Ethyl iodide

Ethyl iodide
Names
IUPAC name
Iodoethane[1]
Identifiers
75-03-6 YesY
3D model (Jmol) Interactive image
505934
ChEBI CHEBI:42487 N
ChEMBL ChEMBL1232588 N
ChemSpider 6100 YesY
ECHA InfoCard 100.000.758
EC Number 200-833-1
PubChem 6340
RTECS number KI4750000
Properties
C2H5I
Molar mass 155.97 g·mol−1
Appearance Colourless liquid
Density 1.940 g mL−1
Melting point −111.10 °C; −167.98 °F; 162.05 K
Boiling point 71.5 to 73.3 °C; 160.6 to 163.8 °F; 344.6 to 346.4 K
4 g L−1 (at 20 °C)
Solubility in ethanol Miscible
Solubility in diethyl ether Miscible
log P 2.119
Vapor pressure 17.7 kPa
1.8 μmol Pa−1 kg−1
1.513–1.514
Viscosity 5.925 mPa s (at 20 °C)
Thermochemistry
109.7 J K−1 mol−1
−39.9–−38.3 kJ mol−1
−1.4629–−1.4621 MJ mol−1
Hazards
GHS pictograms
GHS signal word DANGER
H302, H315, H317, H319, H334, H335
P261, P280, P305+351+338, P342+311
Xn
R-phrases R20, R36/37/38, R42/43
S-phrases S23, S26, S36/37, S45
NFPA 704
Flammability code 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g., canola oil Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g., calcium Special hazards (white): no codeNFPA 704 four-colored diamond
1
2
1
Flash point 72 °C (162 °F; 345 K)
Lethal dose or concentration (LD, LC):
330 g m−3 (oral, rat)
Related compounds
Related iodoalkanes
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Ethyl iodide (also iodoethane) is a colorless, flammable chemical compound. It has the chemical formula C2H5I and is prepared by heating ethanol with iodine and phosphorus.[2] On contact with air, especially on the effect of light, it decomposes and turns yellow or reddish from dissolved iodine. It may also be prepared by reaction between hydroiodic acid and ethanol distilling off the ethyl iodide. Ethyl iodide should be stored in copper powder to avoid fast decomposition, though even with this method samples don't last more than 1 year.

Ethyl iodide distillation. It has a greenish color due to decomposition.

Because iodide is a good leaving group, ethyl iodide is an excellent ethylating agent. It is also used as the hydrogen radical promoter.

Production

Ethyl iodide is prepared by using red phosphorus, absolute ethanol and iodine ; the phosphorus and iodine dissolve in the ethanol, where they form phosphorus triiodide, which must be formed in situ because it is unstable.[3] During the process the temperature is controlled.

The crude product is purified by distillation.

References

  1. ↑ "iodoethane - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 29 February 2012.
  2. ↑ Merck Index of Chemicals and Drugs, 9th ed., monograph 3753
  3. ↑ Csámpai,A;Láng,E;Majer,Zs;Orosz,Gy;Rábai,J;Ruff,F;Schlosser,G;Szabó,D;Vass,E: Szerves Kémiai Praktikum page: 274, Eötvös kiadó 2012 ISBN 978-963-312-129-0


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