Simvastatin for system suitability EPCRS-Inhouse standard - Solicitar cotización

Simvastatin for system suitability EPCRS-Inhouse standard is chemically Contain Simvastatin (Cas No : 79902-63-9 , Cat No ; SZ-S008001 , Simvastatin EP Impurity A (Cas No : 101314-97-0 , Cat No ; SZ-S008002 , Simvastatin EP Impurity B (Cas No ;145576-25-6 , Cat No ; SZ-S008003, Simvastatin EP Impurity C (Cas No ; 210980-68-0 , Cat No ; SZ-S008004 ,Simvastatin EP Impurity D (Cas No; 476305-24-5 , Cat No ; SZ-S008005 ,Simvastatin EP Impurity E (Cas No ; 75330-75-5 Cat No ; SZ-S008006 , Simvastatin EP Impurity F ( Cas No ; 79952-44-6 Cat No ; SZ-S008007 , Simvastatin EP Impurity G (Cas No ; 1449248-72-9, Cat No; SZ-S008008, Simvastatin EP Impurity J (Cas No ; 864357-88-0 Cat No ; SZ-S008024. Simvastatin for system suitability EPCRS-Inhouse standard is supplied with detailed characterization data compliant with regulatory guideline. Simvastatin 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 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.