CAS Number61336-70-7
SynonymsAmoxicillin Trihydrate; Amoxycillin trihydrate; MFCD00072029; AmoxicillinTrihydrate; Amoxicillin (trihydrate)
Molecular FormulaC16H25N3O8S
Molecular Weight419.45
Purity98%
Density1.54g/cm3
Boiling Point743.2ºC at 760 mmHg Vapour
Melting Point>200ºC (dec.)
Appearancesolid
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 61336-70-7 |
| Catalog No. | 2A-9009178 |
| Chinese Name | 阿莫西林三水物 |
| Synonyms | Amoxicillin Trihydrate; Amoxycillin trihydrate; MFCD00072029; AmoxicillinTrihydrate; Amoxicillin (trihydrate) |
| Molecular Formula | C16H25N3O8S |
| Molecular Weight | 419.45 |
| Purity | 98 |
| Density | 1.54g/cm3 |
| Boiling Point | 743.2ºC at 760 mmHg Vapour |
| Melting Point | >200ºC (dec.) |
| Appearance | solid |
| Storage Condition | 2-8℃ |
| Application | Amoxicillin trihydrate is a mid-spectrum beta-lactam antibiotic. |
| HTC | 2941109200 |
| PubChem ID | 329823148 |
| MDL Number | MFCD00072029 |
| 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 |
| 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 |
| InChI Key | MQXQVCLAUDMCEF-CWLIKTDRSA-N |
| Beilstein/REAXYS | 7507120 |
| NACRES Code | NA.24 |
| UNSPSC | 41116107 |
| MSDS | msds/9178_1_61336_70_7.pdf |
| Bioactivity | Amoxicillin Trihydrate is a moderate- spectrum, bacteriolytic, β-lactam antibiotic.Target: AntibacterialAmoxicillin is a moderate-spectrum, bacteriolytic, β-lactam antibiotic in the aminopenicillin family used to treat bacterial infections caused by susceptible Gram-positive and Gram-negative microorganisms. It is usually the drug of choice within the class because it is better-absorbed, following oral administration, than other β-lactam antibiotics. Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, which are resistant to a narrow spectrum of β-lactam antibiotics, such as penicillin. For this reason, it is often combined with clavulanic acid, a β-lactamase inhibitor. This increases effectiveness by reducing its susceptibility to β-lactamase resistance. From Wikipedia. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. http://en.wikipedia.org/wiki/Amoxicillin Chemical & Physical Properties Density 1.54g/cm3 Boiling Point 743.2ºC at 760 mmHg Vapour Melting Point >200ºC (dec.) Molecular Formula C16H25N3O8S Molecular Weight 419.450 Flash Point 403.3ºC Exact Mass 419.136230 PSA 185.95000 LogP 0.85990 Index of Refraction 302 ° (C=0.1, H2O) InChIKey AIPFZZHNBUVELL-YWUHCJSESA-N SMILES CC1(C)SC2C(NC(=O)C(N)c3ccc(O)cc3)C(=O)N2C1C(=O)O.O |
| Use of | Amoxicillin Trihydrate is a moderate- spectrum, bacteriolytic, β-lactam antibiotic.Target: AntibacterialAmoxicillin is a moderate-spectrum, bacteriolytic, β-lactam antibiotic in the aminopenicillin family used to treat bacterial infections caused by susceptible Gram-positive and Gram-negative microorganisms. It is usually the drug of choice within the class because it is better-absorbed, following oral administration, than other β-lactam antibiotics. Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, which are resistant to a narrow spectrum of β-lactam antibiotics, such as penicillin. For this reason, it is often combined with clavulanic acid, a β-lactamase inhibitor. This increases effectiveness by reducing its susceptibility to β-lactamase resistance. From Wikipedia. Properties Articles105 Name amoxicillin trihydrate Synonym More Synonyms Amoxicillin Trihydrate Biological Activity Description Amoxicillin Trihydrate is a moderate- spectrum, bacteriolytic, β-lactam antibiotic.Target: AntibacterialAmoxicillin is a moderate-spectrum, bacteriolytic, β-lactam antibiotic in the aminopenicillin family used to treat bacterial infections caused by susceptible Gram-positive and Gram-negative microorganisms. It is usually the drug of choice within the class because it is better-absorbed, following oral administration, than other β-lactam antibiotics. Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, which are resistant to a narrow spectrum of β-lactam antibiotics, such as penicillin. For this reason, it is often combined with clavulanic acid, a β-lactamase inhibitor. This increases effectiveness by reducing its susceptibility to β-lactamase resistance. From Wikipedia. Related Catalog Signaling Pathways >> Anti-infection >> Bacterial Research Areas >> Infection References [1]. http://en.wikipedia.org/wiki/Amoxicillin Chemical & Physical Properties Molecular Formula C16H25N3O8S Exact Mass 419.136230 PSA 185.95000 LogP 0.85990 InChIKey AIPFZZHNBUVELL-YWUHCJSESA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified |
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