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 |
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Description
| Product Name | Citalopram EP Impurity F; Citalopram Related Compound H |
| Synonyms | Citalopram USP Related Compound H
5-Bromo Citalopram Oxalate 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-bromophthalane oxalate |
| Related API | Citalopram |
| Category | Impurities |
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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