|Product Name||Ondansetron EP Impurity G|
|Synonyms||Ondansetron BP Impurity G; C-Desmethyl Ondansetron; (3RS)-3-[(1H-Imidazol-1-yl)methyl]-9-Methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one|
Ondansetron EP Impurity G product with CAS: 99614-03-6 is also known as Ondansetron BP Impurity G; C-Desmethyl Ondansetron. This product can be used as working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Ondansetron and its related formulations. Moreover, Ondansetron BP Impurity G is also used in process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Ondansetron developed in our R&D.
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All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, Structure Elucidation etc. will be provided on request (extra charges may apply). Products provide by SynThink are for research and development (R&D) use only.
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