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Amoxicillin trihydrate

Art.No A-030
Formula C16H19N3O5S
Conc (% w/w) 10.0% pet
Series CAD
Molality -
MW 365,4
CAS 26787-78-0
Download Safety Data Sheet
Hapten Information
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[2S-[2alpha,5alpha,6beta(S*)]]-6-[[2-amino-2-(4-hydroxyphenyl) acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; p-Hydroxyampicillin; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-(2-amino-2-(p-hydroxyphenyl)acetamido)-3,3-dimethyl-7-oxo, D-; 6-; (-)-6-[2-amino-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; 6-(p-Hydroxy-alpha-aminophenylacetamido) pencillanic acid; 6-(p-hydroxy-alpha-aminophenylacetamido)penicillanic acid; 6-(D-(-)-p-Hydroxy-alpha-aminobenzyl)penicillin; 6-[D(-)-alpha-amino-p-hydroxyphenylacetamido]penicillanic acid; alpha-amino-p-hydroxybenzyl penicillin; Alphacin; Agram (Trihydrate); Alfamox; Almodan; Amocilline; Amoclen; Amodex (Trihydrate); Amolin; Amopen; Amopenixin; Alphamox; Amoxi; Amoxidin (Trihydrate); Amoxibiotic (Trihydrate); Amoxicilline; Amoxicillin trihydrate; Amoxidal (Trihydrate); Amoxil; Amoxil (Trihydrate); Amoxillat (Trihydrate); Amoxipen; Amoxi-Wolff (Trihydrate); Amoxycillin; Amoxypen (Trihydrate); AMPC; Anemolin; Aspenil; Augmentin; Betamox; Bristamox; Cabermox; Cemoxin; Cilamox; Clamoxyl; Clamoxyl (Trihydrate); Cuxacillin; D-(-)-alpha-amino-p-hydroxybenzyl penicillin trihydrate; Delacillin; Efpenix; Fisamox; Grinsil; Histocillin; Ibiamox; Imacillin; Larotid; Moxacin; Optium; Ospamox; Piramox; Polymox; Sawacillin; Sawacillin (Trihydrate); Simoxil; Sumox; Trimox; Trimox (Trihydrate); Utimox; Wymox (Trihydrate);


Amoxicillin or amoxycillin is a moderate-spectrum beta-lactam antibiotic used to treat bacterial infections caused by susceptible microorganisms. It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other beta-lactam antibiotics. Amoxicillin is susceptible to degradation by beta-lactamase-producing bacteria, and so may be given with clavulanic acid to decrease its susceptibility. It was developed by Beecham in 1972 and is currently marketed by GlaxoSmithKline (the inheritor company) under the original trade name Amoxil.

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