Nilotinib Impurity 12 is a fully characterized chemical compound used as a reference standard of API Lumacaftor. The standard offered is compliant with regulatory guidelines. Nilotinib Impurity 12 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 - NA
Related products
3-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline

M.F. C₁₀H₈F₃N₃
M.W. 227.19
CAT# AR-N01540
CAS# 943320-48-7
3-(5-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline

M.F. C₁₁H₁₀F₃N₃
M.W. 241.22
CAT# AR-N01542
CAS# 641571-16-6
Nilotinib N-Oxide (Imidazole N-Oxide)

M.F. C₂₈H₂₂F₃N₇O₂
M.W. 545.53
CAT# AR-N01553
CAS# 2139382-75-3
3-(Dimethylamino)-1-(pyridin-2-yl)prop-2-en-1-one

M.F. C₁₀H₁₂N₂O
M.W. 176.2
CAT# AR-N08096
CAS# 66521-54-8