Analytical Program
Every batch clears the same six release gates before it is listed for sale. Nothing ships on a supplier's word — it ships on a certificate.
01
Every batch is run on liquid chromatography–mass spectrometry to confirm the observed molecular mass matches the theoretical mass of the sequence. A batch that fails identity confirmation is quarantined and never enters stock.
02
Purity is measured by reverse-phase HPLC with UV detection at 214nm, reported as the area percentage of the main peak. Our release threshold is 99.0%; the exact figure for your batch is printed on the vial and published on the Lab Results page.
03
Fill weight is verified gravimetrically on a calibrated analytical balance, with a sample from each run re-weighed after lyophilisation to confirm the stated milligram content.
04
Each lyophilisate is inspected for colour, cake structure and particulates. Copper complexes should present as a distinct blue cake; all other materials should be white to off-white.
05
Each production run receives a unique batch identifier in the format AUR-XXX-YYMM. That identifier ties the vial in your hand to a specific certificate of analysis — they must match exactly.
06
Lyophilised material is stored at -20°C in nitrogen-flushed, tamper-evident vials with desiccant. Stability is re-checked at six-month intervals for any batch held in long-term stock.
Every released batch and its purity result is published on the Lab Results register. Browse materials by research group in the research catalogue.
All materials are supplied strictly for in-vitro laboratory and research use. They are not medicines, supplements or therapeutic goods, and are not for human or animal consumption.
