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VAQORACHEMICALS
Impurity reference standards

Verapamil impurities & reference standards

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

55reference materials
4isotope-labelled
COAHPLC · NMR · MS on request
Parent API: Verapamil Hydrochloride
52-53-9 · C27H38N2O4
View API
Reference Standard
Norverapamil D7 chemical structure
Norverapamil D7
CAS
263175-44-6
Formula
C26H36N2O4
MW
447.6 g/mol
VQ-044788
Reference Standard
Verapamil chemical structure
Verapamil
CAS
52-53-9
Formula
C27H38N2O4
MW
454.6 g/mol
VQ-007843
Reference Standard
Verapamil N-Oxide chemical structure
Verapamil N-Oxide
CAS
123861-30-3
Formula
C27H38N2O5
MW
470.6 g/mol
In stock

FAQs — Verapamil impurities

Which Verapamil impurities do you supply?

We list 55 Verapamil-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 Verapamil 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 Verapamil 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 Verapamil impurity standards

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

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