3,4-Dimethoxybenzenemethano
Verapamil EP Impurity E is a fully characterized chemical compound used as a reference standard of API Verapamil. The standard offered is compliant with regulatory guidelines. Verapamil EP Impurity E is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 93-03-8
Related products
N-Desmethyl Verapamil-d7 HCl
M.F. C₂₆H₂₉N₂O₄D₇. HCl
M.W. 447.63 36.46
CAT# AR-V01296
CAS# 1216413-74-9
Verapamil EP Impurity A DiHCl
M.F. C₂₅H₃₈N₂O₄. ₂ HCl
M.W. 430.59 2 36.46
CAT# AR-V01304
CAS# 63434-11-7
Verapamil EP Impurity M HCl (Mixture of Diastereomers)
M.F. C₄₂H₅₇N₃O₆. HCl
M.W. 699.94 36.46
CAT# AR-V01313
CAS# 190850-50-1
Verapamil EP Impurity N HCl
M.F. C₃₃H₄₇N₃O₄. HCl
M.W. 549.76 36.46
CAT# AR-V01314
CAS# 2086274-75-9 (free base)
Verapamil EP Impurity O HCl
M.F. C₂₇H₃₈N₂O₄. HCl
M.W. 454.61 36.46
CAT# AR-V01315
CAS# 959011-16-6 (free base)
Verapamil EP Impurity P (Mixture of Diastereomers)
M.F. C₂₉H₃₈N₂O₄
M.W. 478.63
CAT# AR-V01316
CAS# NA
Verapamil Impurity 1 hydrobromide
M.F. C₁₂H₁₉NO₂. HBr
M.W. 209.29 80.91
CAT# AR-V01317
CAS# 1551304-28-9 (free base)
