(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-cyclopenta[5,6]naphtho[1,2-b]cyclopenta[5,6]naphtho[2,1-i]xanthene-1,13-diyl dipentanoate
Estradiol Valerate EP Impurity I is a fully characterized chemical compound used as a reference standard of API Estradiol. The standard offered is compliant with regulatory guidelines. Estradiol Valerate EP Impurity I is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS -
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