Ampicillin, sodium salt

Name: Ampicillin, sodium salt
SKU: 02194526-CF
Price: 135 EUR

€135.00

Key features and details

Ampicillin Sodium Salt

SKU: 02194526-CF

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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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.