Phenol, 3-methyl-

• Formula: C₇H₈O
• Molecular weight: 108.1378
• IUPAC Standard InChI: InChI=1S/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H3 Copy

  
• IUPAC Standard InChIKey: RLSSMJSEOOYNOY-UHFFFAOYSA-N Copy
• CAS Registry Number: 108-39-4
• Chemical structure:
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• Other names: m-Cresol; m-Cresole; m-Cresylic acid; m-Hydroxytoluene; m-Kresol; m-Methylphenol; m-Oxytoluene; m-Toluol; 1-Hydroxy-3-methylbenzene; 3-Cresol; 3-Hydroxytoluene; 3-Methylphenol; meta-Cresol; Cresol, meta; Rcra waste number U052; Cresol,m-; NSC 8768
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
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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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
BS - Robert L. Brown and Stephen E. Stein

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.

Cepeda, Gonzalez, et al., 1989
Cepeda, E.; Gonzalez, C.; Resa, J.M., Isobaric vapor-Liquid Equilibrium for the Cumene-Phenol System, J. Chem. Eng. Data, 1989, 34, 270. [all data]

Cepeda, Gonzalez, et al., 1989, 2
Cepeda, E.; Gonzalez, C.; Resa, J.M.; Ortiz de Salido, C., Isobaric Vapor-Liquid Equilibrium for the Cumene-m-Cresol and Phenol- m-Cresol Systems at 13.33 kPa, J. Chem. Eng. Data, 1989, 34, 429. [all data]

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]

von Terres, Gebert, et al., 1955
von Terres, E.; Gebert, F.; Hulsemann, H.; Petereit, H.; Toepsch, H.; Ruppert, W., Brennst.-Chem., 1955, 36, 272. [all data]

Tschamler and Krischai, 1951
Tschamler, H.; Krischai, H., Binary liquid mixtures: XV. Quinoline + m-cresol, a strongly neg. system, Monatsh. Chem., 1951, 82, 259. [all data]

Lecat, 1949
Lecat, M., Tables Azeotropiques, Vol. 1, 10th ed., Brussels, Belgium, 1949. [all data]

Pardee and Weinrich, 1944
Pardee, W.A.; Weinrich, W., Physical properties of alkylated phenols, Ind. Eng. Chem., 1944, 36, 595. [all data]

Lecat, 1943
Lecat, M., Azeotropes of Ethyl Urethane and other Azeotropes, C. R. Hebd. Seances Acad. Sci., 1943, 217, 273. [all data]

Timmermans and Hennaut-Roland, 1937
Timmermans, J.; Hennaut-Roland, M., Works from International Bureau at Physical-Chemical Standards. VIII. Physical constants of 20 organic compounds, J. Chim. Phys. Phys.-Chim. Biol., 1937, 34, 693. [all data]

Piatti, 1931
Piatti, L., Z. Phys. Chem., Abt. A, 1931, 152, 36. [all data]

Bhatnagar, Mathur, et al., 1930
Bhatnagar, S.S.; Mathur, R.N.; Mal, R.S., Philos. Mag., 1930, 10, 101. [all data]

Schoorl, 1929
Schoorl, N., The influence of position isomerism on some specific constants., Recl. Trav. Chim. Pays-Bas, 1929, 48, 935. [all data]

Kendall and Beaver, 1921
Kendall, J.; Beaver, J.J., Compound Formation in Phenol-cresol Mixtures, J. Am. Chem. Soc., 1921, 43, 1853. [all data]

Dawson and Mountford, 1918
Dawson, H.M.; Mountford, C.A., J. Chem. Soc., Trans., 1918, 113, 937. [all data]

Masse and Leroux, 1916
Masse, R.; Leroux, L., C. R. Hebd. Seances Acad. Sci., 1916, 163, 361. [all data]

Richards and Mathews, 1908
Richards, T.W.; Mathews, J.H., The Relation Between Compressibility, Surface Tension, and Other Properties of Material, J. Am. Chem. Soc., 1908, 30, 8-13. [all data]

Perkin, 1896
Perkin, W.H., LXIX. On Magnetic Rotatory Power, especially of Aromatic Compounds, J. Chem. Soc., 1896, 69, 1025-1257. [all data]

Pinette, 1888
Pinette, J., X boiling point and specific volume of a few phenols and phenol ethers, Justus Liebigs Ann. Chem., 1888, 243, 32. [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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