Naphthalene, decahydro-2-methyl-

• Formula: C₁₁H₂₀
• Molecular weight: 152.2765
• IUPAC Standard InChI: InChI=1S/C11H20/c1-9-6-7-10-4-2-3-5-11(10)8-9/h9-11H,2-8H2,1H3 Copy

  
• IUPAC Standard InChIKey: GREARFRXIFVLGB-UHFFFAOYSA-N Copy
• CAS Registry Number: 2958-76-1
• 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.
• Species with the same structure:
  • trans-Decalin, 2-methyl-
  • cis-Decalin, 2-syn-methyl-
• Stereoisomers:
  • trans-Decalin, 2a-methyl
  • trans-Decalin, 2e-methyl
  • 2-Methyldecalin, cis
  • cis,cis-Bicyclo[4.4.0]decane, 3-methyl
  • cis,trans-Bicyclo[4.4.0]decane, 3-methyl
  • trans,cis-Bicyclo[4.4.0]decane, 3-methyl
  • trans,trans-Bicyclo[4.4.0]decane, 3-methyl
• Other names: Decahydro-2-methylnaphthalene; 2-Methyldecalin; Decahydronaphthalene, 2-methyl; 2-Methyldecalin, isomer 4; 2-Methyldecahydronaphthalene; 2-Methyldecalin, isomer 1; 2-Methyldecalin, isomer 2; 2-Methyldecalin, isomer 3
• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Mass spectrum (electron ionization)
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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 by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

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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Kovats' RI, non-polar column, temperature ramp

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Van Den Dool and Kratz RI, non-polar column, custom temperature program

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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.

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]

Weissenberger, Henke, et al., 1926
Weissenberger, G.; Henke, R.; Katschinka, H., Binary liquid mixtures: xx systems with substituting hydronaphthalenes, Z. Anorg. Allg. Chem., 1926, 153, 33. [all data]

Litvinenko, Isakova, et al., 1988
Litvinenko, G.S.; Isakova, L.A.; Rubanyk, N.N., Quantitative correlation between structure of stereoisomeric saturated cyclic compounds and gas-chromatographic retention indices. I. Methysubstituted, Izv. AN Kaz. SSR, Ser. Khim., 1988, 5, 54-66. [all data]

Bredael, 1982
Bredael, P., Retention indices of hydrocarbons on SE-30, J. Hi. Res. Chromatogr. Chromatogr. Comm., 1982, 5, 6, 325-328, https://doi.org/10.1002/jhrc.1240050610 . [all data]

Rembold, Wallner, et al., 1989
Rembold, H.; Wallner, P.; Nitz, S.; Kollmannsberger, H.; Drawert, F., Volatile components of chickpea (Cicer arietinum L.) seed, J. Agric. Food Chem., 1989, 37, 3, 659-662, https://doi.org/10.1021/jf00087a018 . [all data]

Selli, Rannou, et al., 2006
Selli, S.; Rannou, C.; Prost, C.; Robin, J.; Serot, T., Characterization of Aroma-Active Compounds in Rainbow Trout (Oncorhynchus mykiss) Eliciting an Off-Odor, J. Agric. Food Chem., 2006, 54, 25, 9496-9502, https://doi.org/10.1021/jf0619582 . [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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