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

Capivasertib impurities & reference standards

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

20reference materials
COAHPLC · NMR · MS on request
Parent API: Capivasertib
1143532-39-1 · C21H25ClN6O2
View API
Reference Standard
Capivasertib chemical structure
Capivasertib
CAS
1143532-39-1
Formula
C21H25ClN6O2
MW
428.9 g/mol
In stock

FAQs — Capivasertib impurities

Which Capivasertib impurities do you supply?

We list 20 Capivasertib-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 Capivasertib 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 Capivasertib 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 Capivasertib 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.