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Pentane

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Pentane
n-Pentane 3D structure of a pentane molecule
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]
Pentane, also known as amyl hydride or skellysolve A is an alkane hydrocarbon. It is a liquid commodity chemical compound, mainly used as fuel and as a solvent.

Chemistry

The conformation (shape) of n-pentane is linear, like that for n-butane; pentane is a longer hydrocarbon than butane.

Isomers of Pentane
Isomers of Pentane

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
When oxygen is limited, carbon, partially oxidized carbon (soot), and carbon monoxide are also formed.

As for other hydrocarbons, pentane undergoes free radical chlorination:

C5H12 + Cl2 → C5H11Cl + HCl
Such reactions are unselective, yielding a mixture of the 1-, 2-, and 3-chloropentanes, as well as more highly chlorinated derivatives. Other radical halogenations can also occur.

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


 
Alkanes
Methane
CH4
|
 
Ethane
C2H6
|
 
Propane
C3H8
|
 
Butane
C4H10
|
 
Pentane
C5H12
|
 
Hexane
C6H14
Heptane
C7H16
|
 
Octane
C8H18
|
 
Nonane
C9H20
|
 
Decane
C10H22
|
 
Undecane
C11H24
|
 
Dodecane
C12H26
 

 


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