Impurity reference standards
Triamterene impurity standards
Zemixal lists 5 reference materials related to Triamterene, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 3 pharmacopoeial impurities and 1 metabolite or hydroxylated analogue.
5reference materials
3pharmacopoeial
1metabolites
Every standard comes with a certificate of analysis. Structure confirmation data, typically NMR, MS and chromatographic purity, is available on request. Laboratories use them to validate related-substance methods, set specification limits under ICH Q3A and Q3B, and identify unknown peaks in stability samples.
By impurity type
Pharmacopoeial3EP, USP, BP or JP named impurities
Metabolites1Hydroxy, desmethyl and conjugated forms
Counts are based on product names. One compound can fall into more than one type.
All Triamterene reference materials
1–5 of 5 standards
Questions
Triamterene impurities, answered
How many Triamterene impurity standards does Zemixal list?
The catalogue currently lists 5 compounds for Triamterene, including 3 pharmacopoeial impurities and 1 metabolite or hydroxylated analogue. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Triamterene 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 Triamterene 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.