1-Butene, 3-methyl-

• Formula: C₅H₁₀
• Molecular weight: 70.1329
• IUPAC Standard InChI: InChI=1S/C5H10/c1-4-5(2)3/h4-5H,1H2,2-3H3 Copy

  
• IUPAC Standard InChIKey: YHQXBTXEYZIYOV-UHFFFAOYSA-N Copy
• CAS Registry Number: 563-45-1
• 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: Isopropylethylene; α-Isoamylene; Vinylisopropyl; 2-Methyl-3-butene; 3-Methyl-1-butene; (CH3)2CHCH=CH2; Isopentene; UN 2371; UN 2561; 3-Methylbutene-1; 3-methylbut-1-ene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
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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.

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]

Schulte-Elte, Gadola, et al., 1971
Schulte-Elte, K.H.; Gadola, M.; Ohloff, G., Thermal Rearrangement of (+)-Isopinocampheol and (-)-Isopinocamphon, Helv. Chim. Acta, 1971, 54, 1813-22. [all data]

Eidus, Nuzitskii, et al., 1970
Eidus, Y.T.; Nuzitskii, K.V.; Yung-ping, Y., Carbonylation of Pentene-1 and 3-Methylbutehe-1- by Carbon Monoxide in the Presence of Hydrates of Boron Trifluoride, Izvest. Akad. Nauk SSSR, Ser. Khim., 1970, No. 7, 1673-5. [all data]

Gorin, Galkina, et al., 1966
Gorin, Yu.A.; Galkina, G.I.; Makashina, A.N.; Andreeva, N.P., Catalytic Dehydrogenation of Normal Pentenes and Isopentenes and of Their Mixtures, Diluted with Steam, Zh. Prikl. Khim., 1966, 39, 1577-83. [all data]

Kaal. T.A., Ordyan, et al., 1965
Kaal. T.A.; Ordyan, M.B.; Eidus, Y.T., Synthesis of Carboxylic Acid Derivatives Uner Conditions of Acid Catalysis From Carbon Monoxide, Olefines, and Acylating Agents, Zh. Org. Khim., 1965, 1, 1187-9. [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]

Thornton and Herald, 1948
Thornton, V.; Herald, A.E., Anal. Chem., 1948, 20, 9. [all data]

Tyazhelova, 1948
Tyazhelova, A.A., Monoethers of isopropyl- and trimethylethylene glycols., J. Gen. Chem. USSR (Engl. Transl.), 1948, 18, 449. [all data]

Anonymous, 1947
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1947. [all data]

Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]

Gerding and van der Vet, 1946
Gerding, H.; van der Vet, A.P., Raman spectra of the seven isomeric pentenes and quantitative analysis of two mixtures by means of the Raman effect, Recl. Trav. Chim. Pays-Bas, 1946, 64, 257. [all data]

Morrell, Paltz, et al., 1946
Morrell, C.E.; Paltz, W.J.; Packie, J.W.; Asbury, W.C.; Brown, C.L., Trans. Am. Inst. Chem. Eng., 1946, 42, 473. [all data]

Roy, 1946
Roy, A.N., Formation of Olefin Isomers in the Catalytic Dehydrogenation of Butyl [and sec-butyl] ande Isoamyl Alcohols, Proc. Natl. Acad. Sci., India, Sect. A, 1946, 12, 137-41. [all data]

Ewell and Hardy, 1941
Ewell, R.H.; Hardy, P.E., Isomerization Equilibria among the Branched Chain Pentenes, J. Am. Chem. Soc., 1941, 63, 3460. [all data]

Dolliver, Gresham, et al., 1937
Dolliver, M.A.; Gresham, T.L.; Kistiakowsky, G.B.; Vaughan, W.E., Heats of organic reactions: V heats of hydrogenation of various hydrocarbons, J. Am. Chem. Soc., 1937, 59, 831. [all data]

Carr and Walter, 1936
Carr, E.P.; Walter, G.F., The Ultraviolet Absorption SPectra of Simple Hydrocarbons II. In Liquid and Solution Phase, J. Chem. Phys., 1936, 4, 756. [all data]

Gredy, 1935
Gredy, B., Raman effect of organic chemicals a study of isopropylacetylene, isopropylethylene and of some of their derivatives, Bull. Soc. Chim. Fr., 1935, 2, 1951. [all data]

Davis, Thomson, et al., 1932
Davis, H.S.; Thomson, G.; Crandall, G.S., The role of liquid stationary films in batch absorption of gases: III rates of hydrogen absorption and relative rates of catalytic hydrogenation in alcohol, J. Am. Chem. Soc., 1932, 54, 2340. [all data]

Hyman and Wagner, 1930
Hyman, J.; Wagner, C.R., Autoxidation of the Amylenes, J. Am. Chem. Soc., 1930, 52, 4345. [all data]

Norris and Joubert, 1927
Norris, J.F.; Joubert, J.M., The Polymerization of teh Amylenes, J. Am. Chem. Soc., 1927, 49, 873. [all data]

Norris and Reuter, 1927
Norris, J.F.; Reuter, R., The rearrangement of isopropylethylene to trimethylethylene and the pyrogenic decomposition of pentene-2 and trimethylethylene, J. Am. Chem. Soc., 1927, 49, 2624-40. [all data]

Lagerlof, 1918
Lagerlof, D., Thermodynamic research: reduced formulas for simplified calculations of latent molar heat of evaporation, J. Prakt. Chem., 1918, 98, 136. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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