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Azaconazole

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Company Name: Hubei Jusheng Technology Co.,Ltd.
Tel: 18871490254
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Products Intro: Product Name:azaconazole
CAS:60207-31-0
Purity:99% Package:5KG;1KG Remarks:C12H11Cl2N3O2
Company Name: Hubei xin bonus chemical co. LTD
Tel: 86-13657291602
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Products Intro: Product Name:Azaconazole
CAS:60207-31-0
Purity:0.99 Package:5KG;1KG
Company Name: Chongqing Chemdad Co., Ltd
Tel: +86-023-6139-8061 +86-86-13650506873
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Products Intro: Product Name:Azaconazole
CAS:60207-31-0
Purity:0.99 Package:5KG;1KG,25KG
Company Name: CONIER CHEM AND PHARMA LIMITED
Tel: +8618523575427
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Products Intro: Product Name:azaconazole
CAS:60207-31-0
Purity:99% Package:1kg
Company Name: career henan chemical co
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Products Intro: Product Name:Azaconazole
CAS:60207-31-0
Purity:98% Package:1KG;3USD

Azaconazole manufacturers

  • Azaconazole
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  • $3.00 / 1KG
  • 2020-01-19
  • CAS:60207-31-0
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 1kg,5kg,50kg
Azaconazole Basic information
Product Name:Azaconazole
Synonyms:AZOCONAZOLE;1-[[2-(2,4-Dichlorophenyl)-1,3-dioxolan-2-yl]methyl]-1,2,4-triazole;SAFETRAY SL;RODEWOD;4-triazole,1-((2-(2,4-dichlorophenyl)-1,3-dioxolan-2-yl)methyl)-1h-2;azoconozole;madurox;AZACONAZOLE
CAS:60207-31-0
MF:C12H11Cl2N3O2
MW:300.14
EINECS:262-102-3
Product Categories:
Mol File:60207-31-0.mol
Azaconazole Structure
Azaconazole Chemical Properties
Melting point 109.9°
Boiling point 460.7±55.0 °C(Predicted)
density 1.51±0.1 g/cm3(Predicted)
vapor pressure 8.6 x l0-6 Pa (20 °C)
storage temp. 0-6°C
pka2.94±0.12(Predicted)
Water Solubility 300 mg l-1 (20 °C)
CAS DataBase Reference60207-31-0(CAS DataBase Reference)
EPA Substance Registry SystemAzaconazole (60207-31-0)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 46
WGK Germany 1
RTECS XZ4605000
HS Code 29349990
MSDS Information
Azaconazole Usage And Synthesis
OriginatorAzaconazole,Chemical
UsesAzaconazole is particularly active against wood-destroying and sapstain fungi. It is also used as a disinfectant in mushroom cultivation and on storage boxes for fruit and vegetables.
UsesFungicide for cultivation on wood; preservative for composite wood products.
DefinitionChEBI: A member of the class of dioxolanes that is 1,3-dioxolane substituted at position 2 by 2,4-dichlorophenyl and 1,2,4-triazol-1-ylmethyl groups. A fungicide used mainly in ornamental crops to control canker and other diseases. Azaconazole is moderately toxic to mammals but is not expected to bioaccumulate. It is moderately toxic to birds, fish and aquatic invertebrates.
Manufacturing ProcessA stirred and cooled (0°C) solution of 1-(2,4-diaminophenyl)-1-ethanone in a concentrated hydrochloric acid solution, water and acetic acid was diazotated with a solution of sodium nitrite in water. After stirring at 0°C, the whole was poured onto a solution of copper (I) chloride in a concentrated hydrochloric acid solution while stirring. The mixture was heated at 60°C. After cooling to room temperature, the product was extracted twice with 2,2'-oxybispropane. The combined extracts were washed successively with water, a diluted sodium hydroxide solution and again twice with water, dried, filtered and evaporated, yielding 1-(2,4-dichlorophenyl)-1-ethanone.
1-(2,4-Dichlorophenyl)-1-ethanon were dissolved in 1,2-ethanediol at heating. While stirring bromine were added dropwise, without external heating. After stirring at room temperature, 4-methylbenzenesulfonic acid and benzene were added. The whole was stirred and refluxed overnight with water-separator. The reaction mixture was evaporated and the residue was taken up in 2,2'- oxybispropane. The resulting solution was washed successively once with a dilute sodium hydroxide solution and 3 times with water, dried, filtered and evaporated. The residue was distilled, yielding 2-(bromomethyl)-2-(2,4- dichlorophenyl)-1,3-dioxolane.
6.9 parts of 1H-1,2,4-triazole in 150 parts of dimethylformamide were added to a stirred solution of 2.3 parts of sodium in 120 parts of methanol. The methanol was removed at normal pressure until the internal temperature of 130°C was reached. Then, 25 parts of 2-(bromomethyl)-2-(2,4- dichlorophenyl)-1,3-dioxolane were added. The reaction-mixture was stirred and refluxed for 3 h. It was allowed to cool to room temperature and poured onto water. The precipitated product was filtered off, yielding 12 parts of 1-[2- (2,4-dichlorophenyl)-1,3-dioxolan-2-yl-methyl]-1H-1,2,4-triazole, melting point 109.9°C (crystallized from diisopropylether, activated charcoal).
Therapeutic FunctionAntifungal
Metabolic pathwayLittle published dormation is available on the metabolism of azaconazole.
DegradationAzaconazole is stable to light under normal storage conditions (but not in ketonic solvents). It is stable at temperatures up to 220 °C.
Tag:Azaconazole(60207-31-0) Related Product Information
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