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Vinpocetine EP Impurity A

N° de SZ CAT:SZ-V041002
Número CAS40163-56-2
Mol.F.C22H28N2O3
Peso Molecular368.5
Status de FaturaSynthesis on demand

Nome Químico: Ethyl (12S,13aS,13bS)-13a-ethyl-12-hydroxy- 2,3,5,6,12,13,13a,13b-octahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate (as per EP & USP)

Sinônimo: Ethyl Vincaminate (EP) ; Vinpocetine USP Related Compound A

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CCOC([C@]1(O)N(C2=C3C=CC=C2)C4=C3CCN(CCC5)[C@@]4([H])[C@]5(CC)C1)=O

Vinpocetine EP Impurity A is chemically Ethyl (12S,13aS,13bS)-13a-ethyl-12-hydroxy- 2,3,5,6,12,13,13a,13b-octahydro-1H-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate (as per EP & USP). It is also known as Ethyl Vincaminate (EP) ; Vinpocetine USP Related Compound A. Vinpocetine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Vinpocetine 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 Vinpocetine.

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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