1-Heptanol

• Formula: C₇H₁₆O
• Molecular weight: 116.2013
• IUPAC Standard InChI: InChI=1S/C7H16O/c1-2-3-4-5-6-7-8/h8H,2-7H2,1H3 Copy

  
• IUPAC Standard InChIKey: BBMCTIGTTCKYKF-UHFFFAOYSA-N Copy
• CAS Registry Number: 111-70-6
• 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.
• Species with the same structure:
  • Heptanol
• Other names: Heptyl alcohol; n-Heptan-1-ol; n-Heptanol; n-Heptyl alcohol; Enanthic alcohol; Gentanol; 1-Hydroxyheptane; n-C7H15OH; Heptan-1-ol; Heptane-1-ol; Heptyl alcohol, n-; n-Heptanol-1; l'Alcool n-heptylique primaire; Alcohol C7; Enanthyl alcohol; 1-Heptyl alcohol; Heptanol-1; NSC 3703; 1-HeptanoI
• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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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

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]

Kowalski, Kasprzycka-Guttman, et al., 1976
Kowalski, B.; Kasprzycka-Guttman, T.; Orszagh, A., Excess volumes of binary mixtures of 2,6-lutidine with alcohols, Rocz. Chem., 1976, 50, 1445. [all data]

Puzitskii, Bulanova, et al., 1970
Puzitskii, K.V.; Bulanova, T.F.; Bin, Y.Y.; Eidus, Y.T., Synthesis of C7-C9 2,2- and 3,3-Dimethylalkanes from Saturated C6-C9 Normal Alcohols, Izv. Akad. Nauk SSSR, 1970, 1970, 1872. [all data]

Colonge and Poilane, 1955
Colonge; Poilane, Bull. Soc. Chim. Fr., 1955, 1955, 953. [all data]

Brewster, 1954
Brewster, J.H., J. Am. Chem. Soc., 1954, 76, 6364. [all data]

McKenna, Tartar, et al., 1953
McKenna, F.E.; Tartar, H.V.; Lingafelter, E.C., Studies of hemiacetal formation in alcohol - aldehyde systems: II refraction studies, J. Am. Chem. Soc., 1953, 75, 604-7. [all data]

Anderson and Smith, 1952
Anderson, D.G.; Smith, J.C., Alkylnaphthalenes: vii the physical properties of the n-alkylnaphthalenes, J. Inst. Pet., 1952, 38, 415. [all data]

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Cook, N.C., , Unpublished, Final Rep.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

Pichler, Ziesecke, et al., 1950
Pichler, H.; Ziesecke, K.H.; Traeger, B., The Oxygen-containing Compounds, Especially Alcohols, Formed in Isosynthesis, Brennst.-Chem., 1950, 31, 361. [all data]

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

McKenna, Tartar, et al., 1949
McKenna, F.E.; Tartar, H.V.; Lingafelter, E.C., Studies of hemiacetal formation in alcohol + aldehyde systems: I cryscopic studies, J. Am. Chem. Soc., 1949, 71, 729-32. [all data]

Tschamler, Richter, et al., 1949
Tschamler, H.; Richter, E.; Wettig, F., Mixtures of Primry Aliphatic Alcohols with Chlorex and Other Organic Substances. Binary Liquid Mixtures XII., Monatsh. Chem., 1949, 80, 749. [all data]

Addison, 1945
Addison, C.C., 26. The Properties of Freshly Formed Surfaces. IV. The Influence of Chain Length and Structure on the Static and the Dynamic Surface Tensions of Aqueous Alcoholic Solutions, J. Chem. Soc., 1945, 1945, 98-106. [all data]

Appleby, Dobratz, et al., 1944
Appleby, W.G.; Dobratz, C.J.; Kapranos, S.W., Vapor Phase Dehydration of 1-Heptanol ofer Activated Alumina, J. Am. Chem. Soc., 1944, 66, 1938. [all data]

Lecat, 1943
Lecat, M., Azeotropes of Ethyl Urethane and other Azeotropes, C. R. Hebd. Seances Acad. Sci., 1943, 217, 273. [all data]

Clarke and Dreger, 1941
Clarke; Dreger, E.E., Organic Synthesis, Collective Vol. 1, 2nd ed., Wiley-- Interscience: New York, p 304, 1941. [all data]

Komarewsky and Coley, 1941
Komarewsky, V.I.; Coley, J.R., Catalytic dehydrogenation and condensation of aliphatic alcohols: II, J. Am. Chem. Soc., 1941, 63, 3269-70. [all data]

Wibaut and Van Pelt, 1938
Wibaut, J.P.; Van Pelt, A.J., Recl. Trav. Chim. Pays-Bas, 1938, 57, 1055. [all data]

Bilterys and Gisseleire, 1935
Bilterys, R.; Gisseleire, J., Investigations on the Congelation Temperature of Organic Compounds, Bull. Soc. Chim. Belg., 1935, 44, 567. [all data]

Butler, Thomson, et al., 1933
Butler, J.A.V.; Thomson, D.W.; Maclennan, W.H., The Free Energy of the Normal Aliphatic Alcohols in Aqueous Solution. Part I. The Partial Vapor Pressures of Aqueous Solutions of Methyl, n-Propyl, and n-Butyl Alcohols. Part II. THe Solubilities of, J. Chem. Soc., 1933, 1933, 674-686. [all data]

Ellis and Reid, 1932
Ellis, L.M.; Reid, E.E., The Preparation and Properties of A Double Series of Aliphatic Mercaptans, J. Am. Chem. Soc., 1932, 54, 1674. [all data]

Deffet, 1931
Deffet, L., The Freezing Points of Organic Compounds XIII. Compounds With Seven Eight, Nine or Ten Carbon Atoms, Bull. Soc. Chim. Belg., 1931, 40, 385-402. [all data]

Lecat, 1930
Lecat, M., Azeotropism in Binary Mixtures Containing an Alcohol Mixed with an amine, a nitro derivative, an ether or water., Z. Anorg. Allg. Chem., 1930, 186, 119. [all data]

Mondain-Monval and Galet, 1930
Mondain-Monval, P.; Galet, P., Anomalies of the Physical Properties of the Vitreous State, C. R. Hebd. Seances Acad. Sci., 1930, 190, 120. [all data]

Senderens and Aboulenc, 1930
Senderens, J.B.; Aboulenc, J., C. R. Hebd. Seances Acad. Sci., 1930, 190, 150. [all data]

Norris and Cortese, 1927
Norris, J.F.; Cortese, F., The reactivity of atoms and groups in organic compounds: II. second contribution on the relative reactivities of the hydroxyl-hydrogen atoms in certain alcohols, J. Am. Chem. Soc., 1927, 49, 2640-50. [all data]

Senderens, 1925
Senderens, J.B., C. R. Hebd. Seances Acad. Sci., 1925, 181, 698. [all data]

Timmermans, 1922
Timmermans, J., Investigation of the Freezing Point of Organic Substances VII, Bull. Soc. Chim. Belg., 1922, 31, 389. [all data]

Behal, 1919
Behal, A., Isolation and characterization of alcohols, Bull. Soc. Chim. Fr., 1919, 25, 473. [all data]

Eykman, 1919
Eykman, J.F., Natuurkd. Verh. Hollandsche Maatschappij Wet. Haarlem, 1919, 8, 438. [all data]

Levene and Taylor, 1918
Levene, P.A.; Taylor, F.A., J. Biol. Chem., 1918, 35, 281. [all data]

Harries, 1916
Harries, C.D., Ozone and Its Action on Organic Compound, 1916. [all data]

Willcox and Brunel, 1916
Willcox, M.; Brunel, R.F., J. Am. Chem. Soc., 1916, 38, 1821. [all data]

Ohta, 1914
Ohta, T., Biochem. Z., 1914, 59, 183. [all data]

Vavon, 1914
Vavon, G., Hydrogeneration catalyst in the presence of platinum blacks. Transformation of aldehydes and ketones to alcohols, Ann. Chim. (Paris), 1914, 1, 144-200. [all data]

Skita and Meyer, 1912
Skita, A.; Meyer, W.A., Chem. Ber., 1912, 45, 3589. [all data]

Falk, 1909
Falk, K.G., The change in refractive index with temperature, J. Am. Chem. Soc., 1909, 31, 86. [all data]

Van Gysegem, 1906
Van Gysegem, J., Bull. Cl. Sci., 1906, 1906, 692. [all data]

Guerbet, 1901
Guerbet, M., C. R. Hebd. Seances Acad. Sci., 1901, 132, 207. [all data]

Gartenmeister, 1886
Gartenmeister, R., Investigation of the physical characterstics of liquid compounds: vi boiling point and specific volume of normal fatty acid esters, Justus Liebigs Ann. Chem., 1886, 233, 249-315. [all data]

Perkin, 1884
Perkin, W.H., On the Magnetic Rotary Polarisation of Compounds in Relation to their Chemical Consitution; with Observations on the Preparation and Relative Densities of the Bodies Examined, J. Chem. Soc., 1884, 45, 421-580. [all data]

Zander, 1884
Zander, A., The specific volumes of liquid compounds: IV normal fatty acids and normal fatty alcohols, Justus Liebigs Ann. Chem., 1884, 224, 56-95. [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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