Diroximel Impurity E - Request Quote
Diroximel Impurity E
| SZ CAT No: | SZ-D079010 |
| CAS No | NA |
| Mol.F. | C11H13NO6 |
| Mol.Wt. | 255.2 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Diroximel Impurity E is chemically 2-(2,5-dioxopyrrolidin-1-yl)ethyl methyl (2Z)-but-2-enedioate. Diroximel Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Diroximel 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 Diroximel Fumarate.
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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Diroximel Impurity E for Method Validation
Diroximel Fumarate Reference Standard
Diroximel Impurity E for ANDA Filing
Diroximel Impurity E for Forced Degradation Studies
Diroximel Impurity E Identification Standards
Diroximel 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.