Atomoxetine EP Impurity D | CAS 1643684-05-2 - Request Quote
Atomoxetine EP Impurity D
| SZ CAT No: | SZ-A036005 |
| CAS No | 1643684-05-2 |
| Mol.F. | C17H21NO : HCl |
| Mol.Wt. | 255.4 : 36.5 |
| Inv. Status | In Stock |
| Rel. CAS No | 1643684-02-9 (free base) |
Chemical Name :
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Usage Note:
Atomoxetine EP Impurity D is chemically (3R)-N-Methyl-3-(3-methylphenoxy)-3-phenylpropan-1-amine hydrochloride (as per EP) ; (R)-N-Methyl-3-phenyl-3-(3-tolyloxy)propan-1-amine hydrochloride (as per USP). It is also known as Atomoxetine USP Related Compound B ; m-Methyl Atomoxetine HCl. Atomoxetine EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Atomoxetine EP Impurity D 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 Atomoxetine .
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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Atomoxetine EP Impurity D for Method Validation
Atomoxetine Reference Standard
Atomoxetine EP Impurity D for ANDA Filing
Atomoxetine EP Impurity D for Forced Degradation Studies
Atomoxetine EP Impurity D Identification Standards
Atomoxetine EP Impurity D for DMF Filing
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