Buspirone EP Impurity I
|CAS No.||: NA|
|Mol F.||: C21H30ClN5O2|
|Mol W.||: 419.95|
|Cat No.||: SA25808|
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|Product Name||Buspirone EP Impurity I|
|Synonyms||5-Chloro Buspirone (USP)|
Buspirone EP Impurity I product with CAS: NA is related to Buspirone. It is also known with other names such as 5-Chloro Buspirone (USP); 8-[4-[4-(5-Chloropyrimidin-2-yl)piperazin-1-yl]butyl]-8-azaspiro[4.5]decane-7,9-dione. Buspirone EP Impurity I used for Abbreviated New Drug Application (ANDA) & DMF filing to FDA, toxicity study of respective drug formulation, Quality Control (QC), and analytical studies during commercial production of Buspirone.
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This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.
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