2,2-Dimethylbutanedioic acid

• Formula: C₆H₁₀O₄
• Molecular weight: 146.1412
• IUPAC Standard InChI: InChI=1S/C6H10O4/c1-6(2,5(9)10)3-4(7)8/h3H2,1-2H3,(H,7,8)(H,9,10) Copy

  
• IUPAC Standard InChIKey: GOHPTLYPQCTZSE-UHFFFAOYSA-N Copy
• CAS Registry Number: 597-43-3
• 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: 2,2-Dimethylsuccinic acid; Butanedioic acid, 2,2-dimethyl-; Succinic acid, 2,2-dimethyl-
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Reaction thermochemistry data
  • IR Spectrum
  • Mass spectrum (electron ionization)
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Phase change data

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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

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Sisido, Kazama, et al., 1959
Sisido, K.; Kazama, Y.; Kodama, H.; Nozaki, H., J. Am. Chem. Soc., 1959, 81, 5817. [all data]

Chel'tsova, Chernyshev, et al., 1955
Chel'tsova, M.A.; Chernyshev, E.A.; Petrov, A.D., Behaviour of Alkenyl Halides with Unsaturated Bond in γ-, δ, ε-Postion in Condenstation Reactions with Alkyl Halides in the Presence of Magnesium, Izv. Akad. Nauk SSSR, 1955, 1955, 522-7. [all data]

Finch, Furman, et al., 1951
Finch, H.; Furman, K.E.; Ballard, S.A., The Alkaline Cleavage of Isophorone, J. Am. Chem. Soc., 1951, 73, 4299. [all data]

Henne and Chanan, 1944
Henne, A.L.; Chanan, H.H., Diolefins from Allylic Chlorides II., J. Am. Chem. Soc., 1944, 66, 392. [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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