7177-48-2

  • Product Name:Ampicillin
  • Molecular Formula:C16H19N3O4S.3(H2O)
  • Purity:99%
  • Molecular Weight:
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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

diethyl amine hydrochloride
660-68-4

diethyl amine hydrochloride

ampicillin trihydrate
5187-94-0,7177-48-2,32388-53-7,57095-77-9,145454-26-8

ampicillin trihydrate

Conditions
Conditions Yield
 
 
N,N-Bis(trimethylsilyl)urea
57397-48-5

N,N-Bis(trimethylsilyl)urea

6-Aminopenicillanic Acid
551-16-6

6-Aminopenicillanic Acid

ampicillin trihydrate
5187-94-0,7177-48-2,32388-53-7,57095-77-9,145454-26-8

ampicillin trihydrate

Conditions
Conditions Yield
With chloro-trimethyl-silane; triethylamine; In dichloromethane;
87.6%

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7177-48-2 Downstream products

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