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Simvastatin EP Impurity A

SZ目录编号:SZ-S008002
CAS 号101314-97-0
分子式C25H39O6 : Na
分子量435.6 : 23.0
投资状态In Stock
Rel. CAT NoSZ-S008014
Rel. CAS No121009-77-6 (free base)

化学名称: (3R,5R)-7-[(1S,2S,6R,8S,8aR)-8-[(2,2-dimethylbutanoyl)oxy]-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid  Sodium (as per EP & USP)

异名: Simvastatin USP Related Compound A ; Simvastatin Sodium ; Simvastatin Acid Sodium Salt ; Simvastatin Hydroxy Acid Sodium Salt (USP) ; Tenivastatin Sodium Salt (EP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

微笑: [H][C@@]1([C@H]([C@H](C=C2)C)CC[C@@H](O)C[C@H](CC([O-])=O)O)C2=C[C@@H](C[C@@H]1OC(C(C)(CC)C)=O)C.[Na+]

Simvastatin EP Impurity A is chemically (3R,5R)-7-[(1S,2S,6R,8S,8aR)-8-[(2,2-dimethylbutanoyl)oxy]-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid  Sodium (as per EP & USP). It is also known as Simvastatin USP Related Compound A ; Simvastatin Sodium ; Simvastatin Acid Sodium Salt ; Simvastatin Hydroxy Acid Sodium Salt (USP) ; Tenivastatin Sodium Salt (EP). Simvastatin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Simvastatin 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 Simvastatin.

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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