Search Results for " Citalopram "
Citalopram EP Impurity G (Dioxalate salt)
| N° de SZ CAT: | SZ-C039044 |
| Número CAS | NA |
| Mol.F. | C25H33FN2O2 : 2(C2H2O4) |
| Peso Molecular | 412.5 : 2(90.0) |
| Status de Fatura | Custom Synthesis |
| Rel. CAS No | 1329745-98-3 (free base) : 2575516-42-4 (HCl salt) : 1329611-41-7 (HBr salt) ; 1440961-12-5 (oxalate salt) |
Nome Químico: 4-(Dimethylamino)-1-[(1RS)-1-[3- (dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2- benzofuran-5-yl]butan-1-one dioxalate (as per EP)
Sinônimo: Citalopram ketone (USP) : 5-Dimethylaminobutyryl Citalopram Oxalate (USP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: O=C(C1=CC=C2C(C3=CC=C(F)C=C3)(CCCN(C)C)OCC2=C1)CCCN(C)C.O=C(C(O)=O)O.O=C(C(O)=O)O
Citalopram EP Impurity G (Dioxalate salt) is chemically 4-(Dimethylamino)-1-[(1RS)-1-[3- (dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2- benzofuran-5-yl]butan-1-one dioxalate (as per EP). It is also known as Citalopram ketone (USP) : 5-Dimethylaminobutyryl Citalopram Oxalate (USP). Citalopram EP Impurity G (Dioxalate salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity G (Dioxalate salt) can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Citalopram.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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