3-Pentanone, 2,4-dimethyl-

• Formula: C₇H₁₄O
• Molecular weight: 114.1855
• IUPAC Standard InChI: InChI=1S/C7H14O/c1-5(2)7(8)6(3)4/h5-6H,1-4H3 Copy

  
• IUPAC Standard InChIKey: HXVNBWAKAOHACI-UHFFFAOYSA-N Copy
• CAS Registry Number: 565-80-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Diisopropyl ketone; Isobutyrone; Isopropyl ketone; 2,4-Dimethyl-3-pentanone; 2,4-Dimethylpentan-3-one; (iso-C3H7)2CO; 2,4-dimethyl-3-pentanone (diisopropyl ketone)
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

Go To: Top, Normal boiling point, Notes

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

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Wright, 1961
Wright, F.J., Influence of temperature on viscosity of nonassociated liquids, J. Chem. Eng. Data, 1961, 6, 454. [all data]

Wright, 1960
Wright, F.J., Latent Heat of Vaporization and Composition, Recl. Trav. Chim. Pays-Bas, 1960, 79, 784-9. [all data]

Bartlett and Stiles, 1955
Bartlett, P.D.; Stiles, M., Highly branched molecules: IV solvolysis of the p-nitrobenzoate of tri-t- butylcarbinol and some of its homologs, J. Am. Chem. Soc., 1955, 77, 2806. [all data]

Cook, 1952
Cook, N.C., , Unpublished, Final Rep. Stand. Proj. on Oxygenated Compounds, Penn. State Univ., College Park, PA, 1952. [all data]

Herzog and Buchman, 1951
Herzog; Buchman, J. Org. Chem., 1951, 16, 99. [all data]

Swain and Boyles, 1951
Swain; Boyles, J. Am. Chem. Soc., 1951, 73, 870. [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]

Dreisbach and Martin, 1949
Dreisbach, R.R.; Martin, R.A., Physical Data on Some Organic Compounds, Ind. Eng. Chem., 1949, 41, 2875-8. [all data]

Howard, Mears, et al., 1947
Howard, F.L.; Mears, T.W.; Fookson, A.; Pomerantz, P.; Brooks, D.B., Preparation and physical properties of several aliphatic hydrocarbons and intermediates, J. Res. Natl. Bur. Stand. (U. S.), 1947, 38, 365. [all data]

Coley and Komarewsky, 1946
Coley, J.R.; Komarewsky, V.I., Catalytic conversion of aldols over chromia catalysts, J. Am. Chem. Soc., 1946, 68, 716. [all data]

Erickson and Kitchens, 1946
Erickson; Kitchens, J. Am. Chem. Soc., 1946, 68, 492. [all data]

Schallamach, 1946
Schallamach, Nature (London), 1946, 158, 619. [all data]

Ipatieff and Haensel, 1942
Ipatieff, V.N.; Haensel, V., J. Org. Chem., 1942, 7, 189. [all data]

Saylor, Baxt, et al., 1942
Saylor, J.H.; Baxt, V.J.; Gross, P.M., Solubility studies: vii the solubilities of some isomeric ketones in water, J. Am. Chem. Soc., 1942, 64, 2742-4. [all data]

Ewell and Welch, 1941
Ewell, R.H.; Welch, L.M., Maximum Boiling Mixtures of chloroparaffins with Donor Liquids, J. Am. Chem. Soc., 1941, 63, 2475. [all data]

Hudson and Hauser, 1941
Hudson, B.E.; Hauser, J. Am. Chem. Soc., 1941, 63, 3163. [all data]

Ginnings, Plonk, et al., 1940
Ginnings, P.M.; Plonk, D.; Carter, E., Aqueous Solubilities of Some Aliphatic Ketones, J. Am. Chem. Soc., 1940, 62, 1923-1924. [all data]

Hauser and Renfrow, 1937
Hauser; Renfrow, J. Am. Chem. Soc., 1937, 59, 1823. [all data]

Suknevich and Chilingaryan, 1936
Suknevich; Chilingaryan, Chem. Ber., 1936, 69, 1537. [all data]

Bryant and Smith, 1935
Bryant, M.D.; Smith, D.M., Improved hydroxylamine method for the determination of aldehydes and ketones displacement of oxime equilibria by means of pyridine, J. Am. Chem. Soc., 1935, 57, 57. [all data]

Bruzau, 1934
Bruzau, Ann. Chim. (Paris), 1934, 1, 257. [all data]

Kohlraush and Koppl, 1934
Kohlraush, K.W.F.; Koppl, F., Z. Phys. Chem., Abt. B, 1934, 24, 370. [all data]

Mayberry and Aston, 1934
Mayberry, M.G.; Aston, J.G., Vapor pressure of certain ketones., J. Am. Chem. Soc., 1934, 56, 2682-3. [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]

Terent'ev, 1925
Terent'ev, A., Bull. Soc. Chim. Fr., 1925, 37, 1553. [all data]

Murat and Amouroux, 1914
Murat, M.; Amouroux, G., Bull. Soc. Chim. Fr., 1914, 15, 159. [all data]

Sabatier and Mailhe, 1914
Sabatier, P.; Mailhe, A., C. R. Hebd. Seances Acad. Sci., 1914, 158, 830. [all data]

Favorskii, 1913
Favorskii, A., J. Prakt. Chem., 1913, 88, 641. [all data]

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

Haller and Bauer, 1910
Haller; Bauer, C. R. Hebd. Seances Acad. Sci., 1910, 150, 661. [all data]

Mailhe, 1909
Mailhe, A., Bull. Soc. Chim. Fr., 1909, 5, 616. [all data]

Senderens, 1909
Senderens, J.B., C. R. Hebd. Seances Acad. Sci., 1909, 148, 927. [all data]

Munch, 1876
Munch, R., Justus Liebigs Ann. Chem., 1876, 180, 327. [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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