This compound is a specified impurity of the aminoglycoside antibiotic amikacin, designated as Amikacin EP Impurity G according to the European Pharmacopoeia. It serves as a reference standard for analytical testing and quality control in pharmaceutical manufacturing.
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 50896-99-6
(2S)-4-amino-N-[(1S,2R,3R,4S,5R)-5-amino-4-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxycyclohexyl]-2-hydroxybutanamide
pharmaceutical raw material
(−)-ephedrine hemihydrate
pharmaceutical raw material
Mizoribine
pharmaceutical raw material
Diatrizoic acid dihydrate
pharmaceutical raw material
Procaine hydrochloride
pharmaceutical raw material
Amikacin hydrate
pharmaceutical raw material
Amikacin sulfate salt
pharmaceutical raw material
Amikacin
antibiotic active pharmaceutical ingredient
(2R)-4-amino-N-[(1R,2S,3S,4R,5S)-5-amino-2-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxycyclohexyl]-2-hydroxybutanamide
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