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Impurity reference standards

Emtricitabine impurity standards

Zemixal lists 32 reference materials related to Emtricitabine, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 2 metabolites or hydroxylated analogues and 1 degradation product.

32reference materials
2metabolites
1degradants
Emtricitabine WS structure
Parent API

Emtricitabine WS

CAS
143491-57-0
Formula
C8H10FN3O3S
MW
247.25 g/mol
Code
ZX-006528

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. 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

Metabolites2Hydroxy, desmethyl and conjugated forms
Degradants1N-oxides, dimers, lactones and breakdown products

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

All Emtricitabine reference materials

1–32 of 32 standards
Questions

Emtricitabine impurities, answered

How many Emtricitabine impurity standards does Zemixal list?
The catalogue currently lists 32 compounds for Emtricitabine, including 2 metabolites or hydroxylated analogues 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 Emtricitabine 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 Emtricitabine 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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