Citalopram EP Impurity E (HBr salt) | CAS 1332724-08-9 - Request Quote
Citalopram EP Impurity E (HBr salt)
| SZ CAT No: | SZ-C039007 |
| CAS No | 1332724-08-9 |
| Mol.F. | C19H21ClFNO : HBr |
| Mol.Wt. | 333.8 : 80.0 |
| Inv. Status | Under Synthesis |
| Rel. CAS No | 64169-45-5 (free base) ; 1329612-81-8 (oxalate salt) |
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Usage Note:
Citalopram EP Impurity E (HBr salt) is chemically 3-[(1RS)-5-chloro-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-1-yl]-N,N-dimethylpropan-1-amine hydrobromide (as per EP). It is also known as Citalopram USP Related Compound G ; Citalopram 5-Chloro Analog HBr ; . Citalopram EP Impurity E (HBr salt) is supplied with detailed characterization data compliant with regulatory guideline. Citalopram EP Impurity E (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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Citalopram EP Impurity E (HBr salt) for Method Validation
Citalopram Reference Standard
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Citalopram EP Impurity E (HBr salt) for Forced Degradation Studies
Citalopram EP Impurity E (HBr salt) Identification Standards
Citalopram EP Impurity E (HBr salt) for DMF Filing
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