2-Butanone, 3-methyl-
- Formula: C5H10O
- Molecular weight: 86.1323
- IUPAC Standard InChIKey: SYBYTAAJFKOIEJ-UHFFFAOYSA-N
- CAS Registry Number: 563-80-4
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Isopropyl methyl ketone; Ketone, isopropyl methyl; Methyl butanone-2; Methyl isopropyl ketone; 3-Methyl-2-butanone; iso-C3H7COCH3; 2-Acetylpropane; 3-Methylbutan-2-one; MIPK; UN 2397; 2-Methylbutan-3-one; NSC 9379; methylbutanone; 3-Methyl-2-butanoate; 3-methylbutanone
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Normal boiling point
Go To: Top, References, Notes
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
Tboil (K) | Reference | Comment |
---|---|---|
367.7 | Weast and Grasselli, 1989 | BS |
367.4 | Majer and Svoboda, 1985 | |
389.5 | Wisniak and Tamir, 1976 | Uncertainty assigned by TRC = 0.3 K; TRC; Data excluded from overall average |
368.3 | Grove and Walden, 1965 | Uncertainty assigned by TRC = 0.6 K; TRC |
368. | Grove and Walden, 1965 | Uncertainty assigned by TRC = 0.4 K; TRC |
366.65 | Fitzpatrick and Gettler, 1956 | Uncertainty assigned by TRC = 1. K; TRC |
367.15 | Hickinbottom, Peters, et al., 1955 | Uncertainty assigned by TRC = 1. K; TRC |
367.65 | Hickinbottom, Hyatt, et al., 1954 | Uncertainty assigned by TRC = 1. K; TRC |
367.35 | Cook, 1952 | Uncertainty assigned by TRC = 0.5 K; TRC |
367.65 | Bridson-Jones and Buckley, 1951 | Uncertainty assigned by TRC = 1. K; TRC |
367.9 | Elderfield and McCarthy, 1951 | Uncertainty assigned by TRC = 0.5 K; TRC |
366.15 | Lauchenauer and Schinz, 1951 | Uncertainty assigned by TRC = 2. K; TRC |
367.35 | Mears, Fookson, et al., 1950 | Uncertainty assigned by TRC = 0.5 K; TRC |
368.55 | Lecat, 1949 | Uncertainty assigned by TRC = 2. K; TRC |
365.65 | Pomerantz, Mears, et al., 1949 | Uncertainty assigned by TRC = 2. K; TRC |
368.6 | Lecat, 1947 | Uncertainty assigned by TRC = 0.5 K; TRC |
368.15 | Coley and Komarewsky, 1946 | Uncertainty assigned by TRC = 2. K; TRC |
366.7 | Ginnings, Plonk, et al., 1940 | Uncertainty assigned by TRC = 0.5 K; TRC |
367.41 | Rintelen, Saylor, et al., 1937 | Uncertainty assigned by TRC = 0.5 K; TRC |
365.15 | Ivanov and Spassov, 1935 | Uncertainty assigned by TRC = 5. K; TRC |
367.3 | Kohlraush and Koppl, 1934 | Uncertainty assigned by TRC = 1. K; TRC |
366.15 | Whitmore, Evers, et al., 1933 | Uncertainty assigned by TRC = 1. K; TRC |
366.65 | Bardan, 1931 | Uncertainty assigned by TRC = 2. K; TRC |
365.65 | Hopff, 1931 | Uncertainty assigned by TRC = 5. K; TRC |
366.65 | Suida and Poll, 1927 | Uncertainty assigned by TRC = 1. K; TRC |
366.65 | Daniloff and Venus-Danilova, 1926 | Uncertainty assigned by TRC = 1. K; TRC |
368.15 | Morgan and Drew, 1924 | Uncertainty assigned by TRC = 2. K; TRC |
365.15 | Pringsheim and Leibowitz, 1923 | Uncertainty assigned by TRC = 2. K; TRC |
366.65 | Mailhe, 1921 | Uncertainty assigned by TRC = 1. K; TRC |
368.65 | Timmermans and Mattaar, 1921 | Uncertainty assigned by TRC = 1. K; TRC |
367.65 | Michael, 1919 | Uncertainty assigned by TRC = 2. K; TRC |
368.3 | Clarke, 1911 | Uncertainty assigned by TRC = 2. K; TRC |
367.15 | Eisenlohr, 1910 | Uncertainty assigned by TRC = 1. K; TRC |
367.65 | Henry, 1907 | Uncertainty assigned by TRC = 2. K; TRC |
366.15 | Samec, 1907 | Uncertainty assigned by TRC = 1. K; TRC |
366.65 | Moureu and Delange, 1903 | Uncertainty assigned by TRC = 1. K; TRC |
365.55 | Louguinine, 1898 | Uncertainty assigned by TRC = 0.3 K; TRC |
367.65 | Behal, 1888 | Uncertainty assigned by TRC = 2. K; TRC |
366.65 | Winogradow, 1878 | Uncertainty assigned by TRC = 1. K; TRC |
366.65 | Munch, 1876 | Uncertainty assigned by TRC = 1. K; TRC |
366.65 | Frankland and Duppa, 1866 | Uncertainty assigned by TRC = 1. K; TRC |
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]
Majer and Svoboda, 1985
Majer, V.; Svoboda, V.,
Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]
Wisniak and Tamir, 1976
Wisniak, J.; Tamir, A.,
Association effects in propionic acid systems,
J. Chem. Eng. Data, 1976, 21, 88-90. [all data]
Grove and Walden, 1965
Grove, E.L.; Walden, G.E.,
Variation of Dielectric Constant with Temperature for SOme Five- and Six-Carbon Ketones,
J. Chem. Eng. Data, 1965, 10, 98. [all data]
Fitzpatrick and Gettler, 1956
Fitzpatrick, F.W.; Gettler, J.D.,
J. Am. Chem. Soc., 1956, 78, 530. [all data]
Hickinbottom, Peters, et al., 1955
Hickinbottom, W.J.; Peters, D.; Wood, D.G.M.,
J. Chem. Soc., 1955, 1955, 1360. [all data]
Hickinbottom, Hyatt, et al., 1954
Hickinbottom, W.J.; Hyatt, A.A.; Sparke, M.B.,
J. Chem. Soc., 1954, 1954, 2533. [all data]
Cook, 1952
Cook, N.C.,
, Unpublished, Final Rep. Stand. Proj. on Oxygenated Compounds, Penn. State Univ., College Park, PA, 1952. [all data]
Bridson-Jones and Buckley, 1951
Bridson-Jones, F.S.; Buckley, G.D.,
Oxidation of organic compounds by nitrous oxide: II tri- and tetra- substituted ethylenes,
J. Chem. Soc., 1951, 1951, 3009. [all data]
Elderfield and McCarthy, 1951
Elderfield, R.C.; McCarthy, J.R.,
The reaction of o-phenylenediamines with carbonyl compounds: II aliphatic ketones,
J. Am. Chem. Soc., 1951, 73, 975. [all data]
Lauchenauer and Schinz, 1951
Lauchenauer; Schinz,
Helv. Chim. Acta, 1951, 34, 1514. [all data]
Mears, Fookson, et al., 1950
Mears, T.W.; Fookson, A.; Pomerantz, P.; Rich, E.H.; Dussinger, C.S.; Howard, F.L.,
Syntheses and Properties of Two Olefins, Six Paraffins, and Their Intermediates,
J. Res. Natl. Bur. Stand. (U. S.), 1950, 44, 299. [all data]
Lecat, 1949
Lecat, M.,
Tables Azeotropiques, Vol. 1, 10th ed., Brussels, Belgium, 1949. [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]
Lecat, 1947
Lecat, M.,
Orthobaric Azeotropes of Sulfides,
Bull. Cl. Sci., Acad. R. Belg., 1947, 33, 160-82. [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]
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]
Rintelen, Saylor, et al., 1937
Rintelen, J.C.; Saylor, J.H.; Gross, P.M.,
The Densities and Vapor Pressures of Some Alkylbenzene, Aliphatic Ketones and n-AMyl Chloride,
J. Am. Chem. Soc., 1937, 59, 1129. [all data]
Ivanov and Spassov, 1935
Ivanov; Spassov,
Bull. Soc. Chim. Fr., 1935, 2, 816. [all data]
Kohlraush and Koppl, 1934
Kohlraush, K.W.F.; Koppl, F.,
Z. Phys. Chem., Abt. B, 1934, 24, 370. [all data]
Whitmore, Evers, et al., 1933
Whitmore, F.C.; Evers, W.L.; Rothrock, H.S.,
Org. Synth., 1933, 13, 68. [all data]
Bardan, 1931
Bardan, B.,
Bull. Soc. Chim. Fr., 1931, 49, 1875. [all data]
Hopff, 1931
Hopff, H.,
Chem. Ber., 1931, 64, 2739. [all data]
Suida and Poll, 1927
Suida, H.; Poll,
Angew. Chem., 1927, 40, 505. [all data]
Daniloff and Venus-Danilova, 1926
Daniloff, S.; Venus-Danilova, E.D.,
The isomerization of aldehydes to ketones and its connection with the dehydration of alpha-secondary-tertiary hydrobenzoin + glycols,
Ber. Dtsch. Chem. Ges., 1926, 59, 377. [all data]
Morgan and Drew, 1924
Morgan; Drew,
J. Chem. Soc., 1924, 125, 731. [all data]
Pringsheim and Leibowitz, 1923
Pringsheim; Leibowitz,
Chem. Ber., 1923, 56, 2034. [all data]
Mailhe, 1921
Mailhe, A.,
Bull. Soc. Chim. Fr., 1921, 29, 219. [all data]
Timmermans and Mattaar, 1921
Timmermans, J.; Mattaar, J.F.,
Freezing points of orgainic substances VI. New experimental determinations.,
Bull. Soc. Chim. Belg., 1921, 30, 213. [all data]
Michael, 1919
Michael, A.,
J. Am. Chem. Soc., 1919, 41, 393. [all data]
Clarke, 1911
Clarke, L.,
2,3-dimethylhexane,
J. Am. Chem. Soc., 1911, 33, 520. [all data]
Eisenlohr, 1910
Eisenlohr, F.,
Z. Phys. Chem. (Leipzig), 1910, 75, 585. [all data]
Henry, 1907
Henry, L.,
C. R. Hebd. Seances Acad. Sci., 1907, 145, 21. [all data]
Samec, 1907
Samec, M.,
Justus Liebigs Ann. Chem., 1907, 351, 255. [all data]
Moureu and Delange, 1903
Moureu; Delange,
Bull. Soc. Chim. Fr., 1903, 29, 672. [all data]
Louguinine, 1898
Louguinine, W.,
Study of Latent Heats of Vaporizaion of Some Liquids,
Ann. Chim. Phys., 1898, 13, 289-377. [all data]
Behal, 1888
Behal, A.,
Ann. Chim. Phys., 1888, 15, 267. [all data]
Winogradow, 1878
Winogradow, W.,
Justus Liebigs Ann. Chem., 1878, 191, 125. [all data]
Munch, 1876
Munch, R.,
Justus Liebigs Ann. Chem., 1876, 180, 327. [all data]
Frankland and Duppa, 1866
Frankland, E.; Duppa, B.F.,
Justus Liebigs Ann. Chem., 1866, 138, 328. [all data]
Notes
Go To: Top, Normal boiling point, References
- Symbols used in this document:
Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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