Citalopram EP Impurity C; Citalopram Related Compound C
| CAS No. | : 1440961-11-4; 372941-54-3 (free base) |
| Mol F. | : C20H19FN2O2 (base), C22H21FN2O6 (oxalate salt) |
| Mol W. | : 338.38,428.41(oxalatesalt) |
| Cat No. | : SA17007 |
- Description
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Description
| Product Name | Citalopram EP Impurity C; Citalopram Related Compound C |
| Synonyms | Citalopram USP Related Compound C
3-Oxo Citalopram Oxalate EsCitalopram EP Impurity C 3-[3-(Dimethylamino)-1-propyl](4-fluorophenyl)-6-cyano-1(3H)-isobenzofuranone oxalate |
| Related API | Citalopram |
| Category | Impurities |
Citalopram EP Impurity C product with CAS: 1440961-11-4; 372941-54-3 (free base) is also known as Citalopram USP Related Compound C. 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 C is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Citalopram and its related formulations. Moreover, Citalopram USP Related Compound C 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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