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Dibenzofuran, 1,3,4,8-tetrachloro-

Base Information Edit
  • Chemical Name:Dibenzofuran, 1,3,4,8-tetrachloro-
  • CAS No.:92341-04-3
  • Molecular Formula:C12H4Cl4O
  • Molecular Weight:305.975
  • Hs Code.:2932999099
  • Mol file:92341-04-3.mol
Dibenzofuran, 1,3,4,8-tetrachloro-

Synonyms:1,3,4,8-TCDF;1,3,4,8-Tetrachlorodibenzofuran; PCDF 66

Suppliers and Price of Dibenzofuran, 1,3,4,8-tetrachloro-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • 1,3,4,8-TETRACHLORODIBENZOFURAN 95.00%
  • 5MG
  • $ 504.55
Total 3 raw suppliers
Chemical Property of Dibenzofuran, 1,3,4,8-tetrachloro- Edit
Chemical Property:
  • Vapor Pressure:9.93E-07mmHg at 25°C 
  • Boiling Point:415.4°Cat760mmHg 
  • Flash Point:205.1°C 
  • PSA:13.14000 
  • Density:1.625g/cm3 
  • LogP:6.19960 
Purity/Quality:

1,3,4,8-TETRACHLORODIBENZOFURAN 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 1,3,4,8-Tetrachlorodibenzofuran isa standard used for environmental testing and research used in the study of dioxin contaminants in natural lakes and rivers.
Technology Process of Dibenzofuran, 1,3,4,8-tetrachloro-

There total 3 articles about Dibenzofuran, 1,3,4,8-tetrachloro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With water; oxygen; fly ash; at 298 - 398 ℃; Further byproducts given. Title compound not separated from byproducts; Formation of xenobiotics;
DOI:10.1021/es971077z
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