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

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

Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.

Key Applications

Antibiotic

Specifications
SKU 02194526-CF
Alternate Names D[-]-a-Aminobenzylpenicillin; 6-[D(-)-a-Aminophenylacetamido]penicillanic acid
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.
Base Catalog Number 194526
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.
CAS # 69-52-3
EC Number 200-708-1
Grade Cell Culture Grade
Hazard Statements H317-H334
Molecular Formula C16H18N3O4SNa
Molecular Weight 371.387 g/mol
Personal Protective Equipment Dust mask , Eyeshields, Faceshields, Gloves
pKa 2.5 (-COOH), pKa = 7.3 (-NH2)
Potency ≥800 µg/mg
RTECS Number XH8400000
Typical Working Concentration 100 mg/liter for both gram positive and gram negative bacteria.
Usage Statement Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department.