![]() Amoxicillin Trihydrate structure
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Common Name | Amoxicillin Trihydrate | ||
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CAS Number | 61336-70-7 | Molecular Weight | 419.450 | |
Density | 1.54g/cm3 | Boiling Point | 743.2ºC at 760 mmHg Vapour | |
Molecular Formula | C16H25N3O8S | Melting Point | >200ºC (dec.) | |
MSDS | Chinese USA | Flash Point | 403.3ºC | |
Symbol |
![]() GHS08 |
Signal Word | Danger |
Use of Amoxicillin TrihydrateAmoxicillin 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. |
Name | amoxicillin trihydrate |
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Synonym | More Synonyms |
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. |
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Related Catalog | |
References |
Density | 1.54g/cm3 |
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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) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
![]() GHS08 |
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Signal Word | Danger |
Hazard Statements | H317-H334 |
Precautionary Statements | P261-P280-P342 + P311 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xn:Harmful |
Risk Phrases | R42/43 |
Safety Phrases | S36 |
RIDADR | NONH for all modes of transport |
RTECS | XH8300000 |
HS Code | 2941109200 |
HS Code | 2941109200 |
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Experimental study of the impact of antimicrobial treatments on Campylobacter, Enterococcus and PCR-capillary electrophoresis single-strand conformation polymorphism profiles of the gut microbiota of chickens.
J. Med. Microbiol. 63(Pt 11) , 1552-60, (2014) An experiment was conducted to compare the impact of antimicrobial treatments on the susceptibility of Campylobacter, Enterococcus faecium and Enterococcus faecalis, and on the diversity of broiler mi... |
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Chemical composition, antibacterial and antioxidant activities of six essentials oils from the Alliaceae family.
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Simultaneous determination of 38 veterinary antibiotic residues in raw milk by UPLC-MS/MS.
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4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)-, hydrate (1:3) |
(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 |
Amoxicillin Trihydrate |
Amoxycillin trihydrate |
MFCD00072029 |
AmoxicillinTrihydrate |
Amoxicillin (trihydrate) |