Fulvestrant EP Impurity D is a chemical reference standard used in the quality control and analytical testing of the pharmaceutical ingredient fulvestrant. It is a related substance that may appear during the synthesis or storage of fulvestrant and is employed to ensure the purity and consistency of the drug substance.
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 2483797-59-5
(7a,17b)-7-(9-Bromononyl)estra-1,3,5(10)-triene-3,17-diol
pharmaceutical intermediate
(7a,17b)-7-[9-[(4,4,5,5,5-Pentafluoropentyl)thio]nonyl]-estra-1,3,5(10)-triene-3,17-diol
pharmaceutical intermediate
O-Chlorobutylabiraterone
Research compound
2-chloro-N-(2-(2-chlorobenzoyl)-4-nitrophenyl)benzamide
research compound
6-Chloro-3-iodo-2-methylpyridine
research reagent
Triethyl orthobutyrate
Chemical intermediate
(8R,9S,13S,14S,17S)-7-[9-[(8R,9S,13S,14S,17S)-3,17-dihydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-7-yl]nonyl]-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
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