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:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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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 melting 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
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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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.

Inozemtsev, Liakumovich, et al., 1972
Inozemtsev, P.P.; Liakumovich, A.G.; Gracheva, Z.D., Russ. J. Phys. Chem., 1972, 46, 6, 914. [all data]

Jones and Noack, 1961
Jones, R.N.; Noack, K., Can. J. Chem., 1961, 39, 2214. [all data]

Azatyan, 1960
Azatyan, V.D., Izv. Akad. Nauk Arm. SSR, Khim. Nauki, 1960, 13, 2-3, 181. [all data]

Goldsmith, Schlatter, et al., 1958
Goldsmith, E.A.; Schlatter, M.J.; Toland, W.G., J. Org. Chem., 1958, 23, 1871. [all data]

Topchiev and Tumerman, 1958
Topchiev, A.V.; Tumerman, B.M., Tr. Mosk. Neft. Inst., 1958, No. 23, 9. [all data]

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

Bowman, Stevens, et al., 1957
Bowman, R.S.; Stevens, D.R.; Baldwin, W.E., J. Am. Chem. Soc., 1957, 79, 87. [all data]

Kolka, Napolitano, et al., 1957
Kolka, A.J.; Napolitano, J.P.; Filbey, A.H.; Ecke, G.G., J. Org. Chem., 1957, 22, 642. [all data]

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

Stroh, Seydel, et al., 1957
Stroh, R.; Seydel, R.; Hahn, W., Alkylation of phenols with olefins., Angew. Chem., 1957, 69, 699. [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]

Hofer and Peebles, 1955
Hofer; Peebles, Anal. Chem., 1955, 27, 1852. [all data]

Teuber and Staiger, 1955
Teuber; Staiger, Chem. Ber., 1955, 88, 802. [all data]

Berliner, Berliner, et al., 1954
Berliner, E.; Berliner, F.; Nelidow, I., J. Am. Chem. Soc., 1954, 76, 507. [all data]

Cullinane and Leyshon, 1954
Cullinane, N.M.; Leyshon, D.M., J. Chem. Soc., 1954, 1954, 2942. [all data]

Sidorova, 1952
Sidorova, N.G., Zh. Obshch. Khim., 1952, 22, 962. [all data]

Parker and Goldblatt, 1950
Parker, E.D.; Goldblatt, L.A., The Thermal Isomerization of alo-Ocimene, J. Am. Chem. Soc., 1950, 72, 2151-9. [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]

Dubinin, 1949
Dubinin, B.M., J. Gen. Chem. USSR (Engl. Transl.), 1949, 19, 663. [all data]

Sears and Kitchen, 1949
Sears, W.C.; Kitchen, L.J., Infrared Studies of Hindered Phenols, J. Am. Chem. Soc., 1949, 71, 4110. [all data]

Stull, 1947
Stull, D.R., Organic compounds, Ind. Eng. Chem., 1947, 39, 517. [all data]

Tambovtseva and Tsukervanik, 1945
Tambovtseva, V.; Tsukervanik, I.P., Zh. Obshch. Khim., 1945, 15, 820. [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]

Huston and Hsieh, 1936
Huston, R.C.; Hsieh, T.Y., Condensation of Aliphatic Alcohols with Aromatic Compounds in the Presence of ALuminum Chloride I., J. Am. Chem. Soc., 1936, 58, 439. [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]

Read and Miller, 1932
Read, R.R.; Miller, E., J. Am. Chem. Soc., 1932, 54, 1195. [all data]

Anderson, 1930
Anderson, C.T., J. Am. Chem. Soc., 1930, 52, 2296. [all data]

Meyer and Bernhauer, 1929
Meyer, H.; Bernhauer, K., Alkylation of aromatic compounds., Monatsh. Chem., 1929, 53-54, 721. [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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