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Impurity reference standards

Lamivudine impurity standards

Zemixal lists 26 reference materials related to Lamivudine, covering the drug substance itself, its process impurities and the products it forms on storage. Among them are 8 pharmacopoeial impurities and 3 metabolites or hydroxylated analogues.

26reference materials
8pharmacopoeial
3metabolites
Lamivudine structure
Parent API

Lamivudine

CAS
134678-17-4
Formula
C8H11N3O3S
MW
229.26 g/mol
Code
ZX-006595

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. 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

Pharmacopoeial8EP, USP, BP or JP named impurities
Metabolites3Hydroxy, desmethyl and conjugated forms

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

All Lamivudine reference materials

1–26 of 26 standards
Questions

Lamivudine impurities, answered

How many Lamivudine impurity standards does Zemixal list?
The catalogue currently lists 26 compounds for Lamivudine, including 8 pharmacopoeial impurities and 3 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 Lamivudine 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 Lamivudine 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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