3-Pentanol, 2,2-dimethyl-

• Formula: C₇H₁₆O
• Molecular weight: 116.2013
• IUPAC Standard InChI: InChI=1S/C7H16O/c1-5-6(8)7(2,3)4/h6,8H,5H2,1-4H3 Copy

  
• IUPAC Standard InChIKey: HMSVXZJWPVIVIV-UHFFFAOYSA-N Copy
• CAS Registry Number: 3970-62-5
• 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: 2,2-Dimethyl-3-pentanol; 2,2-dimethylpentan-3-ol
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • Ion clustering 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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - 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.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Foley, Welch, et al., 1959
Foley, W.M.; Welch, F.J.; La Combe, E.; Mosher, H.S., Asymmetric reductions: vi the action of the grignard reagent from (+)-1- chloro-2-methylbutane on a series of alkyl t-butyl ketones, J. Am. Chem. Soc., 1959, 81, 2779. [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]

Boord, Greenlee, et al., 1949
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Wt., Am. Pet. Inst. Res. Proj. 45, Eleventh Annu. Rep., Ohio State Univ., 1949. [all data]

James, 1943
James, W.H., , Ph.D. Thesis, Penn. State Univ., Univ. Park, PA, 1943. [all data]

Stevens and Mccoubrey, 1941
Stevens, P.G.; Mccoubrey, J.A., J. Am. Chem. Soc., 1941, 63, 2847. [all data]

Cramer and Miller, 1940
Cramer, P.L.; Miller, V.A., The Thermal Decomposition of the Acetate of 2,2-Dimethyl-3-pentanol, J. Am. Chem. Soc., 1940, 62, 1452. [all data]

Wibaut, Hoog, et al., 1939
Wibaut, J.P.; Hoog, H.; Langedijk, S.L.; Overhoff, J.; Smittenberg, J.; Benninga, N.; Bouman, G.P.; van Dijk, H.; Gaade, W.; Geldof, H.; Hackmann, J.Th.; Jonker, E.W.; Paap, T.; Zuiderweg, F.J., Study on the Preparation and the Physical Constants of A Number of Alkanes and Cycloalkanes, Recl. Trav. Chim. Pays-Bas, 1939, 58, 329. [all data]

Ginnings and Hauser, 1938
Ginnings, P.M.; Hauser, M., Aqueous solubilities of some isomeric heptanols, J. Am. Chem. Soc., 1938, 60, 2581-2582. [all data]

Edgar, Calingaert, et al., 1929
Edgar, G.; Calingaert, G.; Marker, R.E., Preparation and Properties of the Isomeric Heptanes I. Preparation Preparation., J. Am. Chem. Soc., 1929, 51, 1483. [all data]

Leroide, 1921
Leroide, J., Ann. Chim. (Paris), 1921, 16, 354. [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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