Impurity reference standards
Diclazuril impurity standards
This page brings together 10 Diclazuril related compounds that analytical teams use to identify, quantify and control impurities in the active ingredient and the finished dosage form. The range includes 9 pharmacopoeial impurities.
10reference materials
9pharmacopoeial
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. Typical uses are method development and validation, relative response factor work, forced degradation studies and the impurity sections of ANDA, DMF or CEP filings.
By impurity type
Pharmacopoeial9EP, USP, BP or JP named impurities
Counts are based on product names. One compound can fall into more than one type.
All Diclazuril reference materials
1–10 of 10 standards
Questions
Diclazuril impurities, answered
What Diclazuril reference materials are available?
The catalogue currently lists 10 compounds for Diclazuril, including 9 pharmacopoeial impurities. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Diclazuril 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 Diclazuril 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.