1-Pentene, 2-methyl-

• Formula: C₆H₁₂
• Molecular weight: 84.1595
• IUPAC Standard InChI: InChI=1S/C6H12/c1-4-5-6(2)3/h2,4-5H2,1,3H3 Copy

  
• IUPAC Standard InChIKey: WWUVJRULCWHUSA-UHFFFAOYSA-N Copy
• CAS Registry Number: 763-29-1
• 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: 2-Methyl-1-pentene; 4-Methyl-4-pentene; C2H5CH2C(CH3)=CH2; 2-Methylpentene; 2-Methyl-pentene-1; 2-methylpent-1-ene
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
  • Switch to calorie-based units

Data at NIST subscription sites:

• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Normal boiling point

Go To: Top, References, Notes

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]

Parnes, Khotimskaya, et al., 1969
Parnes, Z.N.; Khotimskaya, G.A.; Kudryavtsev, R.V.; Lukina, M.Y.; Kursanov, D.N., The Behavior of Cyclopropane Hydrocarbons in Ionic Hydrogenation Reactions, Dokl. Akad. Nauk SSSR, Ser. Khim., 1969, 184, 615-8. [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]

Kryukov and Farberov, 1962
Kryukov, S.I.; Farberov, M.I., Syntheses based on 2-methyl-1-pentene., Zh. Prikl. Khim., 1962, 35, 2319-24. [all data]

Wright, 1961
Wright, F.J., Influence of temperature on viscosity of nonassociated liquids, J. Chem. Eng. Data, 1961, 6, 454. [all data]

Wright, 1960
Wright, F.J., Latent Heat of Vaporization and Composition, Recl. Trav. Chim. Pays-Bas, 1960, 79, 784-9. [all data]

Schuhmacher, Wibaut, et al., 1953
Schuhmacher, J.P.; Wibaut, J.P.; Paerels, G.B., Recl. Trav. Chim. Pays-Bas, 1953, 72, 1037. [all data]

Kelso, Greenlee, et al., 1952
Kelso, R.G.; Greenlee, K.W.; Derfer, J.M.; Boord, C.E., The Synthesis and Properties of 1,1,2-Trimethylcyclopropane, J. Am. Chem. Soc., 1952, 74, 287-92. [all data]

Anonymous, 1951
Anonymous, R., , Sunbury Rep. No. 4199, Anglo-Iranian Oil Co., 1951. [all data]

Braun, Spooner, et al., 1950
Braun, W.G.; Spooner, D.F.; Fenske, M.R., Raman spectra hydrocarbons and oxygenated compounds, Anal. Chem., 1950, 22, 1074. [all data]

Koch, 1948
Koch, H., , Unpublished, Kaiser-Wilhelm Inst. Mulheim, Ruhr, Germany, 1948. [all data]

Kozlov, 1948
Kozlov, N.S., The Boiling Points of Compounds of the Aliphatic Series, Neft. Khoz., 1948, 1948, No. 4, 47. [all data]

Spengler, 1948
Spengler, G., Unpublished, Inst. Kohleforschung, Prague, Czechosl- ovakia (transmitted by L. L. Newman, U. S, 1948. [all data]

Boord, 1942
Boord, C.E., Oil & Gas J., 1942, 41, 27, 188. [all data]

Goldwasser and Taylor, 1939
Goldwasser, S.; Taylor, H.S., Catalytic dehydration of c6-c8 aliphatic alcohols, J. Am. Chem. Soc., 1939, 61, 1751. [all data]

Schmitt and Boord, 1932
Schmitt, C.G.; Boord, C.E., Nuclear syntheses in the olefin series: III the hexenes, J. Am. Chem. Soc., 1932, 54, 751-61. [all data]

Brooks and Humphrey, 1918
Brooks, B.T.; Humphrey, I., The Action of Concentrated Sulfuric Acid on Olefins, with Particular Reference to the Refining of Petroleum Distillates, J. Am. Chem. Soc., 1918, 40, 822. [all data]

Notes

Go To: Top, Normal boiling point, References

• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.