Search Results for " Citalopram "
Citalopram EP Impurity B (Oxalate salt)
| SZ CAT No: | SZ-C039017 |
| CAS No | 1332724-03-4 |
| Mol.F. | C20H21FN2O2 : C2H2O4 |
| Mol.Wt. | 340.4 : 90.0 |
| Inv. Status | In Stock |
| Rel. CAS No | 411221-53-9 (free base) |
Chemical Name: 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate (as per EP) ; 1-(3-Dimethylaminopropyl)-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate (as per USP)
Synonym: Citalopram USP Related Compound B (Oxalate Salt) ; ; 3-Hydroxy Citalopram Oxalate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: OC(C(O)=O)=O.CN(C)CCCC1(C2=CC=C(F)C=C2)C3=CC=C(C#N)C=C3C(O)O1
Citalopram EP Impurity B (Oxalate salt) is chemically 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate (as per EP) ; 1-(3-Dimethylaminopropyl)-1-(4-fluorophenyl)-3-hydroxy-1,3-dihydroisobenzofuran-5-carbonitrile oxalate (as per USP). It is also known as Citalopram USP Related Compound B (Oxalate Salt) ; ; 3-Hydroxy Citalopram Oxalate. Citalopram EP Impurity B (Oxalate salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity B (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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