Atorvastatin IMpurity F is a reference standard used primarily for impurity analysis in quality control and research settings. It is the sodium salt form of a complex, multi-functional molecule containing multiple alcohol and amide groups, and is structurally characterized as a salt-like, flexible compound.
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CAS 1371615-56-3
Atorvastatin N-(3,5-Dihydroxy-7-heptanoic Acid)amide
active pharmaceutical ingredient
Difluoro Atorvastatin Calcium Salt
active pharmaceutical ingredient
Calcium;(3R,5R)-7-[2-(4-fluorophenyl)-3-(2,3,4,5,6-pentadeuteriophenyl)-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoate
active pharmaceutical ingredient
N,N-Dimethyl-4-oxo-4-(p-tolyl)butanamide
Reference standard for impurity analysis
({[Benzyl(pyridin-3-ylmethyl)amino]-carbonothioyl}amino)acetic acid
Reference standard for impurity analysis
Topiramate Didesacetal Impurity
Reference standard for impurity analysis
1,6-dibromonaphthalen-2-amine
research chemical intermediate
2,6-dibromonaphthalene
research compound
sodium (3R,5R)-7-[[(3R,5R)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoyl]amino]-3,5-dihydroxyheptanoate
OHFKZDUXUWJNCG-ZNOPIPGTSA-M
CC(C)C1=C(C(=C(N1CC[C@H](C[C@H](CC(=O)NCC[C@H](C[C@H](CC(=O)[O-])O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4.[Na+]