Impurity reference standards
Novoldiamine impurity standards
This page brings together 2 Novoldiamine related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. Most entries are process-related impurities, synthesis intermediates and isomers.
2reference materials
Batches are supplied with a certificate of analysis, and the supporting spectra can be sent ahead of a purchase order so your QA team can review them. They are bought for system suitability, peak identification, quantitation against limits and the impurity justification sections of regulatory submissions.
All Novoldiamine reference materials
1–2 of 2 standards
Questions
Novoldiamine impurities, answered
What Novoldiamine reference materials are available?
The catalogue currently lists 2 compounds for Novoldiamine. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Novoldiamine impurity standard?
A certificate of analysis travels with every lot. On request we share the characterisation set, usually 1H-NMR, mass spectrum, HPLC purity and IR, and for some materials TGA or water content. Ask for the data before ordering if your QA team needs to review it.
Can Zemixal make a Novoldiamine impurity that is not listed?
Often yes. Send the structure, name or CAS number with the quantity you need and our sourcing team checks custom synthesis options, usually from 10 mg up to gram scale, with a quoted lead time.