Diethylbenzenes
Chemical compound
From Wikipedia, the free encyclopedia
Diethylbenzene (DEB) is any of three isomers with the formula C6H4(C2H5)2. Each consists of a benzene ring and two ethyl substituents. The meta and para have the greater commercial significance. All are colorless solids.[1]
| Compound names | m.p. °C | b.p. °C | Density g/cm3 | Refractive Index |
|---|---|---|---|---|
| 1,2-Diethylbenzene, o-diethylbenzene | 31.2 | 183.5 | 0.8800 | 1.5035 |
| 1,3-Diethylbenzene, m-diethylbenzene | 83.9 | 181.1 | 0.8602 | 1.4955 |
| 1,4-Diethylbenzene, p-diethylbenzene | 42.8 | 183.8 | 0.8620 | 1.4967 |
The three isomers of diethylbenzene: ortho-, meta-, and para-diethylbenzene (left to right) | |
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3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.042.599 |
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PubChem CID |
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| UNII |
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| UN number | 2049 |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H14 | |
| Molar mass | 134.22 |
| Density | 0.87 g/mL |
| Hazards | |
| Flash point | 134.6 °F / 57 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Production and applications
Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can be described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene.
- C6H6 + C2H4 → C6H5C2H5
The diethylbenzene is an inadvertent side product.
- C6H5C2H5 + C2H4 → C6H4(C2H5)2
Using shape-selective zeolite catalysts, the para isomer can be produced in high selectivity.
Much diethylbenzene is recycled by transalkylation to give ethylbenzene:[1]
- C6H4(C2H5)2 + C6H6 → 2 C6H5C2H5
Uses
Diethylbenzene is used in a mixture with methyl and/or ethyl biphenyls as a low temperature heat transfer fluid.[2]
Diethylbenzene is dehydrogenated to give divinylbenzene (DVB):
- C6H4(C2H5)2 → C6H4(C2H3)2 + 2 H2
DVB is used in the production of crosslinked polystyrene.[3]
