Pentane
Encyclopedia : P : PE : PEN : Pentane
| Pentane | |
|---|---|
| | |
| General | |
| Systematic name | n-Pentane |
| Other names | Amyl hydride Skellysolve |
| Molecular formula | C5H12 |
| SMILES | CCCCC |
| Molar mass | 72.15 g/mol |
| Appearance | Colourless liquid |
| CAS number | [109-66-0] |
| Properties | |
| Density and phase | 0.626 g/cm3, liquid |
| Solubility in water | 0.01 g/100 ml (20 °C) |
| in hydrocarbons | Fully miscible |
| Melting point | −129.8 °C (143 K) |
| Boiling point | 36.1 °C (308 K) |
| Acidity (pKa) | ~45 |
| Viscosity | 0.240 cP at 20 °C |
| Structure | |
| Molecular shape | |
| Dipole moment | ? D |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | Highly flammable (F+) |
| NFPA 704 | |
| Flash point | −49 °C |
| R/S statement | R: R12, R51/53, R65, R66, R67 S: S2, S9, S16, S29, S33, S61, S62 |
| RTECS number | RZ9450000 |
| Supplementary data page | |
| Structure and properties | n, εr, etc. |
| Thermodynamic data | Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Related compounds | |
| Related alkanes | Butane, Isopentane, Neopentane, Hexane |
| Related compounds | Cyclopentane |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) [Chemical infoboxInfobox disclaimer and references] | |
Chemistry
The conformation (shape) of n-pentane is linear, like that for n-butane; pentane is a longer hydrocarbon than butane.
Three isomers exist for pentane: n-pentane (linear molecule), isopentane (methylbutane) and neopentane (dimethylpropane). The equivalent 5-member ring is cyclopentane.
Uses
Being an unfunctionalized hydrocarbon, pentane is a commodity chemical. It is mainly a fuel and a solvent, although it also could be used as a source of H2 via steam reforming.As the most volatile hydrocarbon that is liquid at room temperature, pentane is often used in the laboratory as a solvent that can be conveniently evaporated. Also because of its nonpolarity and lack of functionality, its dissolving power is poor, thus only non-polar or alkyl-rich compounds are soluble in it. Pentane is completely miscible, however, with many common solvents such as chlorocarbons, aromatics, ethers, but not short chain amines or short chain alcohols.
Reactions
Pentane burns to form carbon dioxide and water:- C5H12 + 8 O2 → 5 CO2 + 6 H2O
As for other hydrocarbons, pentane undergoes free radical chlorination:
- C5H12 + Cl2 → C5H11Cl + HCl
Whereas n-butane is the conventional feedstock in duPont's synthesis maleic anhydride, pentane is also a substrate:
- :CH3CH2CH2CH2CH3 + 5 O2 → C2H2(CO)2O + 5 H2O + CO2
External links
- [Molview from bluerhinos.co.uk] See pentane in 3D
- [Material Safety Data Sheet for Pentane]
- [Phytochemical database entry]
- For a full list of external links to MSDSs, spectroscopic data, commercial chemicals suppliers etc. for this compound, see [Chemical sources].
| Alkanes | |||||||||||||||||||||||||||||||
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Methane CH4 |
| |
Ethane C2H6 |
| |
Propane C3H8 |
| |
Butane C4H10 |
| |
Pentane C5H12 |
| |
Hexane C6H14 | |||||||||||||||||||||
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Heptane C7H16 |
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Octane C8H18 |
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Nonane C9H20 |
| |
Decane C10H22 |
| |
Undecane C11H24 |
| |
Dodecane C12H26 | |||||||||||||||||||||
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