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  6. Ampicillin Trihydrate, MP Biomedicals™

Ampicillin Trihydrate, MP Biomedicals™

Catalog Number p-7083049
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Quantity:
5 g
25 g
This item is not returnable. View return policy
7177-48-2
C16H25N3O7S
403.45
RXDALBZNGVATNY-CWLIKTDRSA-N
Aminobenzylpenicillin trihydrate, alpha-Aminobenzylpenicillin trihydrate ;D[-]-α-Aminobenzylpenicillin, 6-[D(-)-α-Aminophenylacetamido]penicillanic acid
23565
CHEBI:31209
(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;trihydrate
CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.O.O.O
This item is not returnable. View return policy
7177-48-2
C16H25N3O7S
403.45
RXDALBZNGVATNY-CWLIKTDRSA-N
Aminobenzylpenicillin trihydrate, alpha-Aminobenzylpenicillin trihydrate ;D[-]-α-Aminobenzylpenicillin, 6-[D(-)-α-Aminophenylacetamido]penicillanic acid
23565
CHEBI:31209
(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;trihydrate
CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)O)C.O.O.O

Description

Active as a broad-spectrum antibiotic. Ampicillin Trihydrate, MP Biomedicals is a semi-synthetic derivative of penicillin that is commonly used to select for ampicillin resistance in mutated and transformed cells. It is also used for enhancing luminol che

Ampicillin trihydrate is a β-lactam antibiotic with an amino group side chain attached to the penicillin structure. It is a penicillin derivative that inhibits bacterial cell-wall synthesis (peptidoglycan cross-linking) by inactivating transpeptidases on the inner surface of the bacterial cell membrane.

  • Inactivated by beta-lactamases; therefore, a beta-lactamase inhibitor should be considered when using ampicillin
  • Antimicrobial spectrum: gram-negative and gram-positive bacteria.
    • 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
  • Bactericidal only to growing E. coli. Inhibits cell wall synthesis via cleavage of β-lactam ring of ampicillin by β-lactamase
Physical Form Powder
Melting Point 198°C to 200°C (literature)
Solubility Information Soluble in 1M Ammonium Hydroxide (50mg/mL), dilute acids (50mg/mL 1M HCl) or bases; slightly soluble in water (10mg/mL); practically insoluble in alcohol, chloroform, ether and fixed oils.
Formula Weight 403.46
Concentration Working Concentration: 100mg/liter for both gram positive and gram negative bacteria. It is typically stable in media at 37°C for approximately 3 days.
Quantity 5 g
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