Synonym:
D-(−)-α-Aminobenzylpenicillin,
Ampicillin trihydrate
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CAS Number 7177-48-2
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Empirical Formula (Hill Notation) C16H19N3O4S · 3H2O
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Molecular Weight 403.45
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Beilstein Registry Number 5399534
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EC Number 200-709-7
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MDL number MFCD00072036
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PubChem Substance ID 329823367
Properties:
Related Categories |
Additional Standards,
Analytical Standards,
Analytical/Chromatography,
Chromatography,
Pharmaceutical Secondary Standards,
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grade
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certified reference material
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pharmaceutical secondary standard
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InChI Key
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RXDALBZNGVATNY-CWLIKTDRSA-N
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form
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neat
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mp
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198-200 °C (dec.)(lit.)
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format
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neat
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pharmacopeia traceability
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traceable to BP 21/785
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traceable to PhEur A1000000/A1100000
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traceable to USP 1033000/1033407
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Description:
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.
General description
Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Footnote
To see an example of a Certificate of Analysis for this material enter LRAA1900 in the slot below. This is an example certificate only and may not be the lot that you receive.
Safety:
Symbol


GHS07, GHS08
Hazard statements
H315-H317-H319-H334-H335
Precautionary statements
P261-P280-P305 + P351 + P338-P342 + P311
RIDADR
NONH for all modes of transport