Propanoic acid, 2,2-dimethyl-

• Formula: C₅H₁₀O₂
• Molecular weight: 102.1317
• IUPAC Standard InChI: InChI=1S/C5H10O2/c1-5(2,3)4(6)7/h1-3H3,(H,6,7) Copy

  
• IUPAC Standard InChIKey: IUGYQRQAERSCNH-UHFFFAOYSA-N Copy
• CAS Registry Number: 75-98-9
• 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: Pivalic acid; α,α-Dimethylpropionic acid; tert-Pentanoic acid; Neopentanoic acid; Trimethylacetic acid; 2,2-Dimethylpropanoic acid; 2,2-Dimethylpropionic acid; tert-C4H9COOH; Acetic acid, trimethyl-; Propionic acid, 2,2-dimethyl-; Kyselina 2,2-dimethylpropionova; Kyselina pivalova; NSC 65449; Neovaleric acid; Versatic 5
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • 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)
  • Gas Chromatography
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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

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.

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]

Frinton Laboratories Inc., 1986
Frinton Laboratories Inc., Catalog Number 11, Frinton Laboratories Inc., Vineland, NJ, 1986, 99. [all data]

Eidus, Puzitskii, et al., 1960
Eidus, Y.T.; Puzitskii, K.V.; Sterligov, O.D., Synthesis of Esters and Other Derivatives of Carboxylic Acis by Acid Catalysis from Carbon Monoxide, Olefins, and Acylating Compounds, Zh. Obshch. Khim., 1960, 30, 3799-3802. [all data]

Landis and Hamilton, 1960
Landis, P.S.; Hamilton, L.A., J. Org. Chem., 1960, 25, 1742. [all data]

Brandstrom, 1959
Brandstrom, A., Acta Chem. Scand., 1959, 13, 610. [all data]

Szmant and Emerson, 1956
Szmant, H.H.; Emerson, W., The Grignard Reaction and Infrared SPectra of Cyclic Sulfites, J. Am. Chem. Soc., 1956, 78, 454. [all data]

Yohe, Dunbar, et al., 1956
Yohe, G.R.; Dunbar, J.E.; Pedrotti, R.L.; Scheidt, F.M.; Lee, F.G.H.; Smith, E.C., J. Org. Chem., 1956, 21, 1289. [all data]

Bartlett and Stiles, 1955
Bartlett, P.D.; Stiles, M., Highly branched molecules: IV solvolysis of the p-nitrobenzoate of tri-t- butylcarbinol and some of its homologs, J. Am. Chem. Soc., 1955, 77, 2806. [all data]

Archer and Hickinbottom, 1954
Archer, D.P.; Hickinbottom, W.J., The synthesis and reactions of branched-chain hydrocarbons: V oxidation of 2,2,4-trimethylpentane and of 2,2,4,6,6-pentamethylheptane by chromic oxide, J. Chem. Soc., 1954, 1954, 4197. [all data]

Hancock, Watson, et al., 1954
Hancock, C.K.; Watson, G.M.; Gilby, R.F., Heats of Combustion of Five-Carbon Fatty Acids and Their Methyl and Ethyl Esters, J. Phys. Chem., 1954, 58, 127. [all data]

James and Martin, 1952
James, A.T.; Martin, A.J.P., Biochem. J., 1952, 50, 679. [all data]

Meshcheryakov and Petrova, 1952
Meshcheryakov, A.P.; Petrova, L.V., Trimethylacetic Acid, Akad NAuk S.S.S.R., Inst. Org. Khim., Sintesy Org. Soedinenii, Sbornik, 1952, 2, 132-3. [all data]

Nametkin and Zabrodina, 1951
Nametkin, S.S.; Zabrodina, K.S., Dokl. Akad. Nauk SSSR, 1951, 75, 543. [all data]

Spindt, Stevens, et al., 1951
Spindt, R.S.; Stevens, D.R.; Baldwin, W.E., J. Am. Chem. Soc., 1951, 73, 3693. [all data]

Heintzeler, 1950
Heintzeler, M., Justus Liebigs Ann. Chem., 1950, 569, 102. [all data]

Partridge and Garrison, 1950
Partridge, W.S.; Garrison, J. Am. Chem. Soc., 1950, 72, 4302. [all data]

Mosher and Whitmore, 1948
Mosher, W.A.; Whitmore, F.C., J. Am. Chem. Soc., 1948, 70, 2544. [all data]

Schmerling, 1948
Schmerling, L., Condensation of Saturted Hydrocarbons with Haloolefins II. The Reaction of Isobutane with cis- and trans-Dichloroethylene, J. Am. Chem. Soc., 1948, 70, 379-81. [all data]

Pohl, Hobbs, et al., 1941
Pohl, H.A.; Hobbs, M.E.; Gross, P.M., Electric polarization of carboxylic acids in dilute solutions of nonpolar solvents: I the relation of electric polarization to the association of carboxylic acids in hydrocarbon solvents, J. Chem. Phys., 1941, 9, 408. [all data]

Venus-Danilova, 1941
Venus-Danilova, E.D., Zh. Obshch. Khim., 1941, 11, 847. [all data]

Whitmore, Wilson, et al., 1941
Whitmore, F.C.; Wilson, C.D.; Capinjola, J.V.; Tongberg, C.O.; Fleming, G.H.; McGrew, R.V.; Cosby, J.N., J. Am. Chem. Soc., 1941, 63, 2035. [all data]

Magnani and McElvain, 1938
Magnani, A.; McElvain, S.M., The reaction of various alkyl benzoates with sodium alkoxides., J. Am. Chem. Soc., 1938, 60, 813. [all data]

Kohlraush, Koppl, et al., 1933
Kohlraush, K.W.F.; Koppl, F.; Pongratz, A., Z. Phys. Chem., Abt. B, 1933, 21, 242. [all data]

Puntambeker and Zoellner, 1932
Puntambeker, S.V.; Zoellner, E.A., Organic Synthesis, Collective Volume 1, Willey-Intersci- ence: New York, pp 524-8, 1932. [all data]

Fomin and Sochanski, 1913
Fomin, W.; Sochanski, N., Chem. Ber., 1913, 46, 244. [all data]

Richard, 1910
Richard, A., Ann. Chim. Phys., 1910, 21, 323. [all data]

Bistrzycki and Mauron, 1907
Bistrzycki, A.; Mauron, Chem. Ber., 1907, 40, 4370. [all data]

Pomeranz, 1897
Pomeranz, Monatsh. Chem., 1897, 18, 575. [all data]

Tissier, 1893
Tissier, L., Ann. Chim. Phys., 1893, 29, 321. [all data]

Butlerov, 1874
Butlerov, A., Justus Liebigs Ann. Chem., 1874, 173, 355. [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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