Impurity reference standards
Vancomycin impurities & reference standards
Characterised Vancomycin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
16reference materials
1nitrosamine impurities
COAHPLC · NMR · MS on request
Vancomycin EP Impurity E (Vancomycin CDP-1) (Mixture of two atropisomers)
- CAS
- 55598-85-1
- Formula
- C66H74Cl2N8O25
- MW
- 1450.2 g/mol
VQ-044729
FAQs — Vancomycin impurities
Which Vancomycin impurities do you supply?
We list 16 Vancomycin-related reference materials, including process impurities, degradation products, nitrosamine impurities and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Vancomycin impurity standards used for?
They are used for analytical method development and validation, impurity identification and quantification, forced-degradation and stability studies, and to support ANDA, DMF and other regulatory submissions under ICH Q3A/Q3B (and ICH M7 for mutagenic impurities).
Can you synthesise a Vancomycin impurity that is not listed?
Yes. Our custom synthesis service can prepare and characterise unlisted impurities, metabolites and labelled analogues from milligram to gram scale. Share the structure or name and required quantity for a quotation.
Request Vancomycin impurity standards
We reply within one business day with price, pack options, lead time and documentation.