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Citalopram EP Impurity D (HCl salt)

N° de SZ CAT:SZ-C039006
Número CAS97743-99-2
Mol.F.C19H19FN2O : HCl
Peso Molecular310.4 : 36.5
Status de FaturaIn Stock
Rel. CAS No62498-67-3 (free base) ; 1188264-72-3 (HBr 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 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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