Naphthalene, decahydro-, trans-

• Formula: C₁₀H₁₈
• Molecular weight: 138.2499
• IUPAC Standard InChI: InChI=1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2/t9-,10- Copy

  
• IUPAC Standard InChIKey: NNBZCPXTIHJBJL-MGCOHNPYSA-N Copy
• CAS Registry Number: 493-02-7
• 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.
• Stereoisomers:
  • Naphthalene, decahydro-, cis-
  • Naphthalene, decahydro-
• Other names: trans-Bicyclo[4.4.0]Decane; trans-Decahydronaphthalene; trans-Decalin; trans-Perhydronaphthalene; Decahydronaphthalene, trans-; Decahydronaphthalene, (E)-; (E)-Decahydronaphthalene; t-Decalin; Bicyclo[4.4.0]decane, isomer # 1; trans-Decaline
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Normal boiling point

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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

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.

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Cooper, Crowne, et al., 1967
Cooper, A.R.; Crowne, C.W.P.; Farrell, P.G., Gas-Liquid Chromatographic Studies of Electron-Donor-Acceptor Systems, Trans. Faraday Soc., 1967, 63, 447. [all data]

Dauben and Tweit, 1954
Dauben; Tweit, J. Am. Chem. Soc., 1954, 76, 3197. [all data]

Anonymous, 1953
Anonymous, R., , Physical Properties of Chemical Substances, Dow Chemical Company, 1953. [all data]

Boord, Greenlee, et al., 1949
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Wt., Am. Pet. Inst. Res. Proj. 45, Eleventh Annu. Rep., Ohio State Univ., 1949. [all data]

Foehr and Fenske, 1949
Foehr, E.G.; Fenske, M.R., Magneto-optic Rotation of Hydrocarbons, Ind. Eng. Chem., 1949, 41, 1956. [all data]

Seyer and Mann, 1945
Seyer, W.F.; Mann, C.W., The Vapor Pressures of cis- and trans-Decahydronaphthalene, J. Am. Chem. Soc., 1945, 67, 328. [all data]

Rank, Scott, et al., 1942
Rank, D.H.; Scott, R.W.; Fenske, M.R., Qualitive and quantitative analysis of hydrocarbon mixtures, Anal. Chem., 1942, 14, 816. [all data]

Seyer and Walker, 1938
Seyer, W.F.; Walker, R.D., Physical chemical properties of cis- and trans-decahydronaphthalene, J. Am. Chem. Soc., 1938, 60, 2125-8. [all data]

Prokopetz, 1935
Prokopetz, E.I., Zh. Prikl. Khim. (Leningrad), 1935, 8, 1214. [all data]

Zelinskii and Turova-Pollyak, 1932
Zelinskii, N.D.; Turova-Pollyak, M.B., Chem. Ber., 1932, 65, 1299. [all data]

Zelinskii and Turova-Pollyak, 1929
Zelinskii, N.D.; Turova-Pollyak, M.B., Chem. Ber., 1929, 62, 1658. [all data]

Huckel, 1925
Huckel, W., Justus Liebigs Ann. Chem., 1925, 441, 1. [all data]

Huckel, 1925, 2
Huckel, W., Chem. Ber., 1925, 58, 1449. [all data]

Zelinskii and Turova-Pollyak, 1925
Zelinskii, N.D.; Turova-Pollyak, M.B., Chem. Ber., 1925, 58, 1292. [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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