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Citalopram EP Impurity E

Citalopram 5-Chloro Analog HBr; Citalopram USP Related Compound G; 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-chlorophthalane hydrobromide;

Citalopram-EP-Impurity-E

Specifications:

CAS No.

: 1332724-08-9 (HBr); 64169-45-5 (Base); 64169-46-6 (Oxalate)

Mol F.

: C19H22BrClFNO

Mol W.

: 414.74

Cat No.

: SA17009

Appearance

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Product Name

: Citalopram EP Impurity E

CAS No.

: 1332724-08-9 (HBr); 64169-45-5 (Base); 64169-46-6 (Oxalate)

Mol F.

: C19H22BrClFNO

Mol W.

: 414.74

Cat No.

: SA17009

Appearance

Synonyms

: Citalopram 5-Chloro Analog HBr; Citalopram USP Related Compound G; 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-chlorophthalane hydrobromide;

Related API

: Citalopram

Category

Citalopram EP Impurity E product with CAS: 1332724-08-9 (HBr); 64169-45-5 (Base); 64169-46-6 (Oxalate) is also known as Citalopram USP Related Compound G. This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Citalopram EP Impurity E is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Citalopram and its related formulations. Moreover, Citalopram USP Related Compound G is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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