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Isoconazole nitrate

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Products Intro: Product Name:Isoconazole nitrate
CAS:24168-96-5
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CAS:24168-96-5
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CAS:24168-96-5
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Isoconazole nitrate manufacturers

  • Isoconazole nitrate
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  • $30.00 / 25mg
  • 2025-11-04
  • CAS:24168-96-5
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  • Purity: 99.73%
  • Supply Ability: 10g
  • Isoconazole Nitrate
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  • $150.00 / 1kg
  • 2025-05-23
  • CAS:24168-96-5
  • Min. Order: 1kg
  • Purity: 99%
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  • Isoconazole nitrate
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  • $1.00 / 1KG
  • 2025-05-14
  • CAS:24168-96-5
  • Min. Order: 1KG
  • Purity: 99%
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Isoconazole nitrate Basic information
Product Name:Isoconazole nitrate
Synonyms:1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-1h-imidazole mononitrate;1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-1H-imidazolium nitrate;1H-Imidazole, 1-[2-(2,4-dichlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]-, mononitrate (9CI);Adestan G 100;Fazol;Gyno-Travogen;Imidazole, 1-[2,4-dichloro-b-[(2,6-dichlorobenzyl)oxy]phenethyl]-, mononitrate (8CI);R 15454
CAS:24168-96-5
MF:C18H15Cl4N3O4
MW:479.14
EINECS:246-051-4
Product Categories:Inhibitors;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Antifungal
Mol File:24168-96-5.mol
Isoconazole nitrate Structure
Isoconazole nitrate Chemical Properties
Melting point 178-182°C
storage temp. Sealed in dry,2-8°C
solubility Very slightly soluble in water, soluble in methanol, slightly soluble in ethanol (96 per cent).
form Solid
color White to Off-White
Merck 14,5160
CAS DataBase Reference24168-96-5(CAS DataBase Reference)
Safety Information
RIDADR UN3077
RTECS NI4772000
HS Code 2933.29.4300
HazardClass 9
MSDS Information
Isoconazole nitrate Usage And Synthesis
Chemical PropertiesWhite Solid
OriginatorFazol,Fournier,France,1979
UsesAntibacterial; antifungal
UsesIsoconazole Nitrate acts as an antibacterial in the local treatment of vaginitis; antifungal agent (1,2).
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
Isoconazole nitrate Preparation Products And Raw materials
Raw materialsSodium hydride
Tag:Isoconazole nitrate(24168-96-5) Related Product Information
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