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Butanenitrile

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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

Tboil (K) Reference Comment
389.2Aldrich Chemical Company Inc., 1990BS
391.2Weast and Grasselli, 1989BS
390.8Majer and Svoboda, 1985 
391.1Mato and Benito, 1985Uncertainty assigned by TRC = 0.4 K; TRC
389.Gagnon, Boivin, et al., 1956Uncertainty assigned by TRC = 3. K; TRC
390.6Bruylants, Tits, et al., 1952Uncertainty assigned by TRC = 1. K; TRC
390.7Lewis and Susi, 1952Uncertainty assigned by TRC = 4. K; TRC
390.7Walker, 1952Uncertainty assigned by TRC = 1. K; TRC
390.7Boivin, 1950Uncertainty assigned by TRC = 2. K; TRC
391.1Lecat, 1949Uncertainty assigned by TRC = 0.5 K; TRC
388.Bergstrom and Agostinho, 1945Uncertainty assigned by TRC = 10. K; TRC; Data excluded from overall average
391.Olin, 1945Uncertainty assigned by TRC = 6. K; TRC
391.Teter and Merwin, 1945Uncertainty assigned by TRC = 3. K; TRC
389.7Drozdov and Bekhli, 1944Uncertainty assigned by TRC = 4. K; TRC
387.Karve and Gharpure, 1939Uncertainty assigned by TRC = 5. K; TRC; Data excluded from overall average
391.Condo, Hinkel, et al., 1937Uncertainty assigned by TRC = 2. K; TRC
390.45Butler and Ramchandani, 1935Uncertainty assigned by TRC = 0.3 K; TRC
391.1Timmermans and Delcourt, 1934Uncertainty assigned by TRC = 0.4 K; TRC
390.8De Mol, 1927Uncertainty assigned by TRC = 0.5 K; TRC
390.8Timmermans, 1927Uncertainty assigned by TRC = 0.4 K; source of data not clear; TRC
390.4Timmermans, 1927Uncertainty assigned by TRC = 0.5 K; TRC
391.7Mailhe, 1918Uncertainty assigned by TRC = 1.5 K; TRC
391.Mailhe, 1918, 2Uncertainty assigned by TRC = 1.5 K; TRC
391.Henry, 1905Uncertainty assigned by TRC = 1.5 K; TRC
389.80Van Erp, 1895Uncertainty assigned by TRC = 2. K; TRC

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

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]

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]

Mato and Benito, 1985
Mato, F.; Benito, G.G., Liquid-Vapor Equilibrium of Binary Mixtures of Nitriles and Alcohols. I., An. Quim., Ser. A, 1985, 81, 116. [all data]

Gagnon, Boivin, et al., 1956
Gagnon, P.E.; Boivin, J.L.; Haggart, Catherine, Reactions of Ammonium Sulfamate With Amides and Ureas., Can. J. Chem., 1956, 34, 1662. [all data]

Bruylants, Tits, et al., 1952
Bruylants; Tits; Dieu; Gauthier, Directed chlorination: II aliphatic acids and nitriles; alkyl acetates, Bull. Soc. Chim. Belg., 1952, 61, 366. [all data]

Lewis and Susi, 1952
Lewis, R.N.; Susi, P.V., Synthesis of nitriles in ethylene glycol, J. Am. Chem. Soc., 1952, 74, 840. [all data]

Walker, 1952
Walker, E.E., J. Appl. Chem., 1952, 2, 470. [all data]

Boivin, 1950
Boivin, J.S., Synthesis of nitriles by fusion of amides with ammonium sulphamate, Can. J. Res., Sect. B, 1950, 28, 671. [all data]

Lecat, 1949
Lecat, M., Tables Azeotropiques, Vol. 1, 10th ed., Brussels, Belgium, 1949. [all data]

Bergstrom and Agostinho, 1945
Bergstrom, F.W.; Agostinho, R., The alkylation and arylation of aliphatic nitriles in liquid ammonia, J. Am. Chem. Soc., 1945, 67, 2152. [all data]

Olin, 1945
Olin, J., , 1945. [all data]

Teter and Merwin, 1945
Teter, J.; Merwin, W., , 1945. [all data]

Drozdov and Bekhli, 1944
Drozdov, N.S.; Bekhli, A.F., Reaction of Imido Esters With Some Primary Amines and Ammonia., Zh. Obshch. Khim., 1944, 14, 280. [all data]

Karve and Gharpure, 1939
Karve; Gharpure, J. Univ. Bombay, Sci., 1939, 8, 139. [all data]

Condo, Hinkel, et al., 1937
Condo, F.E.; Hinkel, E.T.; Fassero, A.; Shriner, R.L., Identification of Nitriles. II. Addition Compounds of Nitriles with Mercaptoacetic Acid., J. Am. Chem. Soc., 1937, 59, 230. [all data]

Butler and Ramchandani, 1935
Butler, J.A.V.; Ramchandani, C.N., The Solubility of Non-electrolytes. Part II. The Influence of the Polar Group on the Free Energy of Hydration of Aliphatic Compounds., J. Chem. Soc., 1935, 1935, 952. [all data]

Timmermans and Delcourt, 1934
Timmermans, J.; Delcourt, Y., Work of the International Bureau of Physico-Chemical Standards.VI. Physical Constants of Twenty Organic Compounds., J. Chim. Phys. Phys.-Chim. Biol., 1934, 31, 85-121. [all data]

De Mol, 1927
De Mol, A., Bull. Soc. Chim. Belg., 1927, 36, 509. [all data]

Timmermans, 1927
Timmermans, J., The Melting Point of Organic Substances, Bull. Soc. Chim. Belg., 1927, 36, 502. [all data]

Mailhe, 1918
Mailhe, A., C. R. Hebd. Seances Acad. Sci., 1918, 166, 121. [all data]

Mailhe, 1918, 2
Mailhe, A., Direct Transformation of secondary and tertiary amines to nitriles, C. R. Hebd. Seances Acad. Sci., 1918, 166, 996. [all data]

Henry, 1905
Henry, L., Recl. Trav. Chim. Pays-Bas, 1905, 24, 348. [all data]

Van Erp, 1895
Van Erp, M.H., Recl. Trav. Chim. Pays-Bas, 1895, 14, 15. [all data]


Notes

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