7177-48-2
- Product Name:Ampicillin
- Molecular Formula:C16H19N3O4S.3(H2O)
- Purity:99%
- Molecular Weight:
Product Details
Appearance:Odorless white microcrystalline powder with a bitter taste
Ampicillin7177-48-2 superior manufacturer, factory sells
- Molecular Formula:C16H19N3O4S*3H2O
- Molecular Weight:403.456
- Appearance/Colour:Odorless white microcrystalline powder with a bitter taste
- Vapor Pressure:1.21E-19mmHg at 25°C
- Melting Point:208 °C (dec.)(lit.)
- Refractive Index:265 ° (C=0.1, H2O)
- Boiling Point:683.9 °C at 760 mmHg
- PKA:2.5 (COOH)(at 25℃)
- Flash Point:367.4 °C
- PSA:165.72000
- LogP:1.15430
7177-48-2 Usage
Ampicillin (AMP) is an antibiotic belonging to the β-lactam group, which exhibits a broad spectrum of action in preventing and treatment of various bacterial diseases. As a penicillin group of beta-lactam antibiotics, Ampicillin is the first broad-spectrum penicillin, which has in vitro activity against Gram-positive and Gram-negative aerobic and anaerobic bacteria, commonly used for preventing and treating bacterial infections of respiratory tract, bladder, and kidney, etc. caused by susceptible bacteria. It is also used to treat uncomplicated gonorrhea, meningitis, endocarditis salmonellosis, and other serious infections through administered by mouth, intramuscular injection or by intravenous infusion. Ampicillin usually is given intravenously (IV) or intramuscularly (IM), whereas amoxicillin is the preferred oral agent because it is less likely to cause diarrhea and can be administered less frequently than oral ampicillin.
Safety Profile
Mildly toxic by ingestion. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of SO,xand NOx.
Shipping
UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.
InChI:InChI=1/C16H19N3O4S.3H2O/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;;;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);3*1H2/t9-,10-,11+,14-;;;/m1.../s1
7177-48-2 Relevant articles
Capability of MXene 2D material as an amoxicillin, ampicillin, and cloxacillin adsorbent in wastewater
Ahmad Miri-Jahromi, Mohsen Didandeh, Sina Shekarsokhan
, Journal of Molecular Liquids Volume 351, 1 April 2022, 118545
Amoxicillin, ampicillin, and cloxacillin are three semi-synthetic antibiotic compounds that pollute wastewaters.
Degradation of ampicillin by combined process: Adsorption and Fenton reaction
Cassandra Bonfante de Carvalho, Ivan Reis Rosa, Paola Del Vecchio, Ivone Vanessa Jurado Dávila, Keila Guerra Pacheco Nunes, Nilson Romeu Marcilio, Liliana Amaral Féris
Environmental Technology & Innovation Volume 26, May 2022, 102365
In this context, the present work investigated the degradation and mineralization of the -lactam antibiotic ampicillin (AMP) applying a combined treatment of Fenton reaction and adsorption onto granular activated carbon (GAC).
7177-48-2 Process route
- 660-68-4
diethyl amine hydrochloride
- 5187-94-0,7177-48-2,32388-53-7,57095-77-9,145454-26-8
ampicillin trihydrate
Conditions | Yield |
---|---|
|
- 57397-48-5
N,N-Bis(trimethylsilyl)urea
- 551-16-6
6-Aminopenicillanic Acid
- 5187-94-0,7177-48-2,32388-53-7,57095-77-9,145454-26-8
ampicillin trihydrate
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; triethylamine; In dichloromethane;
|
87.6% |
7177-48-2 Upstream products
-
551-16-6
6-aminopenicillanic acid
-
5321-31-3
phenylglycidylchloride hydrochloride
-
551-16-6
6-Aminopenicillanic Acid
-
18297-63-7
N,N'-bis(trimethylsilyl)urea
7177-48-2 Downstream products
-
87-53-6
penicillanic acid
-
61-33-6
penicillin G
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