Sodium cloxacillin

Sodium cloxacillin
Sodium cloxacillin
Sodium cloxacillin

Sodium cloxacillin

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1 Metric Ton

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  • Min.Order :1 Metric Ton
  • Purity: 98%
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Keywords

Sodium cloxacillin 642-78-4 C19H17ClN3O5S.Na

Quick Details

  • Appearance:white crystalline powder
  • Application:642-78-4
  • PackAge:As requested
  • ProductionCapacity:300|Metric Ton|Day
  • Storage:keep in dry and ventilated
  • Transportation:By air or by sea

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Sodium cloxacillin Basic information
Product Name: Sodium cloxacillin
Synonyms: 3-dimethyl-7-oxo-thyl-4-isoxazolecarboxamido)-monosodiumsalt;3-o-chlorophenyl-5-methyl-4-isoxazolylpenicillinsodium;ankerbin;austrastaph;brl-1621sodiumsalt;cloxapen;ekvacillin;gelstaph
CAS: 642-78-4
MF: C19H17ClN3O5S.Na
MW: 457.87
EINECS: 211-390-9
Product Categories: A - KAntibiotics;Antibacterial;Antibiotics A to;Antibiotics A-FAntibiotics;Chemical Structure Class;Interferes with Cell Wall SynthesisAntibiotics;Mechanism of Action;Penicillins and Cephalosporins (beta-Lactams);Spectrum of Activity;Amines;Aromatics;Chiral Reagents;Heterocycles;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;API
Mol File: 642-78-4.mol
Sodium cloxacillin Structure
 
Sodium cloxacillin Chemical Properties
mp  170°C
storage temp.  2-8°C
solubility  H2O: 50 mg/mL, clear, colorless
Stability: Stable. Incompatible with strong oxidizing agents. Refrigerate.
CAS DataBase Reference 642-78-4(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn
Risk Statements  36/37/38-42/43
Safety Statements  26-36-22
WGK Germany  2
RTECS  XH8920000
 
Sodium cloxacillin Usage And Synthesis
Chemical Properties White Crystalline Powder
Usage Cloxacillin is an antibiotic that belongs to the group of the isoxazolylpenicillins. Cloxacillin is used to treat infections caused by species of staphylococci that produce beta-lactamase due to its inhibitory effects on beta-lactamase binding.
Usage Labelled analogue of Cloxacillin, an antibiotic that belongs to the group of the isoxazolylpenicillins. Cloxacillin is used to treat infections caused by species of staphylococci that produce beta-lac tamase due to its inhibitory effects on beta-lactamase binding.
Usage Labelled S-Form of Dropropizine. Cough suppressive phenylpiperazine derivative. Antitussive.
Usage Ropivacaine (R675000) metabolite.
 
Sodium cloxacillin Preparation Products And Raw materials
Preparation Products Cloxacillin sodium

 

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