Impurity reference standards
Simvastatin impurities & reference standards
Characterised Simvastatin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.
25reference materials
COAHPLC · NMR · MS on request
Des(2-methylbutyryl) Lovastatin Hydroxy Acid Sodium Salt
- CAS
- 132294-94-1
- Formula
- C19H29NaO5
- MW
- 360.4 g/mol
VQ-035075
FAQs — Simvastatin impurities
Which Simvastatin impurities do you supply?
We list 25 Simvastatin-related reference materials, including process impurities, degradation products and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.
What are Simvastatin 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 Simvastatin 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 Simvastatin impurity standards
We reply within one business day with price, pack options, lead time and documentation.