Search Results for " Citalopram "
Citalopram EP Impurity D (HBr salt)
| N° de SZ CAT: | SZ-C039019 |
| Número CAS | 1188264-72-3 |
| Mol.F. | C19H19FN2O : HBr |
| Peso Molecular | 310.4 : 80.9 |
| Status de Fatura | In Stock |
| Rel. CAS No | 62498-67-3 (free base) ; 97743-99-2 (HCl salt) |
Nome Químico: (1RS)-1-(4-fluorophenyl)-1-[3-(methylamino)propyl]-1,3-dihydroisobenzofuran-5-carbonitrile hydrochloride (as per EP) ; 1-(4-Fluorophenyl)-1-(3-methylaminopropyl)-1,3-dihydroisobenzofuran-5-carbonitrile hydrobromide (as per USP)
Sinônimo: Citalopram USP Related Compound D ; N-Desmethyl Citalopram HBr
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: N#CC1=CC2=C(C(CCCNC)(C3=CC=C(F)C=C3)OC2)C=C1.Br
Citalopram EP Impurity D (HBr salt) is chemically (1RS)-1-(4-fluorophenyl)-1-[3-(methylamino)propyl]-1,3-dihydroisobenzofuran-5-carbonitrile hydrochloride (as per EP) ; 1-(4-Fluorophenyl)-1-(3-methylaminopropyl)-1,3-dihydroisobenzofuran-5-carbonitrile hydrobromide (as per USP). It is also known as Citalopram USP Related Compound D ; N-Desmethyl Citalopram HBr. Citalopram EP Impurity D (HBr salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity D (HBr 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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