![]() | |
Names | |
---|---|
IUPAC name
Triethylindium
| |
Other names
Indium triethyl, triethylindigane, indiumtriethyl, TEI, TEIn
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.011.905 |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H15In | |
Molar mass | 202.004 g·mol−1 |
Appearance | Colorless liquid |
Boiling point | 144 °C (291 °F; 417 K) |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H250, H314 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Triethylindium is an
organometallic compound. Its chemical formula is C
6H
15In.
[1]
[2]
This compound can be obtained by reacting indium(III) bromide with a diethyl ether solution of Ethylmagnesium bromide:
Other routes are also known. [3]
Indium triethyl is a colorless, toxic, oxidation and hydrolysis-sensitive liquid. It is a monomer in the gaseous and dissolved state. The compound reacts with halomethanes to form diethyl indium halides. [4]
Triethylindium is highly reactive with water:
Indium triethyl is used to prepare indium phosphide layers for microelectronics. [5]
![]() | |
Names | |
---|---|
IUPAC name
Triethylindium
| |
Other names
Indium triethyl, triethylindigane, indiumtriethyl, TEI, TEIn
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.011.905 |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H15In | |
Molar mass | 202.004 g·mol−1 |
Appearance | Colorless liquid |
Boiling point | 144 °C (291 °F; 417 K) |
Hazards | |
GHS labelling: | |
![]() ![]() | |
Danger | |
H250, H314 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Triethylindium is an
organometallic compound. Its chemical formula is C
6H
15In.
[1]
[2]
This compound can be obtained by reacting indium(III) bromide with a diethyl ether solution of Ethylmagnesium bromide:
Other routes are also known. [3]
Indium triethyl is a colorless, toxic, oxidation and hydrolysis-sensitive liquid. It is a monomer in the gaseous and dissolved state. The compound reacts with halomethanes to form diethyl indium halides. [4]
Triethylindium is highly reactive with water:
Indium triethyl is used to prepare indium phosphide layers for microelectronics. [5]