4-(4-(pyrimidin-2-yl)piperazin-1-yl)butyl 2-(1-(2-oxo-2-((4-(4-(pyrimidin-2-yl)piperazin-1-yl)butyl)amino)ethyl)cyclopentyl)acetate; Buspirone Open Ring Dimer Impurity (USP); 1-[2-oxo-2-[[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]amino]ethyl]-4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl ester Cyclopentaneacetic acid
Buspirone EP Impurity F is a fully characterized chemical compound used as a reference standard of API Buspirone. The standard offered is compliant with regulatory guidelines. Buspirone EP Impurity F 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 - 2512210-24-9
Related products
N-Nitroso Buspirone impurity ; 2-(4-Nitrosopiperazin-1-yl)pyrimidine
M.F.
M.W. 193.21
CAT# AR-B05684
CAS# 872826-80-7
Buspirone Impurity 1 (Lactone of 6-Hydroxy Buspirone)
M.F.
M.W. 401.51
CAT# AR-B02303
CAS# 125498-83-1
