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Escitalopram Oxalate EP Impurity E as Hydrobromide

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COA COO

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Escitalopram Oxalate EP Impurity E as Hydrobromide

Impurity

CAS Number

103146-26-5

Molecular Formula

C20H23FN2O2.BrH

Product format

Neat

Molecular Weight

423.32

Storage

+5°C

Shipping

Room Temperature

API Family

Escitalopram Oxalate and Citalopram Hydrobromide

Synonyms

4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)-Benzonitrile hydrobromide (1:1), Citadiol Hydrobromide, (4RS)-4-[4-Cyano-2-(hydroxymethyl)phenyl]-4-(4-fluorophenyl)-4-hydroxy-N, N-dimethylbutan-1-aminium Hydrobromide, Escitalopram Oxalate Impurity E as Hydrobromide and Escitalopram Impurity E as Hydrobromide

Smiles

Br.CN(C)CCCC(O)(c1ccc(F)cc1)c2ccc(cc2CO)C#N

Iupac Name

4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl]-3-(hydroxymethyl)benzonitrile;hydrobromide

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COA COO

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Available products

Pack Size SKU
Category Expected Delivery Price Quantity
25mg
CE4483.46-25MG

In Stock(Pending QC - 1-2 weeks)

100mg
CE4483.46-100MG

In Stock(Pending QC - 1-2 weeks)

250mg
CE4483.46-250MG

In Stock(Pending QC - 1-2 weeks)

25mg
CD4483.46-25MG

In Stock(Pending QC - 2-3 weeks)

100mg
CD4483.46-4X25MG

In Stock(Pending QC - 2-3 weeks)

25mg
CB4483.46-25MG

In Stock(Pending QC - 2-3 weeks)

100mg
CB4483.46-4X25MG

In Stock(Pending QC - 2-3 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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