Search Results for " Citalopram "
Citalopram EP Impurity E (Oxalate salt)
| N° de SZ CAT: | SZ-C039041 |
| Número CAS | 1329612-81-8 |
| Mol.F. | C19H21ClFNO : C2H2O4 |
| Peso Molecular | 333.8 : 90.0 |
| Status de Fatura | In Stock |
| Rel. CAS No | 64169-45-5 (free base) ; 1332724-08-9 (HBr salt) |
Nome Químico: 3-[(1RS)-5-chloro-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-1-yl]-N,N-dimethylpropan-1-amine oxalate (as per EP)
Sinônimo: Citalopram USP Related Compound G ; Citalopram 5-Chloro Analog oxalate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: CN(C)CCCC1(C2=CC=C(F)C=C2)C(C=CC(Cl)=C3)=C3CO1.OC(C(O)=O)=O
Citalopram EP Impurity E (Oxalate salt) is chemically 3-[(1RS)-5-chloro-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-1-yl]-N,N-dimethylpropan-1-amine oxalate (as per EP). It is also known as Citalopram USP Related Compound G ; Citalopram 5-Chloro Analog oxalate. Citalopram EP Impurity E (Oxalate salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity E (Oxalate 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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