Ethyltriphenylphosphonium iodide

95%

Reagent Code: #121964
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Alias Ethyltriphenylphosphine iodide
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CAS Number 4736-60-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 418.25 g/mol
Formula C₂₀H₂₀IP
badge Registry Numbers
EC Number 225-245-2
MDL Number MFCD00040352
inventory_2 Storage & Handling
Storage room temperature, away from light

description 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.

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Test Parameter Specification
Loss on Drying (%) 0-1%
Melting Point (°C) 164-169
Purity (Titration With AgNO3) (%) 94.5-105.5
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿2,420.00
inventory 25g
10-20 days ฿650.00
inventory 5g
10-20 days ฿290.00
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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