Naphthalene, decahydro-1,6-dimethyl-4-(1-methylethyl)-

• Formula: C₁₅H₂₈
• Molecular weight: 208.3828
• IUPAC Standard InChI: InChI=1S/C15H28/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h10-15H,5-9H2,1-4H3/t11?,12?,13-,14+,15-/m0/s1 Copy

  
• IUPAC Standard InChIKey: FZZNNPQZDRVKLU-PCGVCOGMSA-N Copy
• CAS Registry Number: 29788-41-8
• 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:
  • Muurolane-c
  • Muurolane-d
• Stereoisomers:
  • Amorphane
  • Cadinane
  • Cadinane-a
  • Cadinane-b
  • Amorphane-a (isocadinane)
  • Cadinane-c
  • Muurolane-B
  • Amorphane-b
• Other names: Muurolane; 4-Isopropyl-1,6-dimethyldecahydronaphthalene; Naphthalene, decahydro-4-isopropyl-1,6-dimethyl-; Muurolane-a
• Information on this page:
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
• Options:
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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, 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.

Maarse, 1975
Maarse, H., Hydrogenolysis of terpenes in the injection port of a gas chromatograph. II. Sesquiterpenes, J. Chromatogr., 1975, 106, 2, 369-384, https://doi.org/10.1016/S0021-9673(00)93846-9 . [all data]

Andersen and Falcone, 1969
Andersen, N.H.; Falcone, M.S., The identification of sesquiterpene hydrocarbons from gas-liquid chromatography retention data, J. Chromatogr., 1969, 44, 52-59, https://doi.org/10.1016/S0021-9673(01)92497-5 . [all data]

Notes

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