CAS No.: 217636-48-1 - Fenofibrate EP Impurity G

Fenofibrate EP Impurity G

CAS No. : 217636-48-1
Synonyms : Fenofibrate USP Related Compound C; 1-Methylethyl 2-[[2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoyl]oxy]-2-methylpropanoate; Fenofibric Acid 1,1-Dimethyl-2-(1-methylethoxy)-2-oxoethyl Ester; 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methylpropanoic Acid 1,1-Dimethyl-2-(1-methylethoxy)-2-oxoethyl Ester
Catalog No. : SA27207

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Product Description

Product NameFenofibrate EP Impurity G
CAS Number217636-48-1
SynonymsFenofibrate USP Related Compound C; 1-Methylethyl 2-[[2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoyl]oxy]-2-methylpropanoate; Fenofibric Acid 1,1-Dimethyl-2-(1-methylethoxy)-2-oxoethyl Ester; 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methylpropanoic Acid 1,1-Dimethyl-2-(1-methylethoxy)-2-oxoethyl Ester
Catalog NumberSA27207
Molecular FormulaC24H27ClO6
Molecular Weight446.92
Related APIFenofibrate
CategoryImpurities

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Fenofibrate EP Impurity G product with CAS number 217636-48-1 and catalog number SA27207 is related to Fenofibrate. This product is used for Abbreviated New Drug Application (ANDA) filing to FDA as well as for Quality Control (QC), toxicity studies and other analytical studies during commercial production of Fenofibrate. Fenofibrate is belomging tothe fibrate class which is mainly used to to reduce cholesterol levels in people at risk of cardiovascular disease. It reduces both low-density lipoprotein (LDL) and very low density lipoprotein (VLDL) levels, as well as increasing high-density lipoprotein (HDL) levels and reducing triglyceride levels. All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). This product is for research and development (R&D) use only., product with CAS number and catalog number is related to . This product is used for Abbreviated New Drug Application (ANDA) filing to FDA as well as for Quality Control (QC), toxicity studies and other analytical studies during commercial production of . All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). This product is for research and development (R&D) use only.

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