Substance
ID:347956
Names and Identifiers
IUPAC name
sodium (2S,5R,6R)-6-[(2R)-2-amino-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
IUPAC Traditional name
sodium ampicillin(1-)
Synonyms
Ampicillin sodium salt氨苄西林 钠盐氨苄青霉素 钠盐D-(-)-α-Aminobenzylpenicillin sodium salt
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Physical Property
Melting Point
215 °C (dec.)(lit.)
Safety Information
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 Hazard statements
H317-H334
German water hazard class
2
Risk Statements
42/43
RTECS
XH8400000
GHS Signal Word
Danger
GHS Precautionary statements
P261-P280-P342+P311
European Hazard Symbols
Harmful (Xn)Safety Statements
22-36/37-45
MSDS Link
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Storage Temperature
2-8°C
Product Information
Suitability
suitable for cell culture
Empirical Formula (Hill Notation)
C16H18N3NaO4S
Impurities
endotoxin, tested
Product Line
BioXtra
Molecule Details
Application
Used to select for ampicillin resistance in mutated and transformed cells.
Biochem/physiol Actions
A β-lactam antibiotic with an amino group side chain attached to the penicillin structure. Penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli . Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Used to select for ampicillin resistance in mutated and transformed cells.
Biochem/physiol Actions
A β-lactam antibiotic with an amino group side chain attached to the penicillin structure. Penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Bactericidal only to growing Escherichia coli . Mode of resistance: Cleavage of β-lactam ring of ampicillin by β-lactamase. Antimicrobial spectrum: Gram-negative and Gram-positive bacteria.
Protocols & Applications
Antibiotic Selector for application, solubility, solution stability, working concentration, and mode of action information
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data