Benzene, 1,4-bis(1,1-dimethylethyl)-

• Formula: C₁₄H₂₂
• Molecular weight: 190.3245
• IUPAC Standard InChI: InChI=1S/C14H22/c1-13(2,3)11-7-9-12(10-8-11)14(4,5)6/h7-10H,1-6H3 Copy

  
• IUPAC Standard InChIKey: OOWNNCMFKFBNOF-UHFFFAOYSA-N Copy
• CAS Registry Number: 1012-72-2
• 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: Benzene, p-di-tert-butyl-; p-Di-tert-butylbenzene; 1,4-Di-tert-butylbenzene; Benzene, 1,4-bis-(tert-butyl)
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
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Normal melting 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

Go To: Top, Normal melting point, Notes

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

Arnett, Sanda, et al., 1967
Arnett, E.M.; Sanda, J.C.; Bollinger, J.M.; Barber, M., Crowded benzenes. VI. The strain energy in o-di-tbutylbenzenes, J. Am. Chem. Soc., 1967, 89, 5389. [all data]

Streiff, Schultz, et al., 1960
Streiff, A.J.; Schultz, L.H.; Krouskop, N.C.; Moore, J.W.; Rossini, F.D., Purification, Purity, and Freezing Points of 16 API Standard and API Research Hydrocarbons, J. Chem. Eng. Data, 1960, 5, 193-5. [all data]

Ogimachi, Andrews, et al., 1955
Ogimachi, N.N.; Andrews, L.J.; Keefer, R.M., The Free Energies and Heats of Formation of Polyalkoxybenzene-Iodine Monochloride Complexes, J. Am. Chem. Soc., 1955, 77, 4202. [all data]

Hopke and Sears, 1951
Hopke, E.R.; Sears, G.W., Vapor Pressures below 1 mm Hg of Several Aromatic Compounds, J. Chem. Phys., 1951, 19, 11, 1345, https://doi.org/10.1063/1.1748057 . [all data]

Hennion and Kurtz, 1943
Hennion, G.F.; Kurtz, R.A., Some Friedel-Crafts Type ALkylations with Boron Trifluoride, J. Am. Chem. Soc., 1943, 65, 1001. [all data]

Potts and Carpenter, 1939
Potts, W.M.; Carpenter, L.L., The Condensation of Propene and Isobutene with Benzene in the Presence of Anhdrous Ferric Chloride, J. Am. Chem. Soc., 1939, 61, 663. [all data]

Huston, Fox, et al., 1938
Huston, R.C.; Fox, W.B.; Binder, M.N., Condensation of Aliphatic Alcohols with Aromatic Compounds in the Presence of Aluminum Chloride II. Tertiary Aliphatic Alcohols and Benzene, J. Org. Chem., 1938, 3, 251-60. [all data]

Simons, Archer, et al., 1938
Simons, J.H.; Archer, S.; Passinio, H.J., Hydrogen Fluiride as a Condensing Agent V. Reactions of Compounds Containing Oxygen and Reactions of Tertiary Halides with Olefins, J. Am. Chem. Soc., 1938, 60, 2956. [all data]

Ipatieff, Corson, et al., 1936
Ipatieff, V.N.; Corson, B.B.; Pines, H., Influence of Sulfuric Acid Concentration upon Reaction between Olefins and Benzene, J. Am. Chem. Soc., 1936, 58, 919-22. [all data]

Malishev, 1935
Malishev, B.W., Direct Alkylation of Aromatic Hydrocarbons by Olefins Under Catalytic Influence of Phosphorous Pentoxide, J. Am. Chem. Soc., 1935, 57, 883. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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