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Citalopram EP Impurity F; Citalopram Related Compound H

5-Bromo Citalopram Oxalate; Citalopram USP Related Compound H; 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-bromophthalane oxalate;

Citalopram-EP-Impurity-F

Specifications:

CAS No.

: 64169-39-7 (Base); 479065-02-6 (HBr Salt)

Mol F.

: C19H21BrFNO (Base), C21H23BrFNO5 (Oxalate Salt)

Mol W.

: 378.28,468.31(OxalateSalt)

Cat No.

: SA17010

Appearance

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Product Name

: Citalopram EP Impurity F; Citalopram Related Compound H

CAS No.

: 64169-39-7 (Base); 479065-02-6 (HBr Salt)

Mol F.

: C19H21BrFNO (Base), C21H23BrFNO5 (Oxalate Salt)

Mol W.

: 378.28,468.31(OxalateSalt)

Cat No.

: SA17010

Appearance

Synonyms

: 5-Bromo Citalopram Oxalate; Citalopram USP Related Compound H; 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-bromophthalane oxalate;

Related API

: Citalopram

Category

Citalopram EP Impurity F product with CAS: 64169-39-7 (Base); 479065-02-6 (HBr Salt) is also known as Citalopram USP Related Compound H. 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 F is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Citalopram and its related formulations. Moreover, Citalopram USP Related Compound H 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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