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Pravastatin EP Impurity A

SZ目录编号:SZ-P025002
CAS 号81176-41-2
分子式C23H35O7 : Na
分子量423.5 : 23.0
投资状态Under Synthesis
Rel. CAS No250737-12-3 (free base)

化学名称: Sodium (3R,5R)-3,5-dihydroxy-7-((1S,2S,6R,8S,8aR)-6-hydroxy-2-methyl-8-(((S)-2-methylbutanoyl)oxy)-1,2,6,7,8,8a-hexahydronaphthalen-1-yl)heptanoate

异名: (6R)-Pravastatin Sodium ; Pravastatin USP Related Compound B

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: 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](C[C@@H](O)CC(O[Na])=O)O)=C1

Pravastatin EP Impurity A is chemically Sodium (3R,5R)-3,5-dihydroxy-7-((1S,2S,6R,8S,8aR)-6-hydroxy-2-methyl-8-(((S)-2-methylbutanoyl)oxy)-1,2,6,7,8,8a-hexahydronaphthalen-1-yl)heptanoate. It is also known as (6R)-Pravastatin Sodium ; Pravastatin USP Related Compound B. Pravastatin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Pravastatin 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 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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