Escitalopram EP Impurity D
|CAS No.||: 144025-14-9 (HCl salt); 1188264-72-3 (HBr salt)|
|Mol F.||: C19H20ClFN2O|
|Mol W.||: 346.83|
|Cat No.||: SA21204|
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|Product Name||Escitalopram EP Impurity D|
|Synonyms||Citalopram EP Impurity D|
Citalopram USP Related Compound D
N-Desmethyl Citalopram HCl
1-(4′-Fluorophenyl)-1-(3-(methylamino)propyl)-1,3-dihydro isobenzo furan-5-carbonitrile hydrochloride
Escitalopram EP Impurity D product with CAS: 144025-14-9 (HCl salt); 1188264-72-3 (HBr salt) is also known as Citalopram EP Impurity D; Citalopram USP Related Compound D. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Escitalopram and its related formulations. Moreover, Citalopram EP Impurity D is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Escitalopram developed in our R&D.
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This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.
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