Search Results for " Citalopram "
Citalopram EP Impurity D (HCl salt)
| N° de SZ CAT: | SZ-C039006 |
| Número CAS | 97743-99-2 |
| Mol.F. | C19H19FN2O : HCl |
| Peso Molecular | 310.4 : 36.5 |
| Status de Fatura | In Stock |
| Rel. CAS No | 62498-67-3 (free base) ; 1188264-72-3 (HBr salt) |
| Shipping Condition | Ambient Temperature |
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 hydrochloride (as per USP)
Sinônimo: Citalopram USP Related Compound D ; N-Desmethyl Citalopram HCl
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.Cl
Citalopram EP Impurity D (HCl 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 hydrochloride (as per USP). It is also known as Citalopram USP Related Compound D ; N-Desmethyl Citalopram HCl. Citalopram EP Impurity D (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity D (HCl 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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