Ampicillin sodium salt
Supplier: MP Biomedicals
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Danger
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Synonyms:
D(-)-α-Aminobenzylpenicillin Sodium Salt
Ampicillin is a semi-synthetic derivative of penicillin, active as a broad-spectrum antibiotic.
It is inactivated by beta-lactamases and for this reason a beta-lactamase inhibitor should be considered when using ampicillin. Against gram-positive bacteria, ampicillin has a similar mode of action as benzylpenicillin; against gram-negative bacteria, it has a similar mode of action as chloramphenicol and tetracyclines. In E. coli it inhibits cell wall synthesis.
Used to select for ampicillin resistance in mutated and transformed cells.
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.
Soluble in water (50 mg/ml); soluble in 1 M ammonium hydroxide, dilute acids or bases; practically insoluble in alcohol, chloroform, ether and fixed oils.
Formula:
C₁₆H₁₈N₃NaO₄S MW: 371,39 g/mol Storage Temperature: Refrigerator |
MDL Number:
MFCD00064313 CAS Number: 69-52-3 |
Specification Test Results
Synonyms | D(-)-α-Aminobenzylpenicillin sodium salt |
Storage | Store at +4 °C |
Loss on Drying |
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pH | 8 - 10 (1% aq soln) |
pka | pKa = 2,5 (-COOH) pKa = 7,3 (-NH2) at 25 °C |
Potency |
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