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Names | |||
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Preferred IUPAC name
(1,1,1,3,3,3-2H6)Propan-2-one | |||
Identifiers | |||
3D model (JSmol)
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1702935 | |||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.010.514 | ||
EC Number |
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PubChem CID
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UNII | |||
UN number | 1090 | ||
CompTox Dashboard (EPA)
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Properties | |||
C32H6O or C3D6O | |||
Molar mass | 64.1161 g mol−1 | ||
Density | 0.872 g cm−3 | ||
Melting point | −94 °C (−137 °F; 179 K) | ||
Boiling point | 56 °C (133 °F; 329 K) | ||
Vapor pressure | 24.5-25.3 kPa (at 20°C) | ||
Hazards | |||
GHS labelling: | |||
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Danger | |||
H225, H319, H336 | |||
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P303+P361+P353, P304+P340, P305+P351+P338, P312, P337+P313, P370+P378, P403+P233, P403+P235, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | −19 °C (−2 °F; 254 K) | ||
Related compounds | |||
Related compounds
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Acetone | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Deuterated acetone ((CD3)2CO), also known as acetone-d6, is a form (isotopologue) of acetone (CH3)2CO in which the hydrogen atom (H) is replaced with deuterium (heavy hydrogen) isotope (2H or D). Deuterated acetone is a common solvent used in NMR spectroscopy.[1]
Properties
As with all deuterated compounds, the properties of deuterated acetone are virtually identical to those of regular acetone.
Manufacture
Deuterated acetone is prepared by the reaction of acetone with heavy water, 2H2O or D2O, in the presence of a base. In this case, the base used is deuterated lithium hydroxide:[1]
![](https://upload.wikimedia.org/wikipedia/commons/thumb/1/17/Deuteration_of_acetone.svg/750px-Deuteration_of_acetone.svg.png)
In order to fully deuterate the acetone, the process is repeated several times, distilling off the acetone from the heavy water, and re-running the reaction in a fresh batch of heavy water.
References
- ^ a b Paulsen, P. J.; Cooke, W. D. (1963). "Preparation of Deuterated Solvents for Nuclear Magnetic Resonance Spectrometry". Analytical Chemistry. 35 (10): 1560. doi:10.1021/ac60203a072.