Deuterated benzene
| |||
| |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name
(2H6)Benzene[1] | |||
| Identifiers | |||
3D model (JSmol)
|
|||
| 1905426 | |||
| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.012.784 | ||
| EC Number |
| ||
PubChem CID
|
|||
| UN number | 1114 | ||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
| Properties | |||
| C62H6 | |||
| Molar mass | 84.1488 g mol−1 | ||
| Density | 0.950 g cm−3 | ||
| Melting point | 7 °C; 44 °F; 280 K | ||
| Boiling point | 79 °C; 174 °F; 352 K | ||
| Thermochemistry | |||
Heat capacity (C)
|
152.46 J K−1 mol−1 | ||
| Hazards | |||
| GHS labelling: | |||
  
| |||
| Danger | |||
| H225, H304, H315, H319, H340, H350, H372 | |||
| P201, P202, P210, P233, P240, P241, P242, P243, P260, P264, P270, P280, P281, P301+P310, P302+P352, P303+P361+P353, P305+P351+P338, P308+P313, P314, P321, P331, P332+P313, P337+P313, P362, P370+P378, P403+P235, P405, P501 | |||
| NFPA 704 (fire diamond) | |||
| Flash point | −11 °C (12 °F; 262 K) | ||
| Related compounds | |||
Related compounds
|
Benzene | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |||
Deuterated benzene (C6D6) is an isotopologue of benzene (C6H6) in which the hydrogen atom ("H") is replaced with deuterium (heavy hydrogen) isotope ("D").
Properties
The properties of deuterated benzene are very similar to those of normal benzene, however, the increased atomic weight of deuterium relative to protium means that the melting point of C6D6 is about 1.3 °C higher than that of the nondeuterated analogue. The boiling points of both compounds, however, are the same: 80 °C.[2]
Applications
Deuterated benzene is a common solvent used in NMR spectroscopy. It is widely used for taking spectra of organometallic compounds, which often react with the cheaper deuterated chloroform.[3]
A slightly more exotic application of C6D6 is in the synthesis of molecules containing a deuterated phenyl group. Deuterated benzene will undergo all the same reactions its normal analogue will, just a little more slowly due to the kinetic isotope effect. For example, deuterated benzene could be used in the synthesis of deuterated benzoic acid, if desired:
Many simple monosubstituted aromatic compounds bearing the deuterated phenyl (C6D5) group may be purchased commercially, such as aniline, acetophenone, nitrobenzene, bromobenzene, and more.
References
- ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 1142. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ^ "Benzene-d6". sigmaaldrich.com. Retrieved 4 August 2023.
- ^ Fulmer, Gregory R.; Miller, Alexander J. M.; Sherden, Nathaniel H.; Gottlieb, Hugo E.; Nudelman, Abraham; Stoltz, Brian M.; Bercaw, John E.; Goldberg, Karen I. (2010). "NMR Chemical Shifts of Trace Impurities: Common Laboratory Solvents, Organics, and Gases in Deuterated Solvents Relevant to the Organometallic Chemist" (PDF). Organometallics. 29 (9): 2176–2179. doi:10.1021/om100106e.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |