Tetracosane

• Formula: C₂₄H₅₀
• Molecular weight: 338.6538
• IUPAC Standard InChI: InChI=1S/C24H50/c1-3-5-7-9-11-13-15-17-19-21-23-24-22-20-18-16-14-12-10-8-6-4-2/h3-24H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: POOSGDOYLQNASK-UHFFFAOYSA-N Copy
• CAS Registry Number: 646-31-1
• 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-Tetracosane
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal melting 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

Go To: Top, Normal melting point, Notes

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

Domanska, Lachwa, et al., 1999
Domanska, U.; Lachwa, J.; Morawski, P., Phase Equil. and Vol. Prop. in Binary Mixt. Cont. Branched Chain Ethers (Methyl 1,1-Dimethylethyl Ether or Ethyl 1,1-Dimethylethyl Ether or Methyl 1,1-Dimethylpropyl Ether or Ethyl 1,1-Dimethylpropyl, J. Chem. Eng. Data, 1999, 44, 974-84. [all data]

Estrera and Luks, 1987
Estrera, S.S.; Luks, K.D., Liquid-Liquid-Vapor Equil. Behavior of Certain Ethane + n-Paraffin Mix, J. Chem. Eng. Data, 1987, 32, 201. [all data]

Company, 1973
Company, J.-C., Measurement and Interpretation of Crystallization Equilibrium of Heavy Paraffin and Aromatic Hydrocarbon Solutions, Chem. Eng. Sci., 1973, 28, 318. [all data]

Anonymous, 1968
Anonymous, R., Properties of hydrocarbon of high molecular weight, Am. Pet. Inst. Res. Proj. 42, Penn. State Univ., 1968. [all data]

Cason and Fessenden, 1957
Cason, J.; Fessenden, R.J., Reactivity of Organocadmium Reagents Toward Halides Other Than Acid Acid Chlorides. Improvemenet of Conditions for the Reformatskii Reaction, J. Org. Chem., 1957, 22, 1326-32. [all data]

Sondheimer, Amiel, et al., 1957
Sondheimer, F.; Amiel, Y.; Wolovsky, R., Unsaturated Macrocyclic Compounds IV. The Oxidation of Terminal Diacetylenes to Macrocyclic Tetraacetaylenes, J. Am. Chem. Soc., 1957, 79, 6263. [all data]

Marculaitis, 1956
Marculaitis, W.J., , Ph.D. Thesis, Carnegie Inst. Technol., Pittsburgh, 1956. [all data]

Templin, 1956
Templin, P.R., Coefficient of volume expansion for petroleum waxes and pure n-paraffins, Ind. Eng. Chem., 1956, 48, 154. [all data]

Kirrmann and Geiger-Berschandy, 1955
Kirrmann, A.; Geiger-Berschandy, M.S., Bull. Soc. Chim. Fr., 1955, 1955, 991. [all data]

Schaerer, Busso, et al., 1955
Schaerer, A.A.; Busso, C.J.; Smith, A.E.; Skinner, L.B., Properties of Pure Normal Alkanes in the C17 to C36 Range, J. Am. Chem. Soc., 1955, 77, 2017-8. [all data]

Hoffman and Decker, 1953
Hoffman, J.D.; Decker, B.F., Solid state phase changes in long chain compounds., J. Phys. Chem., 1953, 57, 520-29. [all data]

Fritz-Brini and Berschandy, 1951
Fritz-Brini; Berschandy, C. R. Hebd. Seances Acad. Sci., 1951, 232, 524. [all data]

Parks, Moore, et al., 1949
Parks, G.S.; Moore, G.E.; Renquist, M.L.; Naylor, B.F.; McClaine, L.A.; Fujii, P.S.; Hatton, J.A., Thermal Data on Organic Compounds. XXV. Some Heat Capacity, Entropy and Free Energy Data for Nine Hydrocarbons of High Molecular Weight, J. Am. Chem. Soc., 1949, 71, 10, 3386, https://doi.org/10.1021/ja01178a034 . [all data]

Mazee, 1948
Mazee, W.M., Some properties of hydrocarbons having more than twenty carbon atoms, Recl. Trav. Chim. Pays-Bas, 1948, 67, 197-213. [all data]

Schiessler, 1947
Schiessler, R.W., , Am. Pet. Inst. Res. Proj. 42, Twelfth Meeting, 1947. [all data]

Seyer, Patterson, et al., 1944
Seyer, W.F.; Patterson, R.F.; Keays, J.L., The Density and Transition Points of the n-Paraffin Hydrocarbons, J. Am. Chem. Soc., 1944, 66, 179-82. [all data]

Van Hook and Silver, 1942
Van Hook, A.; Silver, L., Premelting Anomalies of Some Long-Chain Normal Paraffin Hydrocarbons, J. Chem. Phys., 1942, 10, 686-90. [all data]

Turkiewicz, 1939
Turkiewicz, N., Chem. Ber., 1939, 72, 1060. [all data]

Ziegler, Dersch, et al., 1934
Ziegler, K.; Dersch, F.; Wollthan, H., Alkali Organic Compounds XI. Mechanism of Polymerizationof Unsaturated Hydrocarbons by Alkali Metal and Alkali ALkyls, Justus Liebigs Ann. Chem., 1934, 511, 13-44. [all data]

Mueller, 1932
Mueller, A., Proc. R. Soc. London, A, 1932, 138, 514. [all data]

Mueller, 1930
Mueller, A., Proc. R. Soc. London, A, 1930, 127, 417. [all data]

Mueller and Saville, 1925
Mueller, A.; Saville, W.B., J. Chem. Soc., 1925, 127, 599. [all data]

McKinney, 1924
McKinney, J.W., J. Am. Chem. Soc., 1924, 46, 968. [all data]

Easterfield and McClelland, 1923
Easterfield, T.H.; McClelland, N., J. Soc. Chem. Ind., London, Trans. Commun., 1923, 42, 936. [all data]

Fromm and Eckardt, 1923
Fromm, E.; Eckardt, H., Chem. Ber., 1923, 56, 948. [all data]

Hofmann and Damm, 1923
Hofmann, F.; Damm, P., Brennst.-Chem., 1923, 4, 65. [all data]

Ciusa and Vois, 1922
Ciusa, R.; Vois, R., Gazz. Chim. Ital., 1922, 52, 135. [all data]

Gluud, 1919
Gluud, W., Chem. Ber., 1919, 52, 1039. [all data]

Levene and West, 1914
Levene, P.A.; West, C.J., J. Biol. Chem., 1914, 18, 477. [all data]

Mabery, 1905
Mabery, C.F., Am. Chem. J., 1905, 33, 280. [all data]

Mabery, 1902
Mabery, C.F., Am. Chem. J., 1902, 28, 190. [all data]

Krafft, 1883
Krafft, F., Chem.-Ztg., 1883, 7, 153. [all data]

Krafft, 1882
Krafft, F., On Nineteen Higher Normal Paraffins and a Simple Volume Law for Liquids that form Drops I., Ber. Dtsch. Chem. Ges., 1882, 15, 1687-711. [all data]

Krafft, 1882, 2
Krafft, F., Nineteen higher normal paraffins CnH2n+2 and a simple volume law for the saturated liquid state., Ber. Dtsch. Chem. Ges., 1882, 15, 1711. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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