Hexane

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Not to be confused with hexene or hexyne.
Hexane
Skeletal formula of hexane
Skeletal formula of hexane with all implicit carbons shown, and all explicit hydrogens added
Ball and stick model of hexane
Spacefill model of hexane
Identifiers
CAS number 110-54-3 YesY
PubChem 8058
ChemSpider 7767 YesY
UNII 2DDG612ED8 YesY
EC number 203-777-6
UN number 1208
DrugBank DB02764
KEGG C11271 YesY
MeSH n-hexane
ChEBI CHEBI:29021 YesY
ChEMBL CHEMBL15939 YesY
RTECS number MN9275000
Beilstein Reference 1730733
Gmelin Reference 1985
Jmol-3D images Image 1
Properties
Molecular formula C6H14
Molar mass 86.18 g mol−1
Appearance Colorless liquid
Odor Petrolic
Density 0.6548 g mL−1
Melting point −96 to −94 °C; −141 to −137 °F; 177 to 179 K
Boiling point 68.5 to 69.1 °C; 155.2 to 156.3 °F; 341.6 to 342.2 K
Solubility in water 9.5 mg L−1
log P 3.764
Vapor pressure 17.60 kPa (at 20.0 °C)
kH 7.6 nmol Pa−1 kg−1
λmax 200 nm
Refractive index (nD) 1.375
Viscosity 294 μPa s
Thermochemistry
Specific
heat capacity
C
265.2 J K−1 mol−1
Std molar
entropy
So298
296.06 J K−1 mol−1
Std enthalpy of
formation
ΔfHo298
−199.4–−198.0 kJ mol−1
Std enthalpy of
combustion
ΔcHo298
−4180–−4140 kJ mol−1
Hazards
MSDS External MSDS
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
GHS hazard statements H225, H304, H315, H336, H373, H411
GHS precautionary statements P210, P261, P273, P281, P301+310, P331
EU Index 601-037-00-0
EU classification Highly Flammable F Harmful Xn Dangerous for the Environment (Nature) N
R-phrases R11, R38, R48/20, R51/53, R62, R65, R67
S-phrases (S2), S16, S29, S33, S36/37
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 −26.0 °C (−14.8 °F; 247.2 K)
Explosive limits 1.2–7.7%
U.S. Permissible
exposure limit (PEL)
500 ppm (1800 mg m-3 as an 8 h TWA)
LD50 25 g kg−1 (oral, rat)
Related compounds
Related alkanes
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Hexane /ˈhɛksn/ is an alkane of six carbon atoms, with the chemical formula C6H14.

The term may refer to any of the five structural isomers with that formula, or to a mixture of them.[2] In IUPAC nomenclature, however, hexane is the unbranched isomer (n-hexane); the other four structures are named as methylated derivatives of pentane and butane. IUPAC also uses the term as the root of many compounds with a linear six-carbon backbone, such as 2-methylhexane (C7H16), which is also called "isoheptane".

Hexanes are significant constituents of gasoline. They are all colorless liquids at room temperature, odorless when pure, with boiling points between 50 and 70 °C. They are widely used as cheap, relatively safe, largely unreactive, and easily evaporated non-polar solvents.

Isomers[edit]

Common name IUPAC name Text formula Skeletal formula
normal hexane
n-hexane
hexane CH3(CH2)4CH3 Hexane-2D-Skeletal.svg
isohexane 2-methylpentane (CH3)2CH(CH2)2CH3 2-metilpentāns.svg
3-methylpentane CH3CH2CH(CH3)CH2CH3 3-metilpentāns.svg
2,3-dimethylbutane CH3CH(CH3)CH(CH3)CH3 2,3-dimetilbutāns.svg
neohexane 2,2-dimethylbutane CH3C(CH3)2CH2CH3 2,2-dimetilbutāns.svg

Uses[edit]

In industry, hexanes are used in the formulation of glues for shoes, leather products, and roofing. They are also used to extract cooking oils (such as canola oil) from seeds, for cleansing and degreasing a variety of items, and in textile manufacturing.

A typical laboratory use of hexanes is to extract oil and grease contaminants from water and soil for analysis.[3] Since hexane cannot be easily deprotonated, it is used in the laboratory for reactions that involve very strong bases, such as the preparation of organolithiums. For example, butyllithiums are typically supplied as a hexane solution.

In many applications (especially pharmaceutical), the use of n-hexane is being phased out due to its long term toxicity. It is often replaced by n-heptane, which will not form the toxic metabolite hexane-2,5-dione.[4]

Production[edit]

Hexanes are chiefly obtained by the refining of crude oil. The exact composition of the fraction depends largely on the source of the oil (crude or reformed) and the constraints of the refining. The industrial product (usually around 50% by weight of the straight-chain isomer) is the fraction boiling at 65–70 °C.

Physical properties[edit]

All alkanes are colorless.[5][6] The boiling points of the various hexanes are somewhat similar and, as for other alkanes, are generally lower for the more branched forms. The melting points are quite different and the trend is not apparent.[7]

Isomer M.P. (°C) B.P. (°C)
n-hexane −95.3 68.7
3-methylpentane −118.0 63.3
2-methylpentane (isohexane) −153.7 60.3
2,3-dimethylbutane −128.6 58.0
2,2-dimethylbutane (neohexane) −99.8 49.7

Hexane has considerable vapor pressure at room temperature:[8]

Temperature (°C) Vapor pressure (mmHg)
−40 3.36
−30 7.12
−20 14.01
−10 25.91
0 45.37
10 75.74
20 121.26
25 151.28
30 187.11
40 279.42
50 405.31
60 572.76

Safety[edit]

Acute exposure to n-hexane usually occurs by inhalation, but it may be absorbed orally and transdermally. Minor exposures may occur when persons fill their automobile fuel tanks with gasoline. Recent research suggests that certain fungi may be able to produce n-hexane.[9]

The acute toxicity of n-hexane is rather low. However, it has been reported to be the most highly toxic member of the alkanes.[citation needed] When n-hexane is ingested, it causes nausea, vertigo, bronchial irritation, intestinal irritation and CNS effects. It has been reported that ~50 g of n-hexane may be fatal to humans. Furthermore, n-hexane is biotransformed to 2-hexanol and further to 2,5-hexanediol by cytochrome P450 mixed function oxidases by omega oxidation. 2,5-Hexanediol may be further oxidized to 2,5-hexanedione, which is neurotoxic and produces a polyneuropathy.[9]

n-Hexane is also used as a solvent in the extraction of oil from seeds (soybean, cottonseed, flaxseed, safflower seed, and others). It is sometimes used as a denaturant for alcohol, and as a cleaning agent in the textile, furniture, and leather industries. It is slowly being replaced with other less toxic solvents.[9]

The National Institute for Occupational Safety and Health recommended exposure limit is 50 ppm (180 mg m−3), expressed as an 8 h time-weighted average (TWA).[9] A peer reviewed study found that inhalation of n-hexane at 5000 ppm for 10 minutes produces marked vertigo; 2500-1000 ppm for 12 hours produces drowsiness, fatigue, loss of appetite, paresthesia in distal extremities; 2500-500 ppm produces muscle weakness, cold pulsation in extremities, blurred vision, headache and anorexia.[10]

Occupational hexane poisoning has occurred with Japanese sandal workers, Italian shoe workers,[11] Taiwan press proofing workers, and others.[12] Analysis of Taiwanese workers has shown occupational exposure to substances including n-hexane.[13] In 2010-2011, Chinese workers manufacturing iPhones were reported as having suffered hexane poisoning.[14][15]

References[edit]

  1. ^ "n-hexane – Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification and Related Records. Retrieved 31 December 2011. 
  2. ^ "C5 and C6 alkanes". A and B Scott Organic Chemistry. Retrieved 30 October 2007. 
  3. ^ Use of ozone depleting substances in laboratories. TemaNord 2003:516.
  4. ^ Filser JG, Csanády GA, Dietz W, Kessler W, Kreuzer PE, Richter M, Störmer A (1996). "Comparative estimation of the neurotoxic risks of n-hexane and n-heptane in rats and humans based on the formation of the metabolites 2,5-hexanedione and 2,5-heptanedione". Adv Exp Med Biol 387: 411–427. PMID 8794236. 
  5. ^ "Organic Chemistry-I" (PDF). Retrieved 2014-02-17. 
  6. ^ "13. Hydrocarbons | Textbooks". Textbook.s-anand.net. Retrieved 2014-02-17. 
  7. ^ William D. McCain (1990). The properties of petroleum fluids. PennWell. ISBN 0-87814-335-1. 
  8. ^ vapor pressure
  9. ^ a b c d Stephen R Clough; Leyna Mulholland (2005), "Hexane", Encyclopedia of Toxicology 2 (2nd ed.), Elsevier, pp. 522–525 
  10. ^ "N-HEXANE". Toxicology data network Hazardous Substances Data Bank. National Library of Medicine. 
  11. ^ Rizzuto, N; De Grandis, D; Di Trapani, G; Pasinato, E (1980). "N-hexane polyneuropathy. An occupational disease of shoemakers". European neurology 19 (5): 308–15. PMID 6249607.  edit
  12. ^ n-Hexane, Environmental Health Criteria (122), World Health Organization, 1991 
  13. ^ Liu, C. H.; Huang, C. Y.; Huang, C. C. (2012). "Occupational Neurotoxic Diseases in Taiwan". Safety and Health at Work 3 (4): 257. doi:10.5491/SHAW.2012.3.4.257. PMC 3521924. PMID 23251841.  edit
  14. ^ Workers poisoned while making iPhones ABC News, 25 October 2010
  15. ^ David Barboza (Feb 22, 2011). "Workers Sickened at Apple Supplier in China". New York Times. 

External links[edit]