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Impurity reference standards

Pheniramine impurity standards

Zemixal lists 6 reference materials related to Pheniramine, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 3 pharmacopoeial impurities and 1 degradation product.

6reference materials
3pharmacopoeial
1degradants

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.

By impurity type

Pharmacopoeial3EP, USP, BP or JP named impurities
Degradants1N-oxides, dimers, lactones and breakdown products

Counts are based on product names. One compound can fall into more than one type.

All Pheniramine reference materials

Questions

Pheniramine impurities, answered

How many Pheniramine impurity standards does Zemixal list?
The catalogue currently lists 6 compounds for Pheniramine, including 3 pharmacopoeial impurities and 1 degradation product. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Pheniramine 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 Pheniramine 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.
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