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Ethyltriphenylphosphonium iodide

Basic information Safety Supplier Related

Ethyltriphenylphosphonium iodide Basic information

Product Name:
Ethyltriphenylphosphonium iodide
Synonyms:
  • Phosphonium, ethyltriphenyl-, iodide (1:1)
  • EPJ
  • ETPPI
  • ETHYLTRIPHENYLPHOSPHONIUM IODIDE
  • ETHYLTRIPHENYLPHOSPHONIUM IODIDE 99+%
  • Ethyltriphenylphosphonium iodide, 95 %
  • ETHYLTRIPHENYHLPHOSPHONIUM IODIDE
  • ETPPI: Ethyltriphenylphosphonium Iodide
CAS:
4736-60-1
MF:
C20H20IP
MW:
418.251031
EINECS:
225-245-2
Product Categories:
  • Pharmaceutical Intermediates
  • Phosphonium Compounds
  • Synthetic Organic Chemistry
  • Wittig & Horner-Emmons Reaction
  • Wittig Reaction
  • Greener Alternatives: Catalysis
  • C-C Bond Formation
  • Olefination
  • Wittig Reagents
  • Phase Transfer Catalysts
  • Phosphonium SaltsC-C Bond Formation
Mol File:
4736-60-1.mol
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Ethyltriphenylphosphonium iodide Chemical Properties

Melting point:
164-168 °C(lit.)
Boiling point:
337 °C
Density 
1.500
vapor pressure 
0Pa at 25℃
Flash point:
226 °C
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Acetone, Chloroform, Dichloromethane, Methanol
form 
Powder
color 
Yellow
Water Solubility 
slightly soluble
Sensitive 
Light Sensitive & Hygroscopic
BRN 
3659323
InChIKey
SLAFUPJSGFVWPP-UHFFFAOYSA-M
LogP
0.324
CAS DataBase Reference
4736-60-1(CAS DataBase Reference)
EPA Substance Registry System
Phosphonium, ethyltriphenyl-, iodide (4736-60-1)
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Safety Information

Hazard Codes 
T,Xn
Risk Statements 
25-36/38-21-36/37/38-20/21/22
Safety Statements 
45-36/37/39-28A-26-36
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
TA2312000
3-8-10
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29310095

MSDS

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Ethyltriphenylphosphonium iodide Usage And Synthesis

Chemical Properties

Ethyltriphenylphosphonium iodide is white to slightly yellowish crystalline powder

Uses

Ethyltriphenylphosphonium iodide is used as a Wittig reagent and phase transfer catalyst in organic synthesis. It can also be used in asymmetric hydrogenation and to make Bismuth(III) polynuclear complexes.

Uses

Ethyltriphenylphosphonium iodide is involved in synthesis of diarylmethine derivatives, phosphonium salts, and bismuth(III) polynuclear halide complexes, asymmetric hydrogenation.

Flammability and Explosibility

Not classified

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