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Impurity reference standards

Terazosin impurity standards

For Terazosin, the Zemixal catalogue holds 16 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 13 pharmacopoeial impurities and 1 nitrosamine.

16reference materials
13pharmacopoeial
1nitrosamines

Each lot ships with a certificate of analysis, and characterisation data such as 1H-NMR, mass spectrum and HPLC purity can be shared before you order. Laboratories use them to validate related-substance methods, set specification limits under ICH Q3A and Q3B, and identify unknown peaks in stability samples. For nitrosamine risk evaluation, the N-nitroso standards allow confirmatory LC-MS testing against the acceptable intake limits.

By impurity type

Pharmacopoeial13EP, USP, BP or JP named impurities
Nitrosamines1N-nitroso impurities for ICH M7 work

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

All Terazosin reference materials

1–16 of 16 standards
Questions

Terazosin impurities, answered

What Terazosin reference materials are available?
The catalogue currently lists 16 compounds for Terazosin, including 13 pharmacopoeial impurities and 1 nitrosamine. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Terazosin 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 Terazosin 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.
Do you supply Terazosin nitrosamine impurities?
Yes. 1 N-nitroso compound is listed for Terazosin. They are used for confirmatory testing and method validation in line with ICH M7 and the nitrosamine guidance from the major regulators.
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