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POLYETHYLENE GLYCOL 4000 DIMESYLATE

Base Information Edit
  • Chemical Name:POLYETHYLENE GLYCOL 4000 DIMESYLATE
  • CAS No.:52410-74-9
  • Molecular Formula:
  • Molecular Weight:218.2486
  • Hs Code.:
  • Mol file:52410-74-9.mol
POLYETHYLENE GLYCOL 4000 DIMESYLATE

Synonyms:PEG4'000dimesylate;o,o'-dimesyl-polyethylene glycol;polyethylene glycol dimesylate;O,Oμ-Dimesyl-polyethylene glycol, O,Oμ-Dimethanesulfonyl-polyethylene glycol;Polyethylene glycol diMethanesulfonate, M.W. 8,000;Polyethylene glycol diMethanesulfonate, M.W. 1,000;Polyethylene glycol diMethanesulfonate, M.W. 3,400

Suppliers and Price of POLYETHYLENE GLYCOL 4000 DIMESYLATE
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
  • O,O'-DIMESYL-POLYETHYLENE GLYCOL 95.00%
  • 5MG
  • $ 504.70
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 1,000
  • 5g
  • $ 149.00
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 8,000
  • 5g
  • $ 149.00
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 1,000
  • 1g
  • $ 70.20
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 8,000
  • 1g
  • $ 69.40
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 1,000
  • 250mg
  • $ 12.90
  • Alfa Aesar
  • Polyethylene glycol dimethanesulfonate, M.W. 8,000
  • 250mg
  • $ 12.90
Total 5 raw suppliers
Chemical Property of POLYETHYLENE GLYCOL 4000 DIMESYLATE Edit
Chemical Property:
  • Melting Point:54-57 °C  
Purity/Quality:

98%Min *data from raw suppliers

O,O'-DIMESYL-POLYETHYLENE GLYCOL 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Polyethylene glycol is involved in the chemoselective synthesis of organic carbamates from amines, carbondioxides and alkyl halides. The presence of polyethylene glycol could also depress the alkylation of both the amine and the carbamate, thus resulting in enhanced selectivity toward the target carbamate during the synthesis.
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