Ampicillin sodium
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Ampicillin sodium
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CAS No:
69-52-3
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Formula:
C16H19N3O4S.Na
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Chemical Name:
Ampicillin sodium
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Synonyms:
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-,sodium salt (1:1),(2S,5R,6R)-;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-,monosodium salt,D-(-)-;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-,monosodium salt,[2S-[2α,5α,6β(S*)]]-;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid,6-[[(2R)-aminophenylacetyl]amino]-3,3-dimethyl-7-oxo-,monosodium salt,(2S,5R,6R)-;Ampicillin sodium;Penbritin S;Sodium P-50;Sodium 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate;Sodium 6-[D-α-aminophenylacetamido]penicillanoate;Sodium ampicillin;Ampicillin sodium salt;Binotal sodium;Sodium D-α-aminobenzylpenicillanate;Sodium binotal;D-α-Aminobenzylpenicillin sodium salt;Polycillin N;Monosodium ampicillin;Ampicillin-Na;Anhypen;Britapen injection;Sodium ampicillinate;Ampicin;Principen N;Omnipen N;Alpen N;Pen A/N;Amcill S;Pentrex;Cilleral;Ampi-Dry 5000;Solampi;Pamecil;Totacillin N;24863-47-6;57748-55-7
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CAS No:
Description
Ampicillin sodium is a broad-spectrum beta-lactam antibiotic against a variety of gram-positive and gram-negative bacteria.
Characteristics
138
1.35
white with slight yellow cast powder
215 °C (dec.)(lit.)
683.9°C at 760 mmHg
Freely soluble in water. Sparingly soluble in acetone;H2O: 50 mg/mL, clear, very faintly yellow
2-8°C
Oral-Rat LD50:> 5314 mg/kg; Oral-Mouse LD50:> 5314 mg/kg
Combustion produces toxic sodium oxide, nitrogen oxide and sulfur oxide gas
Optical rotation = +287.9 deg at 20 °C (C=1 in H2O)
Odorless or has a faint odor characteristic of the penicillins
Safety Information
Ⅲ
2811
2
42/43-36/37/38-22
22-36/37-45-36-26
XH8400000
Xi,Xn
Warehouse ventilated, low temperature and dry
The stability of ampicillin sodium in soln is concn dependent and decreased as the concn of the drug increases. Ampicillin sodium appears to be especially susceptible to inactivation in soln containing dextrose, which appears to have a catalytic effect on hydrolysis of the drug.
P261-P280-P342 + P311
H317-H334
Ampicillin sodium Use and Manufacturing
Derived from ampicillin salt: Suspend ampicillin in water, adjust pH to 9 with sodium hydroxide solution, dissolve, and filter. The filtrate is decolorized with activated carbon, filtered, and the filtrate is dried at low temperature to obtain a product.
diuretic, anti-hypertensive
Drug Function and Efficacy
Broad-spectrum semi-synthetic penicillin has a broad-spectrum killing effect on gram-positive and gram-negative bacteria. It has a strong antibacterial effect on hemolytic streptococci, pneumococci and non-penicillinase-producing staphylococci, which is similar to or slightly inferior to penicillin. It also has a good antibacterial effect on viridans streptococci, and is better than penicillin on enterococci and listeria. It is effective against Corynebacterium diphtheriae, Bacillus anthracis, Actinomyces, Haemophilus influenzae, Bordetella pertussis and Neisseria.
Registered Holders
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North China Pharmaceutical Group Semisyntech Co.,Ltd.
Active
Japan
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Sandoz GmbH
Active
Austria
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ACS DOBFAR S. P. A.
Active
Brazil
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