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Technology Process of AMBERLITE(R) IRA-400 (CL)

AMBERLITE(R) IRA-400 (CL)

Base Information
  • Chemical Name:AMBERLITE(R) IRA-400 (CL)
  • CAS No.:9002-24-8
  • Molecular Formula:(C12H18NCl)n
  • Molecular Weight:0
  • Hs Code.:
AMBERLITE(R) IRA-400 (CL)

Synonyms:Borohydride on polymer support;

Suppliers and Price of AMBERLITE(R) IRA-400 (CL)
Supply Marketing:
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
  • Biosynth Carbosynth
  • Amberlite|r IRA-400(Cl), ion exchange resin
  • 2 Kg
  • $ 550.00
  • Biosynth Carbosynth
  • Amberlite|r IRA-400(Cl), ion exchange resin
  • 1 Kg
  • $ 350.00
  • Biosynth Carbosynth
  • Amberlite|r IRA-400(Cl), ion exchange resin
  • 500 g
  • $ 200.00
  • Biosynth Carbosynth
  • Amberlite|r IRA-400(Cl), ion exchange resin
  • 250 g
  • $ 125.00
  • Biosynth Carbosynth
  • Amberlite|r IRA-400(Cl), ion exchange resin
  • 100 g
  • $ 100.00
Total 32 raw suppliers
Chemical Property of AMBERLITE(R) IRA-400 (CL)
Chemical Property:
  • PSA：0.00000 
  • LogP:0.00000 
  • Water Solubility.:Insoluble in water. 
Purity/Quality:

99.9% *data from raw suppliers

Amberlite|r IRA-400(Cl), ion exchange resin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:
Useful:
  • General Description AMBERLITE(R) IRA-400 (CL) is a strongly basic anion exchange resin used as a catalyst or reagent support in synthetic chemistry, particularly for facilitating efficient one-pot reactions under mild conditions. In the context of the described study, it played a key role in the high-yield synthesis of dithiocarbazates from alcoholic tosylates and hydrazines, demonstrating its utility in simplifying reaction workflows and improving yields in organic transformations. Its basic properties and polymer-supported structure make it suitable for mediating reactions involving carbon disulfide and nucleophilic substitutions.
Refernces

An Efficient, basic resin-mediated, one-pot synthesis of dithiocarbazates through alcoholic tosylates

10.1080/10426500802203137

The research details an efficient, basic resin-mediated, one-pot synthesis of dithiocarbazates through alcoholic tosylates. The purpose of this study was to develop a quick and efficient method for synthesizing dithiocarbazates, which are compounds with significant medicinal, industrial, and synthetic applications. The researchers utilized a system involving Amberlite IRA 400 (a basic resin) and carbon disulfide (CS2) to react with various alcoholic tosylates of primary, secondary, and tertiary alcohols and substituted hydrazines. The process resulted in high yields of dithiocarbazates (80–98%) under mild reaction conditions and with simpler work-up procedures compared to previously reported methods.

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