Pentane
Distilled lab-grade pentane.
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Names | |
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IUPAC name
Pentane
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Systematic IUPAC name
n-Pentane | |
Identifiers | |
Jmol-3D images | Image |
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Properties | |
C5H12 | |
Molar mass | 72.15 g/mol |
Appearance | Colorless volatile liquid |
Odor | Lighter-fluid like |
Density | 0.626 g/cm3 |
Melting point | −129.8 °C (−201.6 °F; 143.3 K) (decomposes) |
Boiling point | 36 °C (97 °F; 309 K) |
40 mg/L (at 20 °C) | |
Vapor pressure | 57.90 kPa (at 20.0 °C) |
Acidity (pKa) | ~45 |
Viscosity | 0.240 cP (at 20 °C) |
Thermochemistry | |
Std molar
entropy (S |
263.47 J K−1 mol−1 |
Std enthalpy of
formation (ΔfH |
−174.1–−172.9 kJ mol−1 |
Hazards | |
Safety data sheet | BOC |
Flash point | −49 °C |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
3 g kg−1 (dermal, rabbit) 5 g kg−1 (oral, mouse) |
LC50 (Median concentration)
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130,000 mg/m3 (mouse, 30 min) 128,200 ppm (mouse, 37 min) 325,000 mg/m3 (mouse, 2 hr) |
Related compounds | |
Related compounds
|
Butane Hexane |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Contents
Properties
Chemical
Pentane, like other hydrocarbons, will burn in air when ignited by an open flame to release carbon dioxide and water vapor.
Physical
Pentane is a colorless liquid hydrocarbon, with a characteristic smell. It is insoluble in water, but miscible with other organic solvents. It has a density of 0.621 g/cm3, meaning it's lighter than water. It boils at 36°C and melts at -130°C.
Its isomer neopentane, though, is a gas that boils at 9.5°C, is the heaviest and the most high-boiling of all hydrocarbon gases.
Availability
Pentane can be purchased form chemical suppliers. Certain pesticides contain pentane.
Some car starter fluids contain pentane to increase the volatility of the fluid. You will need a long fractional distillation column or repeated distillations, as the boiling point of diethyl ether (34.6 °C), the other useful compound from starter fluid, is very close to that of pentane (36.3 °C).
Some type of charcoal lighter fluids can contain up to 25% n-pentane. Fractional distillation is required to extract it from the mixture.
Preparation
Pentane can be prepared by decarboxylating the salts of caproic acid, found in various oily plants, with a strong base.
Projects
- Extraction (solvent)
- Phthalic and maleic anhydride synthesis
Handling
Safety
Pentane evaporates very fast and the vapors are hazardous if inhaled, work should be performed in a fumehood or outside. If pentane is inhaled in large amounts, further exposure should be limited and one should seek fresh air.
Storage
Due to its low boiling point, pentane should be stored in closed glass bottles, at constant temperature, away from any source of heat, even small ones. If it's stored at low temperatures, and then brought at room temperatures or slightly higher, pressure will build up in the bottle from the vapors and the bottle can explode. It is mandatory to open the bottle from time to time, to release the pressure.
Commercial pentane contains small amounts of inhibitors, that prevent its degradation, over long periods of time. They can be removed by distillation, as their boiling point is much higher than that of pentane.
Disposal
Pentane can be safely burned, as it theoretically should not generate any toxic byproducts. However, like other hydrocarbons, carbon monoxide can be formed so this should not be performed indoors.
References
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- Chemical compounds
- Organic compounds
- Hydrocarbons
- Alkanes
- Solvents
- Nonpolar solvents
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