1-Butyne, 3,3-dimethyl-

• Formula: C₆H₁₀
• Molecular weight: 82.1436
• IUPAC Standard InChI: InChI=1S/C6H10/c1-5-6(2,3)4/h1H,2-4H3 Copy

  
• IUPAC Standard InChIKey: PPWNCLVNXGCGAF-UHFFFAOYSA-N Copy
• CAS Registry Number: 917-92-0
• 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: t-Butylacetylene; tert-Butylacetylene; 3,3-Dimethyl-1-Butyne; 3,3-Dimethylbutyne; 3,3,3-Trimethylpropyne; (CH3)3CC≡CH; 3,3-Dimethylbutyne-1
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
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  • IR Spectrum
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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.

Farchan Laboratories, 1990
Farchan Laboratories, Research Chemicals Catalog, Farchan Laboratories, Gainesville, FL, 1990, 91. [all data]

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]

Pimenova, Kozina, et al., 1986
Pimenova, S.M.; Kozina, M.P.; Gal'chenko, G.L.; Siretskaya, T.V.; Takhistov, V.V.; Kuznetsova, T.S.; Proskurnina, M.V.; Kotel'nikova, T.A., Heats of combustion and formation of some compounds with acetylene binding, Termodin. Org. Soedin., 1986, 1986, 12. [all data]

Hatch, Weiss, et al., 1961
Hatch, L.F.; Weiss, H.D.; Li, T.P., Allylic Chlorides XXVI. 1-Chloro-2-heptenes and 1-Chloro-4,4-dimethyl-2-pentenes, J. Org. Chem., 1961, 26, 61-5. [all data]

Heilmann, de Gaudemaris, et al., 1957
Heilmann; de Gaudemaris, G.; Arnaud, Bull. Soc. Chim. Fr., 1957, 1957, 112. [all data]

Wotiz, Hollingsworth, et al., 1955
Wotiz, J.H.; Hollingsworth, C.A.; Dessy, R.E., J. Org. Chem., 1955, 20, 1544. [all data]

Miller, Greenlee, et al., 1954
Miller, H.M.; Greenlee, K.W.; Derfer, J.M.; Boord, C.E., J. Org. Chem., 1954, 19, 1882. [all data]

Pomerantz, Fookson, et al., 1954
Pomerantz, P.; Fookson, A.; Mears, T.W.; Rothberg, S.; Howard, F.L., Synthesis and Physical Properties of Several Acetylenic Hydrocarbons, J. Res. Natl. Bur. Stand. (U. S.), 1954, 52, 51. [all data]

Schlubach and Franzen, 1953
Schlubach; Franzen, Justus Liebigs Ann. Chem., 1953, 583, 93. [all data]

Zakharova, 1951
Zakharova, A.I., Zh. Obshch. Khim., 1951, 21, 493. [all data]

Cleveland and Murray, 1943
Cleveland, F.F.; Murray, M.J., Raman spectra of acetylenes: vii. symmetrical top acetylenes., J. Chem. Phys., 1943, 11, 450. [all data]

Krestinskii and Kelbovskaya, 1935
Krestinskii, V.N.; Kelbovskaya, M.K., Chem. Ber., 1935, 68, 512. [all data]

Willemart, 1935
Willemart, A., Bull. Soc. Chim. Fr., 1935, 2, 867. [all data]

Johnson and McEwen, 1926
Johnson, J.R.; McEwen, W.L., The Identification of Monosubstituted Acetylenes. Derivatives of Diethinyl Mercury, J. Am. Chem. Soc., 1926, 48, 469. [all data]

De Graef, 1925
De Graef, H., Trimethylpropylmethane and Methylethylpropyllmethane, Bull. Soc. Chim. Belg., 1925, 34, 427. [all data]

Ivitskii, 1924
Ivitskii, P., Bull. Soc. Chim. Fr., 1924, 35, 357. [all data]

Pariselle, 1923
Pariselle, M., Pinenes, Ann. Chim. (Paris), 1923, 19, 119-35. [all data]

Timmermans, 1922
Timmermans, J., Investigation of the Freezing Point of Organic Substances VII, Bull. Soc. Chim. Belg., 1922, 31, 389. [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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