This compound is an impurity reference standard of midazolam, specifically designated as Midazolam EP Impurity G. It is used in pharmaceutical quality control and analytical testing to ensure the purity and stability of midazolam active pharmaceutical ingredients.
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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Midazolam hydrochloride
pharmaceutical raw material
Midazolam
pharmaceutical raw material
8-Chloro-6-(2-fluorophenyl)-1-methyl-5-oxo-4H-5λ⁵-imidazo[1,5-a][1,4]benzodiazepine
pharmaceutical raw material
Ethyl 8-chloro-6-(2-fluorophenyl)-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate
pharmaceutical raw material
Midazolam 6H-
pharmaceutical raw material
Somatostatin, tyr(11)-
pharmaceutical raw material
1-hydroxymidazolam
pharmaceutical raw material
8-Chloro-6-(o-fluorophenyl)-1-methyl-4H-imidazo(1,5-a)(1,4)benzodiazepine-3-carboxylic acid
pharmaceutical intermediate
8-chloro-1-methyl-6-phenyl-4H-imidazo[1,5-a][1,4]benzodiazepine
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CC1=NC=C2N1C3=C(C=C(C=C3)Cl)C(=NC2)C4=CC=CC=C4
Sourcing Midazolam EP Impurity G?
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