Clopidogrel EP Impurity B is a pharmaceutical impurity reference standard. It is the This compound compound, used primarily as a certified reference material in quality control and analytical testing.
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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(±)-clopidogrel bisulfate
pharmaceutical raw material
(2-butyl-1-benzofuran-3-yl)-[4-[2-(diethylamino)ethoxy]-3-iodophenyl]methanone;hydrochloride
pharmaceutical intermediate
O-Desmethyl-O-ethyl Albendazole
pharmaceutical intermediate
5H-Cyclohepta[b]pyridin-5-one, 6-(2,3-difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-, (6R,9R)-
pharmaceutical intermediate
(6R,9S)-6-(2,3-Difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-5H-cyclohepta[b]pyridin-5-one
pharmaceutical intermediate
Clopidogrel Related Compound B
pharmaceutical intermediate
methyl (2S)-2-(2-chlorophenyl)-2-(5,7-dihydro-4H-thieno[2,3-c]pyridin-6-yl)acetate
ZEIGZKQSYIWMTR-HNNXBMFYSA-N
COC(=O)[C@H](C1=CC=CC=C1Cl)N2CCC3=C(C2)SC=C3
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