Naphthalene, decahydro-2,6-dimethyl-

• Formula: C₁₂H₂₂
• Molecular weight: 166.3031
• IUPAC Standard InChI: InChI=1S/C12H22/c1-9-3-5-12-8-10(2)4-6-11(12)7-9/h9-12H,3-8H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: XNOHNIPVHGINQP-UHFFFAOYSA-N Copy
• CAS Registry Number: 1618-22-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • cis,cis,cis-Bicyclo[4.4.0]decane, 3,8-dimethyl
  • cis,cis,trans-Bicyclo[4.4.0]decane, 3,8-dimethyl
  • cis,trans,cis-Bicyclo[4.4.0]decane, 3,8-dimethyl
  • cis,trans,trans-Bicyclo[4.4.0]decane, 3,8-dimethyl
  • trans,trans,cis-Bicyclo[4.4.0]decane, 3,8-dimethyl
  • trans,trans,trans-Bicyclo[4.4.0]decane, 3,8-dimethyl
• Other names: Decahydro-2,6-dimethylnaphthalene; 2,6-Dimethyldecalin; 2,6-dimethyldecahydro-naphthalene
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
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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, temperature ramp

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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.

Tepe, Sokmen, et al., 2005
Tepe, B.; Sokmen, M.; Sokmen, A.; Daferera, D.; Polissiou, M., Antimicrobial and antioxidative activity of the essential oil and various extracts of Cyclotrichium origanifolium (Labill.) Manden. Scheng., J. Food Eng., 2005, 69, 3, 335-342, https://doi.org/10.1016/j.jfoodeng.2004.08.024 . [all data]

Notes

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