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INDIUM(III) PHTHALOCYANINE CHLORIDE

Base Information Edit
  • Chemical Name:INDIUM(III) PHTHALOCYANINE CHLORIDE
  • CAS No.:19631-19-7
  • Molecular Formula:C32H16ClInN8
  • Molecular Weight:662.794
  • Hs Code.:
  • Mol file:19631-19-7.mol
INDIUM(III) PHTHALOCYANINE CHLORIDE

Synonyms:Indium(III) phthalocyanine chloride;

Suppliers and Price of INDIUM(III) PHTHALOCYANINE CHLORIDE
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
  • Sigma-Aldrich
  • Indium(III) phthalocyanine chloride Dye content 95 %
  • 1g
  • $ 327.00
  • Sigma-Aldrich
  • Indium(III) phthalocyanine chloride Dye content 90 %
  • 1g
  • $ 196.00
Total 9 raw suppliers
Chemical Property of INDIUM(III) PHTHALOCYANINE CHLORIDE Edit
Chemical Property:
  • Melting Point:>300 °C 
  • PSA:84.02000 
  • LogP:2.15390 
Purity/Quality:

98%,99%, *data from raw suppliers

Indium(III) phthalocyanine chloride Dye content 95 % *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Sensitizer for electrophotography
Technology Process of INDIUM(III) PHTHALOCYANINE CHLORIDE

There total 6 articles about INDIUM(III) PHTHALOCYANINE CHLORIDE 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:
In quinoline; under exclusion of water; mixt. of phthalonitrile, anhyd. InCl3 and distd. deoxygenated quinoline refluxed for 1 h; cooled to ca. 273 K; filtered; washed with toluene and MeOH; dried at 383 K; elem. anal.;
DOI:10.1016/j.poly.2010.12.047
Guidance literature:
In α-chloronaphthalene; at 200 ℃; for 13h;
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In pentan-1-ol; at 136 ℃; for 7h;
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