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 |
- Description
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Description
| Product Name | Citalopram EP Impurity E |
| Synonyms | Citalopram USP Related Compound G
Citalopram 5-Chloro Analog HBr 1-(4′-Fluorophenyl)-1-(3-dimethylaminopropyl)-5-chlorophthalane hydrobromide |
| Related API | Citalopram |
| Category | Impurities |
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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