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Impurity reference standards

Sibutramine impurity standards

For Sibutramine, the Zemixal catalogue holds 11 impurity and reference standards that support release testing, stability programmes and regulatory dossiers. Counted by type, there are 2 metabolites or hydroxylated analogues.

11reference materials
2metabolites

Every standard comes with a certificate of analysis. Structure confirmation data, typically NMR, MS and chromatographic purity, is available on request. They are bought for system suitability, peak identification, quantitation against limits and the impurity justification sections of regulatory submissions.

By impurity type

Metabolites2Hydroxy, desmethyl and conjugated forms

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

All Sibutramine reference materials

1–11 of 11 standards
Questions

Sibutramine impurities, answered

What Sibutramine reference materials are available?
The catalogue currently lists 11 compounds for Sibutramine, including 2 metabolites or hydroxylated analogues. Each product page shows the CAS number where one is assigned, the structure, formula and molecular weight.
What documents come with a Sibutramine 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 Sibutramine 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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