Estradiol Valerate EP Impurity I - Solicitar cotización

Estradiol Valerate EP Impurity I is chemically (1S,3aS,3bR,10aR,10bS,13S,13aS,15aS,18bS,20aS)-13a,17,17,20a-tetramethyl-2,3,3a,3b,4,5,9,10,10a,10b,11,12,13,13a,14,15,15a,17,18b,19,20,20a-docosahydro-1H-bis(cyclopenta[5,6]naphtho)[1,2-b:2ʹ,1ʹ-i]xanthene-1,13-diyl dipentanoate (as per EP). Estradiol Valerate EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Estradiol Valerate EP Impurity I 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 Estradiol Valerate.

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.