Naphthalene, 2-methyl-

• Formula: C₁₁H₁₀
• Molecular weight: 142.1971
• IUPAC Standard InChI: InChI=1S/C11H10/c1-9-6-7-10-4-2-3-5-11(10)8-9/h2-8H,1H3 Copy

  
• IUPAC Standard InChIKey: QIMMUPPBPVKWKM-UHFFFAOYSA-N Copy
• CAS Registry Number: 91-57-6
• 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.
• Other names: β-Methylnaphthalene; 2-Methylnaphthalene; 2-methyInaphthalene; Methyl-2-naphthalene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
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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

Go To: Top, Normal boiling point, Notes

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]

Anderson, Smith, et al., 1953
Anderson, D.G.; Smith, J.C.; Rallings, R.J., J. Chem. Soc., 1953, 1953, 443. [all data]

Anonymous, 1952
Anonymous, R., , Physical Properties of Chemical Substances, Dow Chemical Co., 1952. [all data]

Kinney and Pincus, 1951
Kinney, C.R.; Pincus, I., Catalytic Air Oxidation of Higher Aromatics to Phthalic Anhydride, Ind. Eng. Chem., 1951, 43, 2880. [all data]

Bailey, Pickering, et al., 1949
Bailey, A.S.; Pickering, G.B.; Smith, J.C., Alkylnaphthalenes: III the n-butyl, amyl, and hexylnaphthalenes, J. Inst. Pet., 1949, 35, 103-17. [all data]

Othmer, Savitt, et al., 1949
Othmer, D.F.; Savitt, S.A.; Krasner, A.; Goldberg, A.M.; Markowitz, D., Composition of vapors from boiling binary solutions. Systems with m- or p-cresol as one component., Ind. Eng. Chem., 1949, 41, 572. [all data]

Anderson, 1948
Anderson, J.A., Determination of Naphthalene, Methylnaphthalenes, and Total Naphthalenes in Admixture with Other Hydrocarbons by Ultraviolet Absorption, Proc. Am. Pet. Inst., Sect. 3, 1948, 28, 81-4. [all data]

Cleaves, Carver, et al., 1948
Cleaves, A.P.; Carver, M.S.; Hibbard, R.R., , Natl. Advis. Comm. Aeronaut., 1948. [all data]

Cullinane and Chard, 1948
Cullinane, N.M.; Chard, S.J., Action of Methanol on Naphthalene in the Presence of Catalysts of the Auliman-silica Type. Formation of 2-Methylnaphthalene, J. Chem. Soc., 1948, 1948, 804. [all data]

Morrell, Pickering, et al., 1948
Morrell, S.H.; Pickering, G.B.; Smith, J.C., Alkylnaphthalenes II. The Methyl-, Ethyl-, and Propylnaphthalenes, J. Inst. Pet., 1948, 34, 677. [all data]

Lecat, 1947
Lecat, M., Some azeotropes of which one constituant is heterocyclic nitrogen, Ann. Soc. Sci. Bruxelles, Ser. 1, 1947, 61, 73. [all data]

Rossini and Mair, 1941
Rossini, F.D.; Mair, B.J., Proc., Am. Pet. Inst., Sect. 3, 1941, 22, 7. [all data]

Mair and Streiff, 1940
Mair, B.J.; Streiff, A.J., Separation of the aromatic hydrocarbons, and the isolation of n-dodecane, naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene from the kerosene fraction of petroleum, J. Res. Natl. Bur. Stand. (U. S.), 1940, 24, 395-414. [all data]

Roux, 1887
Roux, L., Ann. Chim. Phys., 1887, 12, 289. [all data]

Schulze, 1884
Schulze, K.E., Chem. Ber., 1884, 17, 842. [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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