Pharmaceutical Impurities Standard (2 components)
- Features two common alkyl halides—chloromethane and chloroethane—that can form during drug synthesis.
- High-concentration (5,000 μg/mL) solution maximizes flexibility; ideal for analyzing pharmaceutical genotoxic impurities (GTIs).
- Quantitatively tested to confirm composition and stability; detailed support documentation provided.
Certified reference materials (CRMs) manufactured and QC tested in ISO-accredited labs satisfy your ISO requirements.