Deuterated acetone

Deuterated acetone ((CD3)2CO), also known as Acetone-D6, is a form (called an isotopologue) of acetone (CH3)2CO in which the hydrogen atom ("H") is replaced with deuterium (heavy hydrogen) isotope ("D"). Deuterated acetone is a common solvent used in NMR spectroscopy.

Deuterated acetone
Skeletal formula of deuterated acetone
Spacefill model of deuterated acetone
Identifiers
3D model (JSmol)
1702935
ChEBI
ChemSpider
ECHA InfoCard 100.010.514
EC Number
  • 211-563-9
UNII
UN number 1090
Properties
C32H6O
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 pictograms
GHS Signal word Danger
GHS hazard statements
 H225, H319, H336
P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P303+361+353, P304+340, P305+351+338, P312, P337+313, P370+378, P403+233, P403+235, P405, P501
NFPA 704 (fire diamond)
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasolineHealth code 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3
1
0
Flash point −19 °C (−2 °F; 254 K)
Related compounds
Related compounds
 Acetone
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Properties

As with all deuterated compounds, the properties of deuterated acetone are virtually identical to those of regular acetone.

Manufacture

Deuterated acetone is prepared from heavy water, D2O, by what amounts to an aldol reaction. In this case, the base used is a deuterated version of lithium hydroxide:[1]

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.

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References
  1. P. J. Paulsen, W. D. Cooke. . Anal. Chem., 1963, 35 (10), pp 1560–1560. DOI: 10.1021/ac60203a072


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