Iodoethane, 98+%, stab. with copper, Thermo Scientific Chemicals
Iodoethane, 98+%, stab. with copper, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Iodoethane, 98+%, stab. with copper, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
100 g
500 g
2500 g
Catalog number A14444.22
also known as A14444-22
Price (USD)/ Each
40.65
Online exclusive
44.80 
Save 4.15 (9%)
-
Add to cart
Quantity:
100 g
Request bulk or custom format
Price (USD)/ Each
40.65
Online exclusive
44.80 
Save 4.15 (9%)
Add to cart
Iodoethane, 98+%, stab. with copper, Thermo Scientific Chemicals
Catalog numberA14444.22
Price (USD)/ Each
40.65
Online exclusive
44.80 
Save 4.15 (9%)
-
Add to cart
Chemical Identifiers
CAS75-03-6
IUPAC Nameiodoethane
Molecular FormulaC2H5I
InChI KeyHVTICUPFWKNHNG-UHFFFAOYSA-N
SMILESCCI
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
FormLiquid
Assay (GC)≥98.0%
Refractive Index1.5100-1.5140 @ 20?C
Iodoethane is an excellent ethylating agent used in organic synthesis to introduce an ethyl group into a compound. It reacts with magnesium to form the Grignard reagent, ethylmagnesium iodide which is used in organic synthesis. It is involved in the preparation of 1-ethyl-3-nitro-2-phenyl-indole and also serves as hydrogen radical promoter.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Iodoethane is an excellent ethylating agent used in organic synthesis to introduce an ethyl group into a compound. It reacts with magnesium to form the Grignard reagent, ethylmagnesium iodide which is used in organic synthesis. It is involved in the preparation of 1-ethyl-3-nitro-2-phenyl-indole and also serves as hydrogen radical promoter.

Solubility
Miscible with water.

Notes
Moisture and light sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong bases, strong oxidizing agents and magnesium.
RUO – Research Use Only

General References:

  1. Nijamudheen, A.; Datta, A. Mechanism for C-I Bond Dissociation in Iodoethane, Iodobenzene, and Iodoethene for the C-C Cross Coupling Reactions over Gold Clusters. J. Phys. Chem. C 2013, 117 (41), 21433-21440.
  2. Ljubic, I.; Matasovic, B.; Bonifacic, M. An efficient buffer-mediated control between free radical substitution and proton-coupled electron transfer: dehalogenation of iodoethane by the alpha-hydroxyethyl radical in aqueous solution. Phys. Chem. Chem. Phys. 2013, 15 (41), 18001-18011.