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Pravastatin EP Impurity D

N° de SZ CAT:SZ-P025005
Número CAS85956-22-5
Mol.F.C23H34O6
Peso Molecular406.5
Status de FaturaIn Stock

Nome Químico: (1S,3S,7S,8S,8aR)-3-hydroxy-8-(2-((2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (S)-2-methylbutanoate

Sinônimo: Pravastatin Lactone

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O[C@H]1C[C@H](OC([C@@H](C)CC)=O)[C@@]2([H])C(C=C[C@H](C)[C@@H]2CC[C@H]3OC(C[C@H](O)C3)=O)=C1

Pravastatin EP Impurity D is chemically (1S,3S,7S,8S,8aR)-3-hydroxy-8-(2-((2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-7-methyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl (S)-2-methylbutanoate. It is also known as Pravastatin Lactone. Pravastatin EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Pravastatin EP Impurity D 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 Pravastatin.

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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