Hexane, 3,3-dimethyl-
- Formula: C8H18
- Molecular weight: 114.2285
- IUPAC Standard InChIKey: KUMXLFIBWFCMOJ-UHFFFAOYSA-N
- CAS Registry Number: 563-16-6
- 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. - Other names: 3,3-Dimethylhexane
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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 |
---|---|---|
385.2 | Weast and Grasselli, 1989 | BS |
385.1 | Majer and Svoboda, 1985 | |
384.65 | Puzitskii, Bulanova, et al., 1970 | Uncertainty assigned by TRC = 0.6 K; TRC |
385.13 | Anonymous, 1959 | Uncertainty assigned by TRC = 0.1 K; TRC |
385.12 | Desty and Whyman, 1957 | Uncertainty assigned by TRC = 0.2 K; TRC |
385.0 | Audsley and Goss, 1951 | Uncertainty assigned by TRC = 0.3 K; TRC |
385.05 | Boord, Henne, et al., 1949 | Uncertainty assigned by TRC = 0.3 K; TRC |
385.35 | Denyer, Fidler, et al., 1949 | Uncertainty assigned by TRC = 0.3 K; TRC |
385.1 | Fenske, Braun, et al., 1947 | Uncertainty assigned by TRC = 0.15 K; TRC |
393.05 | Boord, Greenlee, et al., 1946 | Uncertainty assigned by TRC = 0.5 K; TRC; Data excluded from overall average |
385.11 | Forziati, Glasgow, et al., 1946 | Uncertainty assigned by TRC = 0.01 K; TRC |
385.35 | Henne and Chanan, 1944 | Uncertainty assigned by TRC = 0.5 K; TRC |
385.12 | Anonymous, 1942 | Uncertainty assigned by TRC = 0.1 K; TRC |
385.05 | Anonymous, 1941 | Uncertainty assigned by TRC = 0.3 K; TRC |
385.15 | Marker and Oakwood, 1938 | Uncertainty assigned by TRC = 0.5 K; TRC |
385.2 | Dietrich, 1933 | Uncertainty assigned by TRC = 0.5 K; TRC |
384.1 | Schurman and Boord, 1933 | Uncertainty assigned by TRC = 0.6 K; TRC; Data excluded from overall average |
384.65 | Noller, 1929 | Uncertainty assigned by TRC = 1.5 K; TRC |
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]
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]
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]
Anonymous, 1959
Anonymous, R.,
, Am. Pet. Inst. Res. Proj. 6, Carnegie-Mellon Univ., 1959. [all data]
Desty and Whyman, 1957
Desty, D.H.; Whyman, B.H.F.,
Anal. Chem., 1957, 29, 320. [all data]
Audsley and Goss, 1951
Audsley, A.; Goss, F.R.,
Atom Polarisation. Part II. Relationships Between Molecular Dimensions and Boiling Points for Branched-Chain Parafins,
J. Chem. Soc., 1951, 1951, 120-6. [all data]
Boord, Henne, et al., 1949
Boord, C.E.; Henne, A.L.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M.,
The Grignard Reagent in hydrocarbon synthesis,
Ind. Eng. Chem., 1949, 41, 609. [all data]
Denyer, Fidler, et al., 1949
Denyer, R.L.; Fidler, F.A.; Lowry, R.A.,
Azeotrope Formation Between Thiols and Hydrocarbons,
Ind. Eng. Chem., 1949, 41, 2727-37. [all data]
Fenske, Braun, et al., 1947
Fenske, M.R.; Braun, W.G.; Wiegand, R.V.; Quiggle, D.; McCormick, R.H.; Rank, D.H.,
Raman Spectra of Hydrocarbons,
Anal. Chem., 1947, 19, 700. [all data]
Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.,
The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]
Forziati, Glasgow, et al., 1946
Forziati, A.F.; Glasgow, A.R.; Willingham, C.B.; Rossini, F.D.,
Specification adn Properties of 29 Paraffin, 4 Alkylcyclopentanes, 10 Alkylcyclohexanes and 8 Alkylbenzene Hydrocarbons,
J. Res. Natl. Bur. Stand. (U. S.), 1946, 36, 129. [all data]
Henne and Chanan, 1944
Henne, A.L.; Chanan, H.H.,
Diolefins from Allylic Chlorides II.,
J. Am. Chem. Soc., 1944, 66, 392. [all data]
Anonymous, 1942
Anonymous, R.,
, Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1942. [all data]
Anonymous, 1941
Anonymous, R.,
, Am. Pet. Inst. Hydrocarbon Res. Proj., Third Annu. Rep., Ohio State Univ., Aug. 31, 1941. [all data]
Marker and Oakwood, 1938
Marker, R.E.; Oakwood, T.S.,
Hexamethylethane and Tetraalkylmethanes,
J. Am. Chem. Soc., 1938, 60, 2598. [all data]
Dietrich, 1933
Dietrich, M.A.,
Syntheses in the olefin series octenes of type I and type II, Ph.D. Thesis, Ohio State Univ., Columbus, OH, 1933. [all data]
Schurman and Boord, 1933
Schurman, I.; Boord, C.E.,
Synthesis in teh Olefin Series V. Completing the Survey of the Hexenes and Including Certain Heptenes and Octenes,
J. Am. Chem. Soc., 1933, 55, 4930-5. [all data]
Noller, 1929
Noller, C.R.,
The Prep. of Zinc Alkyls and Their Use in the Synthesis of Hydrocarbons,
J. Am. Chem. Soc., 1929, 51, 594. [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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