2-Heptanone

• Formula: C₇H₁₄O
• Molecular weight: 114.1855
• IUPAC Standard InChI: InChI=1S/C7H14O/c1-3-4-5-6-7(2)8/h3-6H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: CATSNJVOTSVZJV-UHFFFAOYSA-N Copy
• CAS Registry Number: 110-43-0
• 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: n-Amyl methyl ketone; n-Pentyl methyl ketone; Amyl methyl ketone; Butylacetone; Heptan-2-one; Methyl amyl ketone; Methyl n-amyl ketone; Methyl n-pentyl ketone; Methyl pentyl ketone; Pentyl methyl ketone; n-C5H11COCH3; 2-Ketoheptane; Amyl-methyl-cetone; Ketone, methyl pentyl; Methyl-amyl-cetone; UN 1110; Ketone C-7; 2-Heptanal; Heptanone-2; NSC 7313
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • 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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - 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.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

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]

Ivanskii and Dolgov, 1963
Ivanskii, V.I.; Dolgov, B.N., New Catalysts for Obtaining Tetrahydrofuran and γ-Butyrolactone from 1,4-Butanediol, Zh. Prikl. Khim. (Leningrad), 1963, 36, 2256. [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]

Shenton and Smith, 1958
Shenton, T.; Smith, J.C., Chem. Ind. (London), 1958, 1958, 1510. [all data]

Doolittle, 1954
Doolittle, A.K., The Technology of Solvents and Plasticizers, Wiley-Inter- science, New York, 1954. [all data]

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Cook, N.C., , Unpublished, Final Rep.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

Pomerantz, 1952
Pomerantz, P., Synthesis and physical properties of n-heptane and 2,2,4-trimethylpentane, J. Res. Natl. Bur. Stand. (U. S.), 1952, 48, 76-81. [all data]

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

Patton, 1950
Patton, S., J. Dairy Sci., 1950, 33, 680. [all data]

Othmer and Benenati, 1945
Othmer, D.F.; Benenati, R.F., Composition of vapors from boiling binary solutions: aqueous systems of acetone, methanol, and methyl ethyl ketone; and other systems with acetic acid as one component, Ind. Eng. Chem., 1945, 37, 299-303. [all data]

Platt, Rusoff, et al., 1943
Platt, J.R.; Rusoff, I.I.; Klevens, H.B., J. Chem. Phys., 1943, 11, 535. [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]

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]

Stuckey and Saylor, 1940
Stuckey, J.M.; Saylor, J.H., Vapor Pressures of Organic Compounds I., J. Am. Chem. Soc., 1940, 62, 2922. [all data]

Thomas, Campbell, et al., 1938
Thomas, R.J.; Campbell, K.N.; Hennion, G.F., Catalytic Hydration of Alkylacetylenes, J. Am. Chem. Soc., 1938, 60, 718-20. [all data]

Slanina and Hennion, 1937
Slanina, S.J.; Hennion, G.F., Reactions of Alkenyl Esters Derived from Alkylacetylenes, J. Am. Chem. Soc., 1937, 59, 855. [all data]

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

Sprague and Adkins, 1934
Sprague, J.M.; Adkins, H., Hydrogenation and Hydrogenolysis of 1,3-Diketones., J. Am. Chem. Soc., 1934, 56, 2669. [all data]

Whitmore and Williams, 1933
Whitmore, F.C.; Williams, F.E., Aliphatic tertiary alcohols and chlorides containing the normal amyl group and the related olefins and their ozonolysis, J. Am. Chem. Soc., 1933, 55, 406. [all data]

Mathews and Fehlandt, 1931
Mathews, J.H.; Fehlandt, P.R., The Heats of Vaporization of Some Organic Compounds, J. Am. Chem. Soc., 1931, 53, 3212. [all data]

Simon, 1929
Simon, I., Freezing Temperature of Organic Compounds. XI. Compounds in C5 and C6., Bull. Soc. Chim. Belg., 1929, 38, 47-70. [all data]

Suida and Poll, 1927
Suida, H.; Poll, Angew. Chem., 1927, 40, 505. [all data]

Tsumuri, 1927
Tsumuri, S., Sci. Rep. Tohoku Imp. Univ., Ser. 1, 1927, 16, 677. [all data]

Weizmann and Garrard, 1920
Weizmann, C.; Garrard, J. Chem. Soc., 1920, 117, 324. [all data]

Michael, 1919
Michael, A., J. Am. Chem. Soc., 1919, 41, 393. [all data]

Pickard and Kenyon, 1911
Pickard, R.H.; Kenyon, J., J. Chem. Soc., 1911, 99, 45. [all data]

Masson, 1909
Masson, H., C. R. Hebd. Seances Acad. Sci., 1909, 149, 630. [all data]

Schorlemmer, 1873
Schorlemmer, C., Justus Liebigs Ann. Chem., 1873, 161, 263. [all data]

Popoff, 1865
Popoff, Z. Chem., 1865, 8, 577. [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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