phase high-performance liquid chromatography separates the sample by hydrophobicity. Purity is reported as the area of the main peak as a percentage of total peak area at the stated wavelength. |
| Mass spectrometry | Identity | The observed molecular mass is compared against the theoretical mass for the sequence or formula. A match within instrument tolerance confirms the material is what the label says. |
| Karl Fischer or loss on drying | Water content | Residual water in a lyophilised solid. This matters because a stated net peptide mass is otherwise ambiguous. |
| Appearance and solubility | Physical conformity | Visual inspection against the expected form, colour, and dissolution behaviour. |
A certificate of analysis records what a laboratory measured, on a specific lot, on a specific date, using a stated method. It describes the material and nothing else. It is also a document produced by a party with an interest in the result, which is why the chromatogram and the mass spectrum matter more than the summary figures. Read it field by field:
If a certificate and a vial disagree, or a figure looks wrong, contact us with the order number and lot number before using the material.