Products for Research Use Only

Amoxicillin trihydrate

CAT: 0013-GTR19177678-02Size: 1 gDry Ice: NoHazardous: No
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CAT#:0013-GTR19177678-02Size:1 g
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Description
Amoxicillin trihydrate is a semisynthetic, broad-spectrum bactericidal antibiotic. It inactivates penicillin-binding proteins like PBP-1A, disrupting peptidoglycan cross-linking in the bacterial cell wall, leading to cell lysis. This compound is widely used in microbiological research for in vitro susceptibility testing and in vivo models of bacterial infection.
CAS Number
61336-70-7
Product Name Alternative
Inhibitor, PBPs, inhibit, Moxaline, Moxaline Trihydrate, Moxaline trihydrate, cell wall, Bacterial, Amoxicillin Trihydrate, Amoxicillin trihydrate, Amoxil, Amoxil trihydrate, Amoxil Trihydrate, Amoxipen, Amoxipen Trihydrate, Amoxipen trihydrate, Amoxycillin, Amoxycillin Trihydrate, Amoxycillin trihydrate, Amoxicillin, Antibiotic, antimicrobial, polypeptides
Field of Research
Infectious Disease & Virology, Pharmacology & Drug Discovery
Purity
98.90% (May vary between batches)
Solubility
DMSO:60 mg/mL (143.04 mM) ; H2O:1.25 mg/mL (2.98 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (2.38 mM)
Smiles
O.O.O.CC1 (C) S[C@@H]2[C@H] (NC (=O) [C@H] (N) c3ccc (O) cc3) C (=O) N2[C@H]1C (O) =O
Molecular Formula
C16H25N3O8S
Molecular Weight
419.45
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

Amoxicillin Trihydrate

Amoxicillin trihydrate is a hydrate that is the trihydrate form of amoxicillin; a semisynthetic antibiotic, used either alone or in combination with potassium clavulanate (under the trade name Augmentin) for treatment of a variety of bacterial infections. It has a role as an antimicrobial agent and an antibacterial drug. It contains an amoxicillin.

CAS Number61336-70-7
PubChem CID62883
IUPAC Name(2S,5R,6R)-6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid;trihydrate
Molecular FormulaC16H25N3O8S
Molecular Weight419.5
Topological Polar Surface Area161
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count10
Rotatable Bond Count4
Heavy Atom Count28
Formal Charge0
Complexity590
SMILES
CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=C(C=C3)O)N)C(=O)O)C.O.O.O
InChI
InChI=1S/C16H19N3O5S.3H2O/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7;;;/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24);3*1H2/t9-,10-,11+,14-;;;/m1.../s1
InChIKey
MQXQVCLAUDMCEF-CWLIKTDRSA-N
Chemical Structure
2D Structure
2D structure of Amoxicillin Trihydrate
CAS: 61336-70-7
CID: 62883
Formula: C16H25N3O8S
MW: 419.5
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight419.5
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count10
Rotatable Bond Count4
Exact Mass419.13623594
Monoisotopic Mass419.13623594
Topological Polar Surface Area161 Ų
Heavy Atom Count28
Formal Charge0
Complexity590
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count4
Compound Is CanonicalizedYes