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Verapamil EP Impurity I

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COA COO

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Verapamil EP Impurity I

Impurity

CAS Number

1794-55-4

Molecular Formula

C26H36N2O4.ClH

Product format

Neat

Molecular Weight

477.04

USP Description

Verapamil Related Compound B

EP Description

Verapamil impurity I CRS

Storage

+5°C

Shipping

Room Temperature

API Family

Verapamil

Synonyms

Verapamil Hydrochloride Imp. I (EP), Verapamil Imp. I (EP), Verapamil USP Related Compound B, Verapamil USP RC B, (2RS)-2-(3, 4-Dimethoxyphenyl)-2-[2-[[2-(3, 4-dimethoxy-phenyl)ethyl](methyl)amino]ethyl]-3-methyl-butanenitrile Hydrochloride, Verapamil Hydrochloride Imp. I (EP) as Hydrochloride, Verapamil Related Compound B as Hydrochloride, Verapamil Hydrochloride Impurity I as Hydrochloride and Verapamil Impurity I as Hydrochloride

Smiles

Cl.COc1ccc(CCN(C)CCC(C#N)(C(C)C)c2ccc(OC)c(OC)c2)cc1OC

Iupac Name

2-(3, 4-dimethoxyphenyl)-2-[2-[2-(3 and 4-dimethoxyphenyl)ethyl-methylamino]ethyl]-3-methylbutanenitrile;hydrochloride

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
10mg
CE3022.21-10MG

3-4 weeks

25mg
CE3022.21-25MG

3-4 weeks

100mg
CE3022.21-100MG

3-4 weeks

25mg
CD3022.21-25MG

3-5 weeks

100mg
CD3022.21-100MG

3-5 weeks

25mg
CB3022.21-25MG

4-5 weeks

100mg
CB3022.21-100MG

4-5 weeks

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Product Type

Impurity

Our Impurity Characterized Standards portfolio comprises more than 5,000 compounds accompanied by a comprehensive CoA which can be found in 3 product categories that include a set of different analytical techniques for determining Identity and Purity.

API

We have designed a range of primary API standards manufactured according to international regulations that come with the most extensive Certificate of Analysis which includes Identity checks by several techniques.

Excipient

Excipients standards comes with a detailed Certificate of Analysis with Identity, Purity and Assay data. They are also suitable for use with non-compendial analytical methods.

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Synthesis

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