Kanamycin sulfate
Supplier: RPI
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Danger
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Synonyms:
Kanamycin Monosulphate
, (2R,3S,4S,5R,6R)-2-(Aminomethyl)-6-(((1R,2R,3S,4R,6S)-4,6-diamino-3-(((2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2-hydroxycyclohexyl)oxy)tetrahydro-2H-pyran-3,4,5-triol sulphate
, Kanamycin A
, Kanamycin Monosulfate
, (2R,3S,4S,5R,6R)-2-(Aminomethyl)-6-(((1R,2R,3S,4R,6S)-4,6-diamino-3-(((2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2-hydroxycyclohexyl)oxy)tetrahydro-2H-pyran-3,4,5-triol sulfate
Aminoglycoside antibiotic with a bactericidal action against most gram negative bacteria.
- Soluble in water
Incorporates into sensitive bacterial cells by an active transport process. Binds to the 30S and to some extent the 50S subunits of the bacterial ribosome, inhibiting protein synthesis and generating errors in the transcription of the genetic code. Widely used as a selective agent for the incorporation of the NPT II (APH3') gene in plant tissue.
Caution: Research or further manufacturing use only, not for food or drug use.
Formula:
C₁₈H₃₈N₄O₁₅S MW: 582.6 g/mol Storage Temperature: Ambient |
MDL Number:
MFCD00070253 CAS Number: 25389-94-0 |
Specification Test Results
Appearance | White Powder |
Chromatographic Purity | Pass Test |
Identification | Pass Test |
Loss on Drying | ≤ 1.5 % |
pH (1% Solution) | 6.5 - 8.5 |
Potency | ≥ 750 µg/mg |
Residue on Ignition | ≤ 1.0 % |
Specific Rotation | +116 - +123 ° |
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