Phenol, p-tert-butyl-

• Formula: C₁₀H₁₄O
• Molecular weight: 150.2176
• IUPAC Standard InChI: InChI=1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3 Copy

  
• IUPAC Standard InChIKey: QHPQWRBYOIRBIT-UHFFFAOYSA-N Copy
• CAS Registry Number: 98-54-4
• Chemical structure:
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• Other names: Phenol, 4-(1,1-dimethylethyl)-; p-tert-Butylphenol; Butylphen; 4-tert-Butylphenol; 4-t-Butylphenol; 4-(1,1-Dimethylethyl)phenol; p-terc.Butylfenol; 1-Hydroxy-4-tert-butylbenzene; PTBP; Phenol, 4-tert-butyl-; p-t-Butylphenol; NSC 3697
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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
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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.

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [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]

Belorossova and Farberov, 1957
Belorossova, A.G.; Farberov, M.I., Uch. Zap. Yarosl. Tekhnol. Inst., 1957, 2, 21. [all data]

Loev and Massengale, 1957
Loev, B.; Massengale, J.T., J. Org. Chem., 1957, 22, 988. [all data]

Burton, Munday, et al., 1956
Burton, H.B.; Munday, D.A.; Praill, P.F.G., J. Chem. Soc., 1956, 1956, 3933. [all data]

Dreisbach and Martin, 1949
Dreisbach, R.R.; Martin, R.A., Physical Data on Some Organic Compounds, Ind. Eng. Chem., 1949, 41, 2875-8. [all data]

Mckenna and Sowa, 1938
Mckenna, J.F.; Sowa, F.J., Organic Reactions with Boron Trifluoride XVII, J. Am. Chem. Soc., 1938, 60, 124. [all data]

Simons, Archer, et al., 1938
Simons, J.H.; Archer, S.; Passinio, H.J., Hydrogen Fluiride as a Condensing Agent V. Reactions of Compounds Containing Oxygen and Reactions of Tertiary Halides with Olefins, J. Am. Chem. Soc., 1938, 60, 2956. [all data]

Natelson, 1934
Natelson, S., Rearrangement of Alkyl Phenyl Ethers on Heating at Moderate Temp. Synthesis of Tertiary Amyl, Tertiary Butyl and Diisobutyl Phenols, J. Am. Chem. Soc., 1934, 56, 1583. [all data]

Smith, 1933
Smith, R.A., Studies in the Rearrangements of Phenyl Ethers. The Action of Aluminum Chloride on Butyl Phenyl Ethers, J. Am. Chem. Soc., 1933, 55, 3718. [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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