Substance
ID:346764
Names and Identifiers
IUPAC Traditional name
kanamycin; sulfuric acid
IUPAC name
(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)oxan-2-yl]oxy}-2-hydroxycyclohexyl]oxy}oxane-3,4,5-triol; sulfuric acid
Synonyms
卡那霉素 A卡那霉素碱 硫酸盐Kanamycin sulfate from Streptomyces kanamyceticus卡那霉素 硫酸酯 来源于卡那霉素链霉菌Kanamycin sulfate saltKanamycin A
Properties
Safety Information
GHS Precautionary statements
P201-P308+P313
Risk Statements
61
Storage Temperature
2-8°C
European Hazard Symbols
Toxic (T)Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
GHS Hazard statements
H360
German water hazard class
2
GHS Pictograms
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS Signal Word
Danger
MSDS Link
RTECS
NZ3225030
Safety Statements
53-45
Product Information
Empirical Formula (Hill Notation)
C18H36N4O11 · H2O4S
Suitability
cell culture tested
Grade
Biotechnology Performance Certified
Impurities
endotoxin, tested
Molecule Details
Application
Use in biotechnology applications to inhibit protein synthesis.
Biochem/physiol Actions
Mode of Action: Binds to 70S ribosomal subunit; inhibits translocation; elicits miscoding. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria, and mycoplasma.
Use in biotechnology applications to inhibit protein synthesis.
Biochem/physiol Actions
Mode of Action: Binds to 70S ribosomal subunit; inhibits translocation; elicits miscoding. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria, and mycoplasma.
Molecular Spectra
No Data Available
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References
No Data Available
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