Worldwide shipping · 120+ destinationsCOA & GHS SDS with every lotMon–Sat, 09:30–18:30 IST
VAQORACHEMICALS
Impurity reference standards

Rosuvastatin impurities & reference standards

Characterised Rosuvastatin impurities, degradation products and related compounds for analytical method development, validation, QC release and regulatory filings.

125reference materials
2isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Rosuvastatin
287714-41-4 · C22H28FN3O6S
View API
Reference Standard
Rosuvastatin Calcium chemical structure
Rosuvastatin Calcium
CAS
147098-20-2
Formula
C44H54CaF2N6O12S2
MW
1001.1 g/mol
VQ-023677
Reference Standard
Rosuvastatin Sodium chemical structure
Rosuvastatin Sodium
CAS
147098-18-8
Formula
C22H27FN3NaO6S
MW
503.5 g/mol
VQ-027899

FAQs — Rosuvastatin impurities

Which Rosuvastatin impurities do you supply?

We list 125 Rosuvastatin-related reference materials, including process impurities, degradation products, stable-isotope-labelled standards and related compounds. Each is supplied with a COA, and characterisation data (HPLC, 1H-NMR, MS, IR) can be provided on request.

What are Rosuvastatin 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 Rosuvastatin 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 Rosuvastatin impurity standards

We reply within one business day with price, pack options, lead time and documentation.

By submitting you agree to our privacy policy. We never share your details.