109-66-0

n-Pentane is a flammable liquid. It has applications in industry as an aerosol propellant and as an important component of engine fuel. N-propane is a CNS depressant. Studies with dogs have indicated that it induces cardiac sensitization. In high concentrations it causes incoordination and inhibition of the righting refl exes.

A clear colorless liquid with a petroleum-like odor. Flash point 57°F. Boiling point 97°F. Less dense than water and insoluble in water. Hence floats on water. Vapors are heavier than air.

N-PENTANE(109-66-0) is incompatible with strong oxidizers. N-PENTANE(109-66-0) is also incompatible with strong acids, alkalis, and oxygen. Mixtures with chlorine gas have produced explosions. N-PENTANE(109-66-0) will attack some forms of plastics, rubber, and coatings. .

Highly flammable. Insoluble in water.

Low toxicity. Very high vapor concentrations produce narcosis. Aspiration into lungs can produce chemical pneumonitis and/or pulmonary edema.

Pentane is used in manufacture of ice, low-temperature thermometers; in solvent extraction processes; as a blowing agent in plastics; as a fuel; as a chemical intermediate (for amylchlorides, e.g.).

Behavior in Fire: Containers may explode

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.

UN1265 Pentanes Hazard Class: 3; Labels: 3-Flammable liquid.

Vapors may form explosive mixture with air. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Attacks some plastics, rubbers, and coatings.

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

Clear, colorless, volatile liquid with an odor resembling gasoline. An odor threshold concentration of 1.4 ppm_v was reported by Nagata and Takeuchi (1990).

Fuel; solvent; chemical synthesis

n-Pentane is a flammable liquid. It has diverse uses in industry—for instance, as an aerosol propellant and as an important component of engine fuel. n-Pentane is a CNS depressant. Laboratory studies in dogs indicate that prolonged exposure to high concentrations of n-pentane induces cardiac sensitization, poor coordination, and inhibition of the righting reflexes. NIOSH has recommended limits of n-pentane for working areas.

n-Pentane occurs in volatile petroleum fractions(gasoline) and as a constituent ofpetroleum ether. It is used as a solvent, in themanufacture of low-temperature thermometers,and as a blowing agent for plastics.

A straightchain alkane obtained by distillation of crude oil.

pentane: A straight-chain alkanehydrocarbon, C5H12; r.d. 0.63; m.p.–129.7°C; b.p. 36.1°C. It is obtainedby distillation of petroleum.

Pentane is produced by fractional distillation of natural gas liquids and crude oil. It is also produced by the catalytic crackdown of naphtha.

Extremelyflammable

Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Schauer et al. (1999) reported pentane in a diesel-powered medium-duty truck exhaust at an emission rate of 1,860 μg/km.
A constituent in gasoline. Harley et al. (2000) analyzed the headspace vapors of three grades of unleaded gasoline where ethanol was added to replace methyl tert-butyl ether. The gasoline vapor concentrations of pentane in the headspace were 14.2 wt % for regular grade, 12.6 wt % for midgrade, and 9.3 wt % for premium grade.
California Phase II reformulated gasoline contained pentane at a concentration of 27.6 g/kg. Gas-phase tailpipe emission rates from gasoline-powered automobiles with and without catalytic converters were 4.29 and 536 mg/km, respectively (Schauer et al., 2002).
Schauer et al. (2001) measured organic compound emission rates for volatile organic compounds, gas-phase semi-volatile organic compounds, and particle-phase organic compounds from the residential (fireplace) combustion of pine, oak, and eucalyptus. The gas-phase emission rate of pentane was 4.7 mg/kg of pine burned. Emission rates of pentane were not measured during the combustion of oak and eucalyptus.

Biological. n-Pentane may biodegrade in two ways. The first is the formation of pentyl hydroperoxide, which decomposes to 1-pentanol followed by oxidation to pentanoic acid. The other pathway involves dehydrogenation to 1-pentene, which may react with water giving 1- pentanol (Dugan, 1972). Microorganisms can oxidize alkanes under aerobic conditions (Singer and Finnerty, 1984). The most common degradative pathway involves the oxidation of the terminal methyl group forming 1-pentanol. The alcohol may undergo a series of dehydrogenation steps forming an aldehyde (valeraldehyde) then a fatty acid (valeric acid). The fatty acid may then be metabolized by β-oxidation to form the mineralization products, carbon dioxide and water (Singer and Finnerty, 1984). Mycobacterium smegnatis was capable of degrading pentane to 2- pentanone (Riser-Roberts, 1992).
Photolytic. When synthetic air containing gaseous nitrous acid and pentane was exposed to artificial sunlight (λ = 300–450 nm) methyl nitrate, pentyl nitrate, peroxyacetal nitrate, and peroxypropionyl nitrate formed as products (Cox et al., 1980).
Chemical/Physical. Complete combustion in air yields carbon dioxide and water. Pentane will not hydrolyze because it does not contain a hydrolyzable functional group.

Stir the pentane with successive portions of conc H2SO4 until there is no further coloration during 12hours, then with 0.5N KMnO4 in 3M H2SO4 for 12hours, wash with water and aqueous NaHCO3. Dry it with MgSO4 or Na2SO4, then P2O5 and fractionally distil it through a column packed with glass helices. It is also purified by passage through a column of silica gel, followed by distillation and storage with sodium hydride. An alternative purification is by azeotropic distillation with MeOH, which is subsequently washed out from the distillate (using water), followed by drying and re-distilling. For removal of carbonyl-containing impurities, see n-heptane. Also purify it by fractional freezing (ca 40%) on a copper coil through which cold air is passed, then wash with conc H2SO4 and fractionally distil it. [Beilstein 1 IV 303.]

The mechanism of toxicity is suspected to be similar to other solvents that rapidly induce anesthesia-like effects, that is a ‘nonspecific narcosis’ due to disruption (solvation) of the integrity of the cellular membranes of the central nervous system. The effect is similar to the ‘high’ experienced upon exposure to other aliphatic hydrocarbon solvents.
As seen with other short-chain alkanes, upon inhalation, pentane is moderately toxic and may cause irritation of the respiratory tract and narcosis. The narcotic action of pentane (observed following 1-h exposure to 90 000–120 000 ppm) is, however, much less pronounced than effects seen following exposure to the C1–C4 alkanes. Although the actual biochemical mechanismof toxicity has not been discerned, the narcotic effects seen are most likely related to its physical solvent properties.

The initial threshold screening level (ITSL) for pentane is 17700 μg/m3 based on an 8-hour averaging time.