Naphthalene, 2-(1,1-dimethylethyl)-

• Formula: C₁₄H₁₆
• Molecular weight: 184.2768
• IUPAC Standard InChI: InChI=1S/C14H16/c1-14(2,3)13-9-8-11-6-4-5-7-12(11)10-13/h4-10H,1-3H3 Copy

  
• IUPAC Standard InChIKey: MCEORGGPAKTORV-UHFFFAOYSA-N Copy
• CAS Registry Number: 2876-35-9
• 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: Naphthalene, 2-tert-butyl-; β-tert-Butylnaphthalene; 2-tert-Butylnaphthalene; 2-(1,1-Dimethylethyl)naphthalene
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
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Condensed phase thermochemistry data

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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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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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

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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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.

Good and Lee, 1976
Good, W.D.; Lee, S.H., The enthalpies of formation of selected naphthalenes, diphenylmethanes, and bicyclic hydrocarbons, J. Chem. Thermodyn., 1976, 8, 643-650. [all data]

Romadane, 1957
Romadane, I., Zh. Obshch. Khim., 1957, 27, 1939. [all data]

Crawford and Glesmann, 1954
Crawford, H.M.; Glesmann, M.C., 2,6-Di-t-butylnaphthalene, J. Am. Chem. Soc., 1954, 76, 1108. [all data]

Bromby, Peters, et al., 1943
Bromby, N.G.; Peters, A.T.; Rowe, F.M., J. Chem. Soc., 1943, 1943, 144-5. [all data]

Tsukervanik and Terent'eva, 1937
Tsukervanik, I.P.; Terent'eva, I., Condensation of Alcahols with Aromatic Hydrocarbons in the Presence of Anhydrous ALuminum CHloride. IV. Condensation of ALiphatic Alcohols with Naphthalene, Zh. Obshch. Khim., 1937, 7, 637. [all data]

Buu-Hoi and Cagniant, 1942
Buu-Hoi, Ng.Ph.; Cagniant, P., Condensed Aromatic Nuclei IV. Synthesis of Six New Substituted Phenalans, Rev. Sci., 1942, 80, 271. [all data]

Petrov and Andreev, 1942
Petrov, A.D.; Andreev, D.N., Synthesis of Monoalkylnaphthalenes and Their Hydro Derivatives, Zh. Obshch. Khim., 1942, 12, 95. [all data]

Klemm, Shabtai, et al., 1981
Klemm, L.H.; Shabtai, J.; Bodily, K.C., Gas chromatography of some C₁₃-C₁₆ alkylnaphthalenes on Bentone 34, silicone fluid DC 550 and Apiezon L phases, J. Chromatogr., 1981, 206, 2, 372-375, https://doi.org/10.1016/S0021-9673(00)82549-2 . [all data]

Engewald, Wennrich, et al., 1979
Engewald, W.; Wennrich, L.; Ritter, E., Molekülstruktur und Retentionsverhalten. XII. Zur Retention von Alkylnaphthalinen Bei der Gasverteilungs- und Gas-Adsorptions-Chromatographie, J. Chromatogr., 1979, 174, 2, 315-323, https://doi.org/10.1016/S0021-9673(00)86005-7 . [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔcH°liquid	Enthalpy of combustion of liquid at standard conditions
  ΔfH°liquid	Enthalpy of formation of liquid at standard conditions

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