3-Pentanol

• Formula: C₅H₁₂O
• Molecular weight: 88.1482
• IUPAC Standard InChI: InChI=1S/C5H12O/c1-3-5(6)4-2/h5-6H,3-4H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: AQIXEPGDORPWBJ-UHFFFAOYSA-N Copy
• CAS Registry Number: 584-02-1
• 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: Diethyl carbinol; 3-Pentyl alcohol; (C2H5)2CHOH; Pentan-3-ol; sec-Amyl alcohol; Pentanol-3; UN 2706; Isoamyl alcohol; 1-Ethyl-1-propanol; NSC 8654; sec-Pentanol; sec-Pentyl alcohol
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• 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
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
  • Switch to calorie-based units

Data at NIST subscription sites:

• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Normal boiling point

Go To: Top, References, Notes

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]

Cohen, Borden, et al., 1961
Cohen, H.L.; Borden, D.G.; Minsk, L.N., Reduction of Polymers Using Complex Metal Hydrides II, J. Org. Chem., 1961, 26, 1274. [all data]

Hamelin, 1961
Hamelin, R., Etude des solutions organomagnesiennes mixtures. (5e memoire) action des derives de grinard sur les aldehydes, Bull. Soc. Chim. Fr., 1961, 1961, 926. [all data]

Benkeser, Hazdra, et al., 1959
Benkeser, R.A.; Hazdra, J.J.; Burrous, M.L., Factors influencing the direction of elimination in ester pyrolyses, J. Am. Chem. Soc., 1959, 81, 5374. [all data]

Kharasch, Meltzer, et al., 1957
Kharasch, M.S.; Meltzer, T.H.; Nudenberg, W., J. Org. Chem., 1957, 22, 38. [all data]

Searles, Pollart, et al., 1957
Searles, S.; Pollart, K.A.; Lutz, E.F., Oxetanes: vi reductive cleavage and substituent effects, J. Am. Chem. Soc., 1957, 79, 948-51. [all data]

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]

Pomerantz, Fookson, et al., 1954
Pomerantz, P.; Fookson, A.; Mears, T.W.; Rothberg, S.; Howard, F.L., Synth. and Phys. Prop. of Several Aliphatic and Alicyclic Hydrocarbons hydrocarbons, J. Res. Natl. Bur. Stand. (U. S.), 1954, 52, 59-65. [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]

Zeiss and Tsutsui, 1953
Zeiss, H.H.; Tsutsui, M., The Carbon-Oxygen Absorption Band in the Infrared Spectra of Alcohols, J. Am. Chem. Soc., 1953, 75, 897. [all data]

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

Pines, Rudin, et al., 1952
Pines, H.; Rudin, A.; Ipatieff, V.N., Investigation of the preparation of bromides from 1-, 2- and 3-pentanol systhesis of pure bromopentanes, J. Am. Chem. Soc., 1952, 74, 4063-7. [all data]

Laddha and Smith, 1950
Laddha, G.S.; Smith, J.M., Chem. Eng. Prog., 1950, 46, 195. [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]

Mcmahon, Roper, et al., 1948
Mcmahon, E.M.; Roper, J.N.; Utermohlen, W.P.; Hasek, R.H.; Harris, R.C.; Brant, J.H., Preparation and properties of ethyl vinyl ketone and of methyl isopropenyl ketone, J. Am. Chem. Soc., 1948, 70, 2971-7. [all data]

Lecat, 1947
Lecat, M., Some azeotropes of which one constituant is heterocyclic nitrogen, Ann. Soc. Sci. Bruxelles, Ser. 1, 1947, 61, 73. [all data]

Scattergood, Miller, et al., 1945
Scattergood, A.; Miller, W.H.; Gammon, J., Jr., New Aliphatic Borates, J. Am. Chem. Soc., 1945, 67, 2150. [all data]

Platt, Rusoff, et al., 1943
Platt, J.R.; Rusoff, I.I.; Klevens, H.B., J. Chem. Phys., 1943, 11, 535. [all data]

Jones and McCombie, 1942
Jones, E.R.H.; McCombie, J.T., J. Chem. Soc., 1942, 1942, 733. [all data]

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

Ginnings and Baum, 1937
Ginnings, P.M.; Baum, R., Aqueous Solubilities of the Isomeric Pentanols, J. Am. Chem. Soc., 1937, 59, 1111-1113. [all data]

Sherrill and Matlack, 1937
Sherrill, M.L.; Matlack, L.S., Additional dat on the cis and trans isomers of pentene-2., J. Am. Chem. Soc., 1937, 59, 2134. [all data]

Lespieau and Lombard, 1935
Lespieau, R.; Lombard, R., Bull. Soc. Chim. Fr., 1935, 2, 369. [all data]

Brooks, 1934
Brooks, B.T., J. Am. Chem. Soc., 1934, 56, 1998. [all data]

Packendorff, 1934
Packendorff, K., Chem. Ber., 1934, 67, 905. [all data]

Kohlraush and Koppl, 1933
Kohlraush, K.W.F.; Koppl, F., Monatsh. Chem., 1933, 63, 255. [all data]

Timmermans and Hennaut-Roland, 1932
Timmermans, J.; Hennaut-Roland, M., The Work of the International Bureau of Physical-Chemical Standards. V. Study of the Physical Constants of Twenty Organic Compounds., J. Chim. Phys. Phys.-Chim. Biol., 1932, 29, 529-68. [all data]

Graves, 1931
Graves, G.D., Ind. Eng. Chem., 1931, 23, 1381. [all data]

Kirkpatrick, 1927
Kirkpatrick, Chem. Metall. Eng., 1927, 34, 276. [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]

Van Risseghem, 1914
Van Risseghem, H., Beta-pentene and some of its derivatives, C. R. Hebd. Seances Acad. Sci., 1914, 158, 1694-8. [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]

Timmermans, 1913
Timmermans, J., Bull. Soc. Chim. Belg., 1913, 27, 334. [all data]

Sabatier and Senderens, 1903
Sabatier, P.; Senderens, J.B., C. R. Hebd. Seances Acad. Sci., 1903, 137, 302. [all data]

Ponzio, 1901
Ponzio, G., Gazz. Chim. Ital., 1901, 31, 404. [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
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.