4-Heptanol

• Formula: C₇H₁₆O
• Molecular weight: 116.2013
• IUPAC Standard InChI: InChI=1S/C7H16O/c1-3-5-7(8)6-4-2/h7-8H,3-6H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: YVBCULSIZWMTFY-UHFFFAOYSA-N Copy
• CAS Registry Number: 589-55-9
• 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: Dipropylcarbinol; CH3(CH2)2CHOH(CH2)2CH3; di-n-Propylcarbinol; n-Heptan-4-ol; Heptanol-4; heptan-4-ol
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• 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
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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 by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

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

Shuikin and Bel'skii, 1956
Shuikin, N.I.; Bel'skii, I.F., Hydrogenation and Hydrogenolysis of alpha-Ethyl and alpha-Propenyl- furan on Raney Nickel Catalyst, J. Gen. Chem. USSR (Engl. Transl.), 1956, 26, 3025. [all data]

Kornblum, Smiley, et al., 1955
Kornblum, N.; Smiley, R.A.; Ungnade, H.E.; White, A.M.; Taub, B., The reaction of silver nitrite with secondary and tertiary alkyl halides, J. Am. Chem. Soc., 1955, 77, 5528-33. [all data]

Haszeldine, 1953
Haszeldine, R.N., J. Chem. Soc., 1953, 1953, 1757. [all data]

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Cook, N.C., , Unpublished, Final Rep.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

Rust, Seubold, et al., 1948
Rust, F.F.; Seubold, F.H.; Vaughan, W.E., Formation of secondary alcohols in the free radical decomposition of aldehydes., J. Am. Chem. Soc., 1948, 70, 4253. [all data]

Boeseken and Hanegraaff, 1942
Boeseken, J.; Hanegraaff, J.A., Recl. Trav. Chim. Pays-Bas, 1942, 61, 69. [all data]

Goldwasser and Taylor, 1939
Goldwasser, S.; Taylor, H.S., Catalytic dehydration of c6-c8 aliphatic alcohols, J. Am. Chem. Soc., 1939, 61, 1751. [all data]

Suknevich and Chilingaryan, 1936
Suknevich; Chilingaryan, Chem. Ber., 1936, 69, 1537. [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]

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

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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