3-Pentanone, 2,2-dimethyl-

• Formula: C₇H₁₄O
• Molecular weight: 114.1855
• IUPAC Standard InChI: InChI=1S/C7H14O/c1-5-6(8)7(2,3)4/h5H2,1-4H3 Copy

  
• IUPAC Standard InChIKey: VLNUTKMHYLQCQB-UHFFFAOYSA-N Copy
• CAS Registry Number: 564-04-5
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: tert-Butyl Ethyl ketone; Ethyl tert-butyl ketone; 2,2-Dimethyl-3-pentanone
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal boiling point

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Foley, Welch, et al., 1959
Foley, W.M.; Welch, F.J.; La Combe, E.; Mosher, H.S., Asymmetric reductions: vi the action of the grignard reagent from (+)-1- chloro-2-methylbutane on a series of alkyl t-butyl ketones, J. Am. Chem. Soc., 1959, 81, 2779. [all data]

Mosher, Cox, et al., 1953
Mosher, W.A.; Cox, J.C.; Kreitzer, J., 2,2-dimethyl-3-aminopentane and its reaction with nitrosyl chloride, J. Am. Chem. Soc., 1953, 75, 4605. [all data]

Mosher and Mooney, 1951
Mosher; Mooney, J. Am. Chem. Soc., 1951, 73, 3948. [all data]

Hauser and Humphlett, 1950
Hauser, C.R.; Humphlett, W.J., J. Org. Chem., 1950, 15, 359. [all data]

Miller, Cook, et al., 1950
Miller, A.L.; Cook, N.C.; Whitmore, F.C., The Ketonic Decarboxylation Reaction: The Ketonic Decarboxylation of Trimethylacetic Acid and Isobutyric Acid, J. Am. Chem. Soc., 1950, 72, 2732. [all data]

Pomerantz, Mears, et al., 1949
Pomerantz, P.; Mears, T.W.; Howard, F.L., Separation and Identification of the Major C1 to C10 Components of Triptene Residue, J. Res. Natl. Bur. Stand. (U. S.), 1949, 42, 617-32. [all data]

Whitmore and Block, 1942
Whitmore, F.C.; Block, L.P., Grignard Reactions XV. Sterically Hindered Aliphatic Carbonyl Compounds V. Enolization Studies I, J. Am. Chem. Soc., 1942, 64, 1619. [all data]

Kharasch, Sternfeld, et al., 1940
Kharasch, M.S.; Sternfeld, E.; Mayo, F.R., J. Org. Chem., 1940, 5, 362. [all data]

Whitmore, Noll, et al., 1939
Whitmore, F.C.; Noll, C.I.; Meunier, V.C., J. Am. Chem. Soc., 1939, 61, 683. [all data]

Pfeiffer and Adkins, 1931
Pfeiffer, G.J.; Adkins, H., The Relation of the Structure of Ketones to Their Reactivity and Affinity in Acetal Formation II., J. Am. Chem. Soc., 1931, 53, 1043. [all data]

Haller and Bauer, 1913
Haller, A.; Bauer, E., Ann. Chim. (Paris), 1913, 29, 8, 313. [all data]

Haller and Bauer, 1910
Haller, A.; Bauer, A., C. R. Hebd. Seances Acad. Sci., 1910, 150, 582. [all data]

Wischnegradsky, 1875
Wischnegradsky, A., Justus Liebigs Ann. Chem., 1875, 178, 103. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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