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
  The 3d structure may be viewed using Java or Javascript.
• 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
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• 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
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
  • Switch to calorie-based units

Data at NIST subscription sites:

• 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 melting 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 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

Go To: Top, Normal melting point, References

• Symbols used in this document:
  

  Tfus	Fusion (melting) 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.