Naphthalene, 2-ethyl-

• Formula: C₁₂H₁₂
• Molecular weight: 156.2237
• IUPAC Standard InChI: InChI=1S/C12H12/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h3-9H,2H2,1H3 Copy

  
• IUPAC Standard InChIKey: RJTJVVYSTUQWNI-UHFFFAOYSA-N Copy
• CAS Registry Number: 939-27-5
• 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: β-Ethylnaphthalene; 2-Ethylnaphthalene
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• Information on this page:
  • Phase change data
  • IR Spectrum
  • UV/Visible spectrum
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of vaporization

IR Spectrum

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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

Gas Phase Spectrum

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Additional Data

UV/Visible spectrum

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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: Victor Talrose, Eugeny B. Stern, Antonina A. Goncharova, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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Additional Data

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.

Kochetkov, Nifant'ev, et al., 1957
Kochetkov, N.K.; Nifant'ev, E.E.; Nesmeyanov, A.N., Cyclic Acetals of β-Oxoaldehydes and Their Use in Synthesis of Alkylnaphthalenes, Izv. Akad. Nauk S.S.S.R., 1957, 1957, 949-55. [all data]

Adkins and Davis, 1949
Adkins, H.; Davis, J.W., Catalytic Dehydrogenation of Hydroaromatic Compounds in Benzene II., J. Am. Chem. Soc., 1949, 71, 2955. [all data]

Koelbel, 1949
Koelbel, H., Alkylnaphthalenes as Lubricating-oil Models, Brennst.-Chem., 1949, 30, 73-80. [all data]

Lei, Chankalal, et al., 2002
Lei, Ying Duan; Chankalal, Raymond; Chan, Anita; Wania, Frank, Supercooled Liquid Vapor Pressures of the Polycyclic Aromatic Hydrocarbons, J. Chem. Eng. Data, 2002, 47, 4, 801-806, https://doi.org/10.1021/je0155148 . [all data]

Sasse, Jose, et al., 1988
Sasse, Karim; Jose, Jacques; Merlin, Jean-Claude, A static apparatus for measurement of low vapor pressures. Experimental results on high molecular-weight hydrocarbons, Fluid Phase Equilibria, 1988, 42, 287-304, https://doi.org/10.1016/0378-3812(88)80065-7 . [all data]

Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw, Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2 . [all data]

Ramart-Lucas, 1950
Ramart-Lucas, P., Introduction a l'etude du comportement spectral des combinaisons polynucleaires, Bull. Soc. Chim. Fr., 1950, 17, 259-265. [all data]

Notes

Go To: Top, Phase change data, IR Spectrum, UV/Visible spectrum, References

• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔvapH	Enthalpy of vaporization

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