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:
  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: 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 melting point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
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Normal melting 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 by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

Go To: Top, Normal melting point, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Meva'a and Lichanot, 1990
Meva'a, L.M.; Lichanot, A., Thermodynamic properties in condensed phase of ortho, meta and para fluorotoluene, cresol and toluidine, Thermochim. Acta, 1990, 158, 335. [all data]

Andon, Biddiscombe, et al., 1960
Andon, R.J.L.; Biddiscombe, D.P.; Cox, J.D.; Handley, R.; Harrop, D.; Herington, E.F.G.; Martin, J.F., 1009. Thermodynamic properties of organic oxygen compounds. Part I. Preparation and physical properties of pure phenol, cresols, and xylenols, J. Chem. Soc., 1960, 5246, https://doi.org/10.1039/jr9600005246 . [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]

Carney and Sanford, 1953
Carney, G.E.; Sanford, J.K., Anal. Chem., 1953, 25, 1417. [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]

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

Deffet, 1940
Deffet, L., Piezometric Research. Temperatures of Fusion and Transformation, Bull. Soc. Chim. Belg., 1940, 49, 223. [all data]

Deffet, 1938
Deffet, L., Bull. Soc. Chim. Belg., 1938, 47, 461. [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]

Carter and Jones, 1934
Carter, E.G.; Jones, D.C., An experimental test of the validity of antonow's rule, Trans. Faraday Soc., 1934, 30, 1027. [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]

Pushin and Sladovic, 1928
Pushin, N.A.; Sladovic, L., Equilibrium in the binary systems cresols-amines, J. Chem. Soc., 1928, 1928, 2474. [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]

Bramley, 1916
Bramley, A., The Studyu of Binary Mixtures. Part III. Freezing Point Curves, J. Chem. Soc., 1916, 109, 469. [all data]

Kendall, 1916
Kendall, J., The Addition Compounds of Phenols With Organic Acids, J. Am. Chem. Soc., 1916, 38, 1309-23. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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