tert-Butylbenzene
Appearance
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Names | |
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Preferred IUPAC name
tert-Butylbenzene | |
Other names
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Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.002.394 |
EC Number |
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PubChem CID
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UNII | |
UN number | 2709 |
CompTox Dashboard (EPA)
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Properties | |
C10H14 | |
Molar mass | 134.22 |
Appearance | colorless liquid |
Density | 0.867 g/cm3 |
Melting point | −57.9 °C (−72.2 °F; 215.2 K) |
Boiling point | 169 °C (336 °F; 442 K) |
insoluble | |
Solubility in organic solvents | miscible |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Flammable |
GHS labelling: | |
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Warning | |
H226, H315, H319 | |
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P312, P321, P332+P313, P362, P370+P378, P403+P235, P501 | |
Flash point | 34.4 °C (93.9 °F; 307.5 K) |
450 °C (842 °F; 723 K) | |
Related compounds | |
Related compounds
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iso-Butylbenzene, sec-Butylbenzene, n-Butylbenzene |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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tert-Butylbenzene is an organic compound classified as an aromatic hydrocarbon. Its structure consists of a benzene ring substituted with a tert-butyl group. It is a flammable colorless liquid which is nearly insoluble in water but miscible with organic solvents.
Production
[edit]tert-Butylbenzene can be produced by the treatment of benzene with isobutene[1] or by the reaction of benzene with tert-butyl chloride in presence of anhydrous aluminium chloride,[2] the latter is depicted below:
![](http://178.128.105.246/cars-http-upload.wikimedia.org/wikipedia/commons/thumb/5/50/Tert-Butylbenzene_synthesis.png/500px-Tert-Butylbenzene_synthesis.png)
References
[edit]- ^ Griesbaum, Karl; Behr, Arno; Biedenkapp, Dieter; Voges, Heinz-Werner; Garbe, Dorothea; Paetz, Christian; Collin, Gerd; Mayer, Dieter; Höke, Hartmut (2002). "Hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a13_227. ISBN 978-3527306732.
- ^ Fieser, Louis F. (1941), Experiments in Organic Chemistry, Second Edition, pp. 180–181, doi:10.1021/ed018p550.1