Decane

Formula: C₁₀H₂₂
Molecular weight: 142.2817
IUPAC Standard InChI: InChI=1S/C10H22/c1-3-5-7-9-10-8-6-4-2/h3-10H2,1-2H3
IUPAC Standard InChIKey: DIOQZVSQGTUSAI-UHFFFAOYSA-N
CAS Registry Number: 124-18-5
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-Decane; n-C10H22; UN 2247
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Normal boiling point

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Data compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

T_boil (K)	Reference	Comment
447.3	Weast and Grasselli, 1989	BS
447.3	Gierycz, Gregorowicz, et al., 1988	Uncertainty assigned by TRC = 0.1 K; TRC
447.3	Majer and Svoboda, 1985
447.75	Kurtyka and Kurtyka, 1979	Uncertainty assigned by TRC = 0.3 K; TRC
447.25	Treszczanowicz and Treszczanowicz, 1979	Uncertainty assigned by TRC = 0.08 K; TRC
447.15	Cooper, Crowne, et al., 1967	Uncertainty assigned by TRC = 0.5 K; not clear if this is their measurement; TRC
447.3	Gilmour, Zwicker, et al., 1967	Uncertainty assigned by TRC = 0.5 K; TRC
447.15	Trabczynski, 1964	Uncertainty assigned by TRC = 0.3 K; TRC
447.25	Maczynska and Zieborak, 1963	Uncertainty assigned by TRC = 0.3 K; TRC
447.75	Kurtyka, 1961	Uncertainty assigned by TRC = 0.2 K; TRC
446.65	Zieborak and Wyrzykowska-Stankiewicz, 1958	Uncertainty assigned by TRC = 0.25 K; TRC; Data excluded from overall average
447.27	Desty and Whyman, 1957	Uncertainty assigned by TRC = 0.3 K; TRC
447.15	Zieborak and Brzostowski, 1957	Uncertainty assigned by TRC = 0.2 K; TRC
447.2	Gupta, 1956	Uncertainty assigned by TRC = 0.5 K; TRC
447.37	Hansen and Hansen, 1955	Uncertainty assigned by TRC = 0.25 K; TRC
446.95	Zieborak, Kaczorowna-Badyoczek, et al., 1955	Uncertainty assigned by TRC = 0.4 K; TRC
447.15	Colonge and Berthoud, 1952	Uncertainty assigned by TRC = 1. K; TRC
447.26	Mears, Fookson, et al., 1950	Uncertainty assigned by TRC = 0.08 K; TRC
446.5	Mumford and Phillips, 1950	Uncertainty assigned by TRC = 0.5 K; TRC; Data excluded from overall average
447.27	Boord, Henne, et al., 1949	Uncertainty assigned by TRC = 0.3 K; TRC
447.4	Foehr and Fenske, 1949	Uncertainty assigned by TRC = 0.4 K; TRC
447.37	Manning and Kincannon, 1949	Uncertainty assigned by TRC = 0.3 K; TRC
447.3	Tilicheev and Milovidova, 1949	Uncertainty assigned by TRC = 0.6 K; TRC
447.2	Fenske, Braun, et al., 1947	Uncertainty assigned by TRC = 0.3 K; TRC
447.27	Boord, Greenlee, et al., 1946	Uncertainty assigned by TRC = 0.3 K; TRC
447.27	Forziati, Glasgow, et al., 1946	Uncertainty assigned by TRC = 0.01 K; TRC
447.3	Anonymous, 1944	Uncertainty assigned by TRC = 0.3 K; TRC
447.35	McArdle and Robertson, 1943	Uncertainty assigned by TRC = 0.5 K; TRC
447.28	Willingham, 1943	Uncertainty assigned by TRC = 0.3 K; TRC
447.1	Gibson, 1938	Uncertainty assigned by TRC = 1. K; TRC
444.45	Kohlraush and Koppl, 1934	Uncertainty assigned by TRC = 1.5 K; TRC; Data excluded from overall average
447.15	Bruun and Hicks-Brunn, 1932	Uncertainty assigned by TRC = 0.2 K; TRC
447.1	Chavanne and Tock, 1932	Uncertainty assigned by TRC = 0.5 K; TRC
447.17	Mair, 1932	Uncertainty assigned by TRC = 0.1 K; TRC
447.21	Shepard, Henne, et al., 1931	Uncertainty assigned by TRC = 0.15 K; TRC
446.9	Simon, 1929	Uncertainty assigned by TRC = 0.3 K; TRC
445.15	Sakami, 1928	Uncertainty assigned by TRC = 2. K; TRC; Data excluded from overall average
444.65	Schutz, Buschmann, et al., 1924	Uncertainty assigned by TRC = 2. K; TRC; Data excluded from overall average
447.	Pictet and Potok, 1919	Uncertainty assigned by TRC = 6. K; TRC
446.15	Lagerlof, 1918	Uncertainty assigned by TRC = 1.5 K; TRC; Data excluded from overall average
445.15	Zappi, 1916	Uncertainty assigned by TRC = 3. K; identity assumed; TRC; Data excluded from overall average
446.15	Engler and Halmai, 1910	Uncertainty assigned by TRC = 2. K; TRC; Data excluded from overall average
430.7	Landolt and Jahn, 1892	Uncertainty assigned by TRC = 1.5 K; TRC; Data excluded from overall average

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:

References

Go To: Top, Normal boiling point, Notes

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]

Gierycz, Gregorowicz, et al., 1988
Gierycz, P.; Gregorowicz, J.; Malanowski, S., Vapor Pressures and Excess Gibbs Energies of (Butan-1-ol+n-octane or n-Decane) at 373,15 and 383.15 K, J. Chem. Thermodyn., 1988, 20, 385. [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]

Kurtyka and Kurtyka, 1979
Kurtyka, Z.M.; Kurtyka, E.A., Vapor-Liquid Equilibria in the Systems Aniline-Pseudocumene, o-Toluidine-n-Decane, and m-Xylidine-n-Dodecane at Atmos. Press., J. Chem. Eng. Data, 1979, 24, 15. [all data]

Treszczanowicz and Treszczanowicz, 1979
Treszczanowicz, T.; Treszczanowicz, A.J., Vapor-Liquid Phase Equilibria of Binary Systems Formed by Pentane-1-ol and Alkanes, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1979, 27, 689-95. [all data]

Cooper, Crowne, et al., 1967
Cooper, A.R.; Crowne, C.W.P.; Farrell, P.G., Gas-Liquid Chromatographic Studies of Electron-Donor-Acceptor Systems, Trans. Faraday Soc., 1967, 63, 447. [all data]

Gilmour, Zwicker, et al., 1967
Gilmour, J.B.; Zwicker, J.O.; Katz, J.; Scott, R.L., Fluorocarbon Solutions at Low Temperatures V. The Liquid Mixtures C2H6 + C2F6m, C3H8 + C2F6, CH4 + C3F8, C2H6 + C3F8, C3H8 + C3F8, n-C4H10 + C3F8, i-C4H10 + C3F8, C3H8 + n-C4F10, n-C6H14 + n-C4F10, n, J. Phys. Chem., 1967, 71, 3259. [all data]

Trabczynski, 1964
Trabczynski, W., Location of saddle points in the series of systems formed by propionic acid, 2-picoline and n-paraffins, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1964, 12, 335. [all data]

Maczynska and Zieborak, 1963
Maczynska, Z.; Zieborak, K., Vapour-liquid equilibria. binary systems pyridine-n-paraffins under constant pressure. I, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1963, 11, 219. [all data]

Kurtyka, 1961
Kurtyka, Z., Series of Binary Azeotropes Formed by Aniline, o-Toluidine and m-Xylidine with Normal Paraffinic Hydrocarbons, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1961, 9, 745. [all data]

Zieborak and Wyrzykowska-Stankiewicz, 1958
Zieborak, K.; Wyrzykowska-Stankiewicz, D., A series of ternary positive-negative azeotropes formed by 2-picoline, acetic acid and n-paraffins, Bull. Acad. Pol. Sci., Ser. Sci., Chim., Geol. Geogr., 1958, 6, 377. [all data]

Desty and Whyman, 1957
Desty, D.H.; Whyman, B.H.F., Anal. Chem., 1957, 29, 320. [all data]

Zieborak and Brzostowski, 1957
Zieborak, K.; Brzostowski, W., Vapour-liquid equilibria. II. the n-decane-acetic acid-2,6-lutidine system, Bull. Acad. Pol. Sci., Cl. 3, 1957, 5, 309. [all data]

Gupta, 1956
Gupta, V.S., Boiling Point and Critical Temperature of n-Paraffins, J. Chem. Phys., 1956, 24, 164. [all data]

Hansen and Hansen, 1955
Hansen, R.S.; Hansen, R.D., J. Phys. Chem., 1955, 59, 496. [all data]

Zieborak, Kaczorowna-Badyoczek, et al., 1955
Zieborak, K.; Kaczorowna-Badyoczek, H.; Maczynska, Z., Azeotropic and polyazeotropic systems. XX. the positive - negative azeotropes formed by 2,6-lutidine, acetic acid and paraffinic hydrocarbons, Rocz. Chem., 1955, 29, 783. [all data]

Colonge and Berthoud, 1952
Colonge, J.; Berthoud, J., The Preparation of Several Pure Hydrocarbons, Bull. Soc. Chim. Fr., 1952, 1952, 211. [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]

Mumford and Phillips, 1950
Mumford, S.A.; Phillips, J.W.C., 19. The Physical Properties of Some Aliphatic Compounds, J. Chem. Soc., 1950, 1950, 75-84. [all data]

Boord, Henne, et al., 1949
Boord, C.E.; Henne, A.L.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Grignard Reagent in hydrocarbon synthesis, Ind. Eng. Chem., 1949, 41, 609. [all data]

Foehr and Fenske, 1949
Foehr, E.G.; Fenske, M.R., Magneto-optic Rotation of Hydrocarbons, Ind. Eng. Chem., 1949, 41, 1956. [all data]

Manning and Kincannon, 1949
Manning; Kincannon, Ind. Eng. Chem., 1949, 47, 149. [all data]

Tilicheev and Milovidova, 1949
Tilicheev, M.D.; Milovidova, N.V., Isolation of individual hydrocarbons from a paraffin cracking distillate: II isolation of n-alkanes and 1-alkenes with the carbon atom number from five to eleven, Zh. Prikl. Khim. (Leningrad), 1949, 22, 611-24. [all data]

Fenske, Braun, et al., 1947
Fenske, M.R.; Braun, W.G.; Wiegand, R.V.; Quiggle, D.; McCormick, R.H.; Rank, D.H., Raman Spectra of Hydrocarbons, Anal. Chem., 1947, 19, 700. [all data]

Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]

Forziati, Glasgow, et al., 1946
Forziati, A.F.; Glasgow, A.R.; Willingham, C.B.; Rossini, F.D., Specification adn Properties of 29 Paraffin, 4 Alkylcyclopentanes, 10 Alkylcyclohexanes and 8 Alkylbenzene Hydrocarbons, J. Res. Natl. Bur. Stand. (U. S.), 1946, 36, 129. [all data]

Anonymous, 1944
Anonymous, R., , Sunbury Rep., Anglo-Iranian Oil Co., March 22, 1944. [all data]

McArdle and Robertson, 1943
McArdle, E.H.; Robertson, A.E., Ind. Eng. Chem., Anal. Ed., 1943, 15, 484. [all data]

Willingham, 1943
Willingham, C.B., , Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1943. [all data]

Gibson, 1938
Gibson, J.D., Olefins of Types I and II from Butadiene and the Relation of Their Physical Constants to Structure, Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1938. [all data]

Kohlraush and Koppl, 1934
Kohlraush, K.W.F.; Koppl, F., Z. Phys. Chem., Abt. B, 1934, 26, 209. [all data]

Bruun and Hicks-Brunn, 1932
Bruun, J.H.; Hicks-Brunn, M.M., Isolation of normal decane from petroleum by distillation and equilibrium melting, J. Res. Natl. Bur. Stand. (U. S.), 1932, 8, 583. [all data]

Chavanne and Tock, 1932
Chavanne, G.; Tock, G., Slow Oxidation of Saturated Normal Acyclic Hydrocarbons: Octane, Nonane, Decane, Bull. Soc. Chim. Belg., 1932, 41, 630. [all data]

Mair, 1932
Mair, B.J., The Synthesis, Purification, and Certain Physical Constants of the Normal Hydrocarbons from Pentane to Dodecane, of n-Amyl Bromide and of n-Nonyl Bromide, J. Res. Natl. Bur. Stand. (U. S.), 1932, 9, 457. [all data]

Shepard, Henne, et al., 1931
Shepard, A.F.; Henne, A.L.; Midgley, T., Physical Prop. of the Normal Paraffin Hydrocarbons Pentane to Dodecane, J. Am. Chem. Soc., 1931, 53, 1948. [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]

Sakami, 1928
Sakami, S., Mem. Coll. Sci., Univ. Kyoto, Ser. A, 1928, 11, 505. [all data]

Schutz, Buschmann, et al., 1924
Schutz, F.; Buschmann, W.; Wissebach, H., Chem. Ber., 1924, 57, 421. [all data]

Pictet and Potok, 1919
Pictet, A.; Potok, J., The Distillation of Sodium Stearate and Oleate Under Reduced Pressure and the Origin of Petroleum, Helv. Chim. Acta, 1919, 2, 501. [all data]

Lagerlof, 1918
Lagerlof, D., Thermodynamic research: reduced formulas for simplified calculations of latent molar heat of evaporation, J. Prakt. Chem., 1918, 98, 136. [all data]

Zappi, 1916
Zappi, E.V., Organomagnesium Derivatives of 1,5-Dichloropentane, Bull. Soc. Chim. Fr., 1916, 19, 247. [all data]

Engler and Halmai, 1910
Engler, C.; Halmai, B., Chem. Ber., 1910, 43, 397. [all data]

Landolt and Jahn, 1892
Landolt, H.; Jahn, H., The Molecular Refraction of Several Simple Organic Compounds for Rays of Infinitely Great Wave Length., Z. Phys. Chem., Stoechiom. Verwandtschaftsl., 1892, 10, 289. [all data]

Notes

Go To: Top, Normal boiling point, References

Symbols used in this document:

T_boil Boiling point
Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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