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Skeletal formula of 2-methylhexane
Skeletal formula of 2-methylhexane with all implicit carbons shown, and all explicit hydrogens added
Ball and stick model of 2-methylhexane
IUPAC name
3D model (Jmol)
ECHA InfoCard 100.008.847
EC Number 209-730-6
RTECS number MO3871500
UN number 3295
Molar mass 100.21 g·mol−1
Appearance Colorless liquid
Odor Odorless
Density 0.679 g cm−3
Melting point −119.0 to −117.8 °C; −182.3 to −180.1 °F; 154.1 to 155.3 K
Boiling point 89.6 to 90.6 °C; 193.2 to 195.0 °F; 362.7 to 363.7 K
Vapor pressure 15.7 kPa (at 37.7 °C)
19 nmol Pa−1 kg−1
-86.24·10−6 cm3/mol
222.92 J K−1 mol−1
323.34 J K−1 mol−1
−231.1–−228.5 kJ mol−1
−4.8127–−4.8103 MJ mol−1
GHS pictograms The flame pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The health hazard pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) The environment pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal word DANGER
H225, H304, H315, H336, H410
P210, P261, P273, P301+310, P331
Highly Flammable F Harmful Xn Dangerous for the Environment (Nature) N
R-phrases R11, R38, R50/53, R65, R67
S-phrases (S2), S16, S29, S33
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasoline) Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point −1 °C (30 °F; 272 K)
280 °C (536 °F; 553 K)
Explosive limits 1–7%
Related compounds
Related alkanes
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

2-Methylhexane (C7H16, also known as isoheptane, ethylisobutylmethane) is an isomer of heptane. It is structurally a hexane molecule with a methyl group attached to its second carbon atom. It exists in most commercially available heptane merchandises as an impurity but is usually not considered as impurity in terms of reactions since it has very similar physical and chemical properties when compared to n-heptane (straight-chained heptane).

Being an alkane, 2-methylhexane is insoluble in water, but is soluble in many organic solvents, such as alcohols and ether. However, 2-methylhexane is more commonly considered as a solvent itself. Therefore, even though it is present in many commercially available heptane products, it is not considered as a destructive impurity, as heptane is usually used as a solvent. Nevertheless, by concise processes of distillation and refining, it is possible to separate 2-methylhexane from n-heptane.

Within a group of isomers, those with more branches tend to ignite more easily and combust more completely. Therefore, 2-methylhexane has a lower Autoignition temperature and flash point when compared to heptane. Theoretically 2-methylhexane also burns with a less sooty flame, emitting higher-frequency radiation; however, as heptane and 2-methylhexane differ by only one carbon atom, in terms of branching, both burn with a bright yellow flame when ignited.

Compared to n-heptane, 2-methylhexane also has lower melting and boiling points. A lower density of liquid is found in 2-Methylhexane than heptane.

On the NFPA 704 scale, 2-methylhexane is listed as a reactivity level-0 chemical, along with various other alkanes. In fact, most alkanes are unreactive except in extreme conditions, such as combustion or strong sunlight. At the presence of oxygen and flame, 2-methylhexane, like heptane, combusts mostly completely into water and carbon dioxide. With UV-light and mixed with halogens in solvents, usually bromine in 1,1,1-trichloroethane, a substitution reaction occurs.

See also[edit]


  1. ^ "2-METHYLHEXANE - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification and Related Records. Retrieved 6 March 2012. 
  • "2-Methylhexane". chemexper.com. Retrieved 22 November 2011. 
  • "Material Safety Data Sheet" (PDF). ChemADVISOR. Retrieved 22 November 2011. 
  • "Isoheptane". INCHEM: Chemical Safety Information from Intergovernmental Organizations. International Programme on Chemical Safety. October 2002. Retrieved 22 November 2011.