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Vamorolone Impurity 13

N° de SZ CAT:SZ-V054010
Número CAS
489459-63-4
Mol.F.
C22H30O4
Peso Molecular
358.5
Status de Fatura
Synthesis on demand

Nome Químico: (8S,10S,13S,14S,16R,17R)-17-((S)-1,2-Dihydroxyethyl)-17-hydroxy-10,13,16-trimethyl-6,7,8,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-3-one

Shipping Temperature:

HSN Code: 38229010

Country of Origin: India

Sorrisos: C[C@@]1([C@@]2(O)[C@@H](O)CO)[C@](C[C@H]2C)([H])[C@@](CCC3=CC4=O)([H])C([C@]3(C=C4)C)=CC1

Vamorolone Impurity 13 is chemically (8S,10S,13S,14S,16R,17R)-17-((S)-1,2-Dihydroxyethyl)-17-hydroxy-10,13,16-trimethyl-6,7,8,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-3-one. Vamorolone Impurity 13 is supplied with detailed characterization data compliant with regulatory guideline. Vamorolone Impurity 13 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 Vamorolone.

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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