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Vamorolone Impurity 16

N° de SZ CAT:SZ-V054012
Número CAS
34542-56-8
Mol.F.
C24H32O5
Peso Molecular
400.5
Status de Fatura
Synthesis on demand

Nome Químico: 2-((8S,10S,13S,14S,16R,17R)-17-Hydroxy-10,13,16-trimethyl-3-oxo-2,3,6,7,8,10,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate

Shipping Temperature:

HSN Code: 38229010

Country of Origin: India

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

Vamorolone Impurity 16 is chemically 2-((8S,10S,13S,14S,16R,17R)-17-Hydroxy-10,13,16-trimethyl-3-oxo-2,3,6,7,8,10,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate. Vamorolone Impurity 16 is supplied with detailed characterization data compliant with regulatory guideline. Vamorolone Impurity 16 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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