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Ampicillin Sodium Salt

Ampicillin Sodium Salt

Synonyms D[-]-a-Aminobenzylpenicillin; 6-[D(-)-a-Aminophenylacetamido]penicillanic acid

CAS Number: 69-52-3 Molecular Formula: C16H18N3O4SNa Molecular Weight: 371.387 g/mol

Beilstein Registry Number: 4119211 EC Number: 200-708-1 MDL Number: MFCD00064313

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SKU 02194526-CF
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Description

Product Description

Ampicillin Sodium Salt

Application Notes

Ampicillin is a semi-synthetic derivative of penicillin that functions as a broad-spectrum antibiotic. It has been used to study antibiotic resistance and penetration limitations, the synergy between multiple antibiotics, certain bloodstream infections, and has been used to develop PCR assays to detect resistance genes in cerebrospinal fluid. Also described for the use of enhancing 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

Specifications
SKU 02194526-CF
Application Notes Ampicillin is a semi-synthetic derivative of penicillin that functions as a broad-spectrum antibiotic. It has been used to study antibiotic resistance and penetration limitations, the synergy between multiple antibiotics, certain bloodstream infections, and has been used to develop PCR assays to detect resistance genes in cerebrospinal fluid. Also described for the use of enhancing luminol chemiluminescence.
Beilstein Registry Number 4119211
Biochemical Physiological Actions Mode of Action: This is a ß-lactam antibiotic that inhibits bacterial cell-wall synthesis by inactivating transpeptidases on the inner surface of the bacterial cell membrane.Mode of Resistance: Administration with ß-lactamase cleaves the ß-lactam ring of Ampicillin and inactivates it. Antimicrobial Spectrum: Includes both gram-positive (similar to benzylpenicillin) and gram-negative bacteria (similar to tetracyclines and chloramphenicol.
EC Number 200-708-1
Grade Cell Culture Reagent
Hazard Statements H317-H334
Applications Antibiotic
Molecular Formula C16H18N3O4SNa
Molecular Weight 371.387 g/mol
Personal Protective Equipment Dust mask , Eyeshields, Faceshields, Gloves
Physical Appearance White Powder
pKa 2.5 (-COOH), pKa = 7.3 (-NH2)
Potency ≥800 µg/mg
Product Families Description Ampicillin
Product Overview Ampicillin Sodium Salt
RTECS Number XH8400000
Storage and Handling Store at +4 °C.
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.