Clindamycin Phosphate for System Suitability EPCRS – Inhouse Standard - Request Quote

Clindamycin Phosphate for System Suitability EPCRS – Inhouse Standard is chemically Contain Clindamycin Phosphate (Cas No.: 24729-96-2 , Cat No.: SZ-C076001) , Clindamycin EP Impurity B (Cas No.: 18323-43-8 , Cat No.: SZ-C076048), Clindamycin EP Impurity E (Cas No.: 1440605-51-5 , Cat No.: SZ-C076078), Clindamycin EP Impurity F (Cas No.: 1440605-46-8 , Cat No.: SZ-C076077), Clindamycin Phosphate EP Impurity G (Cas No.: NA , Cat No.: SZ-C076008), Clindamycin Phosphate EP Impurity I (Cas No.: NA , Cat No.: SZ-C076010), Clindamycin Phosphate EP Impurity J (Cas No.: 1309349-64-1 , Cat No.: SZ-C076011), Clindamycin EP Impurity F (Cas No.: 1440605-46-8 , Cat No.: SZ-C076077), Clindamycin Phosphate EP Impurity K (Cas No.: NA , Cat No.: SZ-C076012), Clindamycin Phosphate EP Impurity Lx (Cas No.: 620181-05-7 , Cat No.: SZ-C076013),. Clindamycin Phosphate for System Suitability EPCRS – Inhouse Standard is supplied with detailed characterization data compliant with regulatory guideline. Clindamycin Phosphate for System Suitability EPCRS – Inhouse Standard 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 Clindamycin.

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.