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
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• 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
  • Henry's Law data
  • Gas phase ion energetics data
  • Ion clustering data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
  • Switch to SI units

Data at NIST subscription sites:

• NIST / TRC Web Thermo Tables, "lite" edition (thermophysical and thermochemical data)
• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Normal boiling point

Go To: Top, References, Notes

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

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.

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

Go To: Top, Normal boiling point, References

• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.