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Ampicillin, sodium salt, 50 mg

Ampicillin, sodium salt, 50 mg

$38.10

Key features and details

Ampicillin Sodium Salt

SKU: 0219419950

Synonyms
D[-]-α-Aminobenzylpenicillin; 6-[D(-)-α-Aminophenylacetamido]penicillanic acid; D-(−)-α-Aminobenzylpenicillin sodium salt; Aminobenzylpenicillin sodium salt
CAS Number:
69-52-3
Molecular Formula:
C16H18N3NaO4S
Molecular Weight:
371.387 g/mol
Beilstein Registry Number:
4119211
EC Number:
200-708-1
MDL Number:
MFCD00064313
Packaging size:
50 mg
Product Description

Ampicillin Sodium Salt

Application Notes

Ampicillin sodium salt is used to select for ampicillin resistance in mutated and transformed cells. It is also described for the use of inhancing luminol chemiluminescence.

Usage Statement

Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Key Applications

Antibiotic

Documents

Datasheet

Datasheet
Specifications
SKU 0219419950
Alternate Names D[-]-α-Aminobenzylpenicillin; 6-[D(-)-α-Aminophenylacetamido]penicillanic acid; D-(−)-α-Aminobenzylpenicillin sodium salt; Aminobenzylpenicillin sodium salt
Application Notes Ampicillin sodium salt is used to select for ampicillin resistance in mutated and transformed cells. It is also described for the use of inhancing luminol chemiluminescence.
Base Catalog Number 19419950
Beilstein Registry Number 4119211
Biochemical Physiological 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.
CAS # 69-52-3
EC Number 200-708-1
Format Powder
Grade molecular biology reagent, γ-irradiated
Hazard Statements H317-H334
Molecular Formula C16H18N3NaO4S
Molecular Weight 371.387 g/mol
Pack Size 50 mg
Personal Protective Equipment Dust mask, Eyeshields, Faceshields, Gloves
pKa At 25 °C ,pKa = 2.5 (-COOH),pKa = 7.3 (-NH2) (Lit.)
Potency ≥800 µg/mg
RTECS Number XH8400000
Safety Symbol GHS08
Sterility γ-Irradiated
Sterilization of Solutions Autoclaving solutions of ampicillin will destroy activity. Solutions can be sterilized by filtration (0.22 um filter) and stored frozen (-20 °C or below). Frozen solutions can be stored for up to 3 months.
Typical Working Concentration 100 mg/liter for both gram positive and gram negative bacteria
Usage Statement Research Use Only (RUO). Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Citations