Ethyltriphenylphosphonium iodide

95%

  • Product Code: 121964
  Alias:    Ethyltriphenylphosphine iodide
  CAS:    4736-60-1
Molecular Weight: 418.25 g./mol Molecular Formula: C₂₀H₂₀IP
EC Number: 225-245-2 MDL Number: MFCD00040352
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, away from light
Product Description: Ethyltriphenylphosphonium iodide is widely used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It is particularly effective in nucleophilic substitution reactions, where it enhances the transfer of anions from the aqueous phase to the organic phase. This compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in the production of various organic compounds. Additionally, it finds application in the preparation of ylides, which are crucial in Wittig reactions for forming alkenes. Its role in promoting efficient and selective reactions makes it a valuable tool in both academic research and industrial chemistry.
Product Specification:
Test Specification
Loss On Drying (%) 0-1
Melting Point (Degree Celsius) 164-169
Purity (Titration With AgNO3) (%) 94.5-105.5
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days $12.04
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25.000 10-20 days $26.99
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100.000 10-20 days $100.50
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Ethyltriphenylphosphonium iodide
Ethyltriphenylphosphonium iodide is widely used as a phase-transfer catalyst in organic synthesis, facilitating reactions between compounds in different phases. It is particularly effective in nucleophilic substitution reactions, where it enhances the transfer of anions from the aqueous phase to the organic phase. This compound is also employed in the synthesis of phosphonium salts, which are valuable intermediates in the production of various organic compounds. Additionally, it finds application in the preparation of ylides, which are crucial in Wittig reactions for forming alkenes. Its role in promoting efficient and selective reactions makes it a valuable tool in both academic research and industrial chemistry.
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