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Isoconazole

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Isoconazole manufacturers

  • Isoconazole USP/EP/BP
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  • $1.10 / 1g
  • 2021-07-20
  • CAS:27523-40-6
  • Min. Order: 1g
  • Purity: 99.9%
  • Supply Ability: 100 Tons Min
  • Isoconazole
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  • $0.01 / 1KG
  • 2020-05-13
  • CAS:27523-40-6
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50 tons
Isoconazole Basic information
Product Name:Isoconazole
Synonyms:1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]- (9CI);Imidazole, 1-[2,4-dichloro-b-[(2,6-dichlorobenzyl)oxy]phenethyl]- (8CI);Isoconazole (base and/or unspecified salts);1-(2,4-Dichlorophenyl)-1-[(2,6-dichlorophenyl)methoxy]-2-(1H-imidazole-1-yl)ethane;1-[2-(2,4-Dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-1H-imidazole;1-[2-(2,6-Dichlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole;1-[β-[(2,6-Dichlorobenzyl)oxy]-2,4-dichlorophenethyl]-1H-imidazole;1H-Imidazole, 1-(2-(2,4-dichlorophenyl)-2-((2,6-dichlorophenyl)methoxy)ethyl)-
CAS:27523-40-6
MF:C18H14Cl4N2O
MW:416.13
EINECS:248-508-3
Product Categories:
Mol File:27523-40-6.mol
Isoconazole Structure
Isoconazole Chemical Properties
Boiling point 555.1±50.0 °C(Predicted)
density 1.40±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility Practically insoluble in water, very soluble in methanol, freely soluble in ethanol (96 per cent).
pka6?+-.0.12(Predicted)
CAS DataBase Reference27523-40-6
Safety Information
MSDS Information
Isoconazole Usage And Synthesis
Chemical PropertiesWhite or almost white powder.
OriginatorFazol,Fournier,France,1979
UsesAntibacterial; antifungal.
DefinitionChEBI: 1-{2-[(2,6-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl}imidazole is a member of the class of imidazoles that carries a 2-[(2,6-dichlorobenzyl)oxy]-2-(2,4-dichlorophenyl)ethyl group at position 1. It is a dichlorobenzene, an ether and a member of imidazoles.
IndicationsTopical treatment of mycoses of the skin induced or sustained by fungi such as dermatophytes and yeasts. In addition, isoconazole is indicated for therapy of vulvovaginal mycoses causes by Candida species and Candida (Torulopsis) glabrata.
Manufacturing ProcessTo a stirred and refluxing solution of 40 parts of benzene and 35 parts of dimethylformamide (both solvents previously dried azeotropically) are added successively 1.6 parts of sodium hydride and 7.7 parts of α-(2,4- dichlorophenyl)imidazole-1-ethanol, (cooling on ice is necessary). After the addition is complete, stirring and refluxing is continued for 30 minutes. Then there are added 7.8 parts of 2.6-dichlorobenzyl chloride and the whole is stirred at reflux for another 3 hours. The reaction mixture is poured onto water and the product 1-[2,4-dichloro-b-(2,6-dichlorobenzyloxy)phenethyl] imidazole, is extracted with benzene. The extract is washed twice with water, dried, filtered and evaporated in vacuo. The base residue is dissolved in a mixture of acetone and diisopropyl ether and to this solution is added an excess of concentrated nitric acid solution. The precipitated nitrate salt is filtered off and recrystallized from a mixture of methanol and diisopropyl ether, yielding 1-[2,4-dichloro-b-(2,6-dichlorobenzyloxy)phenethyl]imidazole nitrate; melting point 179°C.
Therapeutic FunctionAntibacterial, Antifungal
Antimicrobial activityBroad-spectrum azole antimycotic with activity against almost all species of pathogenic fungi.
PharmacokineticsAfter topical application, isoconazole remains practically unabsorbed. Application in an ethanol/propyleneglycol vehicle increases penetration into the stratum corneum of the skin significantly.
Side effectsLocal irritations such as itching and burning sensations and allergic reactions may occur in rare cases and are mainly due to the galenic formulation.
Solubility in organicsIsoconazole is soluble in methanol, acetic acid, and PEG 400; less soluble in ethanol, acetone, chloroform, and butanol; and barely soluble in water, diethyl ether, cyclohexane, and hexane.
Tag:Isoconazole(27523-40-6) Related Product Information
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