Butanoic acid, 2,2-dimethyl-

• Formula: C₆H₁₂O₂
• Molecular weight: 116.1583
• IUPAC Standard InChI: InChI=1S/C6H12O2/c1-4-6(2,3)5(7)8/h4H2,1-3H3,(H,7,8) Copy

  
• IUPAC Standard InChIKey: VUAXHMVRKOTJKP-UHFFFAOYSA-N Copy
• CAS Registry Number: 595-37-9
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Butyric acid, 2,2-dimethyl-; α,α-Dimethylbutanoic acid; α,α-Dimethylbutyric acid; 2,2-Dimethylbutanoic acid; 2,2-Dimethylbutyric acid
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
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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.

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]

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]

Kwart and Miller, 1954
Kwart, H.; Miller, R.K., Allylic Rearrangement in the Reactions of 1-Chloro-3-methyl-2-butene; An Attempt at Total Synthesis of Geraniol, J. Am. Chem. Soc., 1954, 76, 5403. [all data]

Quilico and Cardani, 1953
Quilico; Cardani, Gazz. Chim. Ital., 1953, 83, 155. [all data]

Coffman and Roland, 1950
Coffman, D.D.; Roland, J.R., J. Am. Chem. Soc., 1950, 72, 3392. [all data]

Levina and Shusherina, 1950
Levina, R.Ya.; Shusherina, N.P., Synthesis of Hydrocarbons XII. Hydrobromides of Diene Hydrocarbons in the Synthesis of Olefinic and Parafinic Hydrocaarbons with Quaternary Carbon, Zh. Obshch. Khim., 1950, 20, 868. [all data]

Huston and Agett, 1941
Huston, R.C.; Agett, A.H., The reaction of ethylene oxide with grignard's reagent, J. Org. Chem., 1941, 6, 123-133. [all data]

Ruzicka and Peyer, 1935
Ruzicka, L.; Peyer, E., Helv. Chim. Acta, 1935, 18, 676. [all data]

Conant, Webb, et al., 1929
Conant, J.B.; Webb, C.N.; Mendum, W.C., Trimethylacetaldehyde and dimethylethylacetaldehyde, J. Am. Chem. Soc., 1929, 51, 1246. [all data]

Kishner, 1913
Kishner, N., Zh. Russ. Fiz.-Khim. O-va., Chast Khim., 1913, 45, 949. [all data]

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

Haller and Bauer, 1909
Haller, A.; Bauer, E., C. R. Hebd. Seances Acad. Sci., 1909, 148, 127. [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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