Dihydroergotamine EP Impurity A | CAS 113-15-5 - Request Quote
Dihydroergotamine EP Impurity A
| SZ CAT No: | SZ-D117002 |
| CAS No | 113-15-5 |
| Mol.F. | C33H35N5O5 |
| Mol.Wt. | 581.7 |
| Inv. Status | Synthesis on demand |
| Shipping Condition | Room Temperature |
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Usage Note:
Dihydroergotamine EP Impurity A is chemically (6aR,9R)-N-[(2R,5S,10aS,10bS)-5-Benzyl-10b-hydroxy-2-methyl-3,6-dioxooctahydro-8H-oxazolo[3,2-a]pyrrolo[2,1-c]pyrazin-2-yl]-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide (as per EP). It is also known as Ergotamine (EP). Dihydroergotamine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Dihydroergotamine EP Impurity A 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 Dihydroergotamine.
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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Dihydroergotamine EP Impurity A for Method Validation
Dihydroergotamine Reference Standard
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Dihydroergotamine EP Impurity A for Forced Degradation Studies
Dihydroergotamine EP Impurity A Identification Standards
Dihydroergotamine EP Impurity A for DMF Filing
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