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Dihydroergotamine EP Impurity A | CAS 113-15-5 - Request Quote

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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

Chemical Name :

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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 DMF Filing

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SynZeal will update these details as per new developments or findings in product specifications without further notice.

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