Metoclopramide EP Impurity E | CAS 100-36-7 - Request Quote
Metoclopramide EP Impurity E
| SZ CAT No: | SZ-M015006 |
| CAS No | 100-36-7 |
| Mol.F. | C6H16N2 |
| Mol.Wt. | 116.2 |
| Inv. Status | In Stock |
| Shipping Condition | Room Temperature |
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Metoclopramide EP Impurity E is chemically N1,N1-diethylethane-1,2-diamine. It is also known as Metoclopramide BP Impurity E ; 2-Diethylaminoethylamine. Metoclopramide EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Metoclopramide EP Impurity E 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 Metoclopramide.
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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Metoclopramide EP Impurity E for Method Validation
Metoclopramide Reference Standard
Metoclopramide EP Impurity E for ANDA Filing
Metoclopramide EP Impurity E for Forced Degradation Studies
Metoclopramide EP Impurity E Identification Standards
Metoclopramide EP Impurity E for DMF Filing
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SynZeal will update these details as per new developments or findings in product specifications without further notice.


