Clarithromycin Impurity L is a chemical compound used as a reference standard in pharmaceutical manufacturing and quality control for macrolide antibiotics. It is structurally related to clarithromycin and serves as a laboratory tool for impurity profiling and analytical method development.
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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Erythromycin oxime
pharmaceutical raw material
(3R,4S,5S,6R,7R,9R,10E,11S,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-10-hydroxyimino-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecan-2-one
pharmaceutical raw material
PUBCHEM_71314812
pharmaceutical research compound
Clarithromycin
pharmaceutical raw material
(R)-3-Aminopiperidine
pharmaceutical intermediate
3-Methylaminopiperidine dihydrochloride
pharmaceutical intermediate
2-Chloromethyl-3-methyl-4-(2,2,2-trifluoroethoxy)pyridine hydrochloride
pharmaceutical intermediate
Tert-butyl (3R,4R)-3-amino-4-fluoropiperidine-1-carboxylate
pharmaceutical intermediate
6-[4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-12,13-dihydroxy-10-hydroxyimino-4-(5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl)oxy-7-methoxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecan-2-one
MWBJRTBANFUBOX-UHFFFAOYSA-N
CCC1C(C(C(C(=NO)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)N(C)C)O)(C)OC)C)C)O)(C)O
Sourcing Clarithromycin Impurity L?
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