| |
| Names | |
|---|---|
|
IUPAC name
Ethaneperoxol
| |
| Other names
Hydroperoxide, ethyl
Ethane hydroperoxide Ethyl hydrogen peroxide Hydroperoxyethane | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
| ECHA InfoCard | 100.019.284 |
| EC Number |
|
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C2H6O2 | |
| Molar mass | 62.068 g·mol−1 |
| Appearance | colorless liquid |
| Melting point | −100 °C (−148 °F; 173 K) |
| Boiling point | 95 °C (203 °F; 368 K) |
| Miscible in water and diethyl ether | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Ethyl hydroperoxide is the organic compound with the formula CH3CH2OOH. It is a colorless liquid that is miscible with water and diethyl ether.
Formation
Ethyl hydroperoxide is formed in the flame of burning alkanes. [1] Ethyl hydroperoxide is also formed in the catalytic reaction of ethane and hydrogen peroxide. [2] Yet another way to form ethyl hydroperoxide is by a photocatalytic oxidation of ethane: [3]
- CH3CH3 + O2 → CH3CH2OOH
References
- ^ Bierkandt, Thomas; Oßwald, Patrick; Gaiser, Nina; Krüger, Dominik; Köhler, Markus; Hoener, Martin; Shaqiri, Shkelqim; Kaczmarek, Dennis; Karakaya, Yasin; Hemberger, Patrick; Kasper, Tina (October 2021). "Observation of low‐temperature chemistry products in laminar premixed low‐pressure flames by molecular‐beam mass spectrometry". International Journal of Chemical Kinetics. 53 (10): 1063–1081. doi: 10.1002/kin.21503. S2CID 236545874.
- ^ Forde, Michael M.; Armstrong, Robert D.; Hammond, Ceri; He, Qian; Jenkins, Robert L.; Kondrat, Simon A.; Dimitratos, Nikolaos; Lopez-Sanchez, Jose Antonio; Taylor, Stuart H.; Willock, David; Kiely, Christopher J.; Hutchings, Graham John (31 July 2013). "Partial Oxidation of Ethane to Oxygenates Using Fe- and Cu-Containing ZSM-5". Journal of the American Chemical Society. 135 (30): 11087–11099. doi: 10.1021/ja403060n. PMID 23802759.
- ^ Zhu, Yao; Fang, Siyuan; Chen, Shaoqin; Tong, Youjie; Wang, Chunling; Hu, Yun Hang (2021). "Highly efficient visible-light photocatalytic ethane oxidation into ethyl hydroperoxide as a radical reservoir". Chemical Science. 12 (16): 5825–5833. doi: 10.1039/D1SC00694K. PMC 8179680. PMID 34168807.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
IUPAC name
Ethaneperoxol
| |
| Other names
Hydroperoxide, ethyl
Ethane hydroperoxide Ethyl hydrogen peroxide Hydroperoxyethane | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
| ECHA InfoCard | 100.019.284 |
| EC Number |
|
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C2H6O2 | |
| Molar mass | 62.068 g·mol−1 |
| Appearance | colorless liquid |
| Melting point | −100 °C (−148 °F; 173 K) |
| Boiling point | 95 °C (203 °F; 368 K) |
| Miscible in water and diethyl ether | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Ethyl hydroperoxide is the organic compound with the formula CH3CH2OOH. It is a colorless liquid that is miscible with water and diethyl ether.
Formation
Ethyl hydroperoxide is formed in the flame of burning alkanes. [1] Ethyl hydroperoxide is also formed in the catalytic reaction of ethane and hydrogen peroxide. [2] Yet another way to form ethyl hydroperoxide is by a photocatalytic oxidation of ethane: [3]
- CH3CH3 + O2 → CH3CH2OOH
References
- ^ Bierkandt, Thomas; Oßwald, Patrick; Gaiser, Nina; Krüger, Dominik; Köhler, Markus; Hoener, Martin; Shaqiri, Shkelqim; Kaczmarek, Dennis; Karakaya, Yasin; Hemberger, Patrick; Kasper, Tina (October 2021). "Observation of low‐temperature chemistry products in laminar premixed low‐pressure flames by molecular‐beam mass spectrometry". International Journal of Chemical Kinetics. 53 (10): 1063–1081. doi: 10.1002/kin.21503. S2CID 236545874.
- ^ Forde, Michael M.; Armstrong, Robert D.; Hammond, Ceri; He, Qian; Jenkins, Robert L.; Kondrat, Simon A.; Dimitratos, Nikolaos; Lopez-Sanchez, Jose Antonio; Taylor, Stuart H.; Willock, David; Kiely, Christopher J.; Hutchings, Graham John (31 July 2013). "Partial Oxidation of Ethane to Oxygenates Using Fe- and Cu-Containing ZSM-5". Journal of the American Chemical Society. 135 (30): 11087–11099. doi: 10.1021/ja403060n. PMID 23802759.
- ^ Zhu, Yao; Fang, Siyuan; Chen, Shaoqin; Tong, Youjie; Wang, Chunling; Hu, Yun Hang (2021). "Highly efficient visible-light photocatalytic ethane oxidation into ethyl hydroperoxide as a radical reservoir". Chemical Science. 12 (16): 5825–5833. doi: 10.1039/D1SC00694K. PMC 8179680. PMID 34168807.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |