Hexane

Hexane
Names
Preferred IUPAC name
Hexane[1]
Other names
Sextane,[2] hexacarbane
Identifiers
CAS Number
3D model (JSmol)
Beilstein Reference
 1730733
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.435
Edit this at Wikidata
EC Number
  • 203-777-6
Gmelin Reference
 1985
KEGG
MeSH n-hexane
PubChem CID
RTECS number
  • MN9275000
UNII
UN number 1208
InChI
  • InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3 checkY
    Key: VLKZOEOYAKHREP-UHFFFAOYSA-N checkY
SMILES
  • CCCCCC
Properties
Chemical formula
 C6H14
Molar mass 86.178 g·mol−1
Appearance Colorless liquid
Odor Petrolic
Density 0.6606 g mL−1[3]
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)
Henry's law
constant (kH)
 7.6 nmol Pa−1 kg−1
UV-vis (λmax) 200 nm
Magnetic susceptibility (χ)
 −74.6·10−6 cm3/mol
Refractive index (nD)
 1.375
Viscosity 0.3 mPa·s
Dipole moment
 0.08 D
Thermochemistry
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 (ΔfH⦵298)
 −199.4–−198.0 kJ mol−1
Std enthalpy of
combustion (ΔcH⦵298)
 −4180–−4140 kJ mol−1
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Reproductive toxicity – After aspiration, pulmonary oedema, pneumonitis[4]
GHS labelling:
Pictograms
Signal word
 Danger
Hazard statements
 H225, H302, H305, H315, H336, H361fd, H373, H411
Precautionary statements
 P201, P202, P210, P233, P235, P240, P241, P242, P243, P260, P264, P271, P273, P280, P281, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P308+P313, P310, P312, P314, P332+P313, P363, P370+P378, P391, P403+P233, P405, P501
NFPA 704 (fire diamond)
1
3
0
Flash point −26.0 °C (−14.8 °F; 247.2 K)
Autoignition
temperature
 234.0 °C (453.2 °F; 507.1 K)
Explosive limits 1.2–7.7%
Lethal dose or concentration (LD, LC):
25 g kg−1 (oral, rat)
28710 mg/kg (rat, oral)[5]
56137 mg/kg (rat, oral)[5]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 500 ppm (1800 mg/m3)[6]
REL (Recommended)
 TWA 50 ppm (180 mg/m3)[6]
IDLH (Immediate danger)
 1100 ppm[6]
Related compounds
Related alkanes
Supplementary data page
Hexane (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Hexane (/ˈhɛkseɪn/) is an organic compound, a straight-chain alkane with six carbon atoms and has the molecular formula C6H14.

Hexane is a significant constituent of gasoline. It is a colorless liquid, odorless when pure, and with boiling points approximately 69 °C (156 °F). It is widely used as a cheap, relatively safe, largely unreactive, and easily evaporated non-polar solvent.

The term hexanes refers to a mixture, composed largely (>60%) of hexane, with varying amounts of the isomeric compounds 2-methylpentane and 3-methylpentane, and, possibly, smaller amounts of nonisomeric C5, C6, and C7 (cyclo)alkanes. Hexanes are cheaper than hexane and are often used in large-scale operations not requiring a single isomer (e.g., as cleaning solvent or for chromatography).

Isomers

Common name IUPAC name Text formula Skeletal formula
normal hexane
n-hexane		 hexane CH3(CH2)4CH3
isohexane 2-methylpentane (CH3)2CH(CH2)2CH3
3-methylpentane CH3CH2CH(CH3)CH2CH3
2,3-dimethylbutane (CH3)2CHCH(CH3)2
neohexane 2,2-dimethylbutane (CH3)3CCH2CH3

Uses

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 or soy oil) from seeds, for cleansing and degreasing a variety of items, and in textile manufacturing. They are commonly used in food based soybean oil extraction in the United States, and are potentially present as contaminants in all soy food products in which the technique is used; the lack of regulation by the FDA of this contaminant is a matter of some controversy.[7][8]

A typical laboratory use of hexanes is to extract oil and grease contaminants from water and soil for analysis.[9] 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.[10]

Hexanes are commonly used in chromatography as a non-polar solvent. Higher alkanes present as impurities in hexanes have similar retention times as the solvent, meaning that fractions containing hexane will also contain these impurities. In preparative chromatography, concentration of a large volume of hexanes can result in a sample that is appreciably contaminated by alkanes. This may result in a solid compound being obtained as an oil and the alkanes may interfere with analysis.[11]

Production

Hexanes are chiefly obtained by refining 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 (149–158 °F).

Physical properties

All alkanes are colorless.[12][13] 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.[14]

Isomer M.P. (°C) M.P. (°F) B.P. (°C) B.P. (°F)
n-hexane−95.3 −139.568.7 155.7
3-methylpentane−118.0 −180.463.3 145.9
2-methylpentane (isohexane)−153.7 −244.760.3 140.5
2,3-dimethylbutane−128.6 −199.558.0 136.4
2,2-dimethylbutane (neohexane)−99.8 −147.649.7 121.5

Hexane has considerable vapor pressure at room temperature:

Temperature (°C) Temperature (°F) Vapor pressure (mmHg) Vapor pressure (kPa)
−40 −403.36 0.448
−30 −227.12 0.949
−20 −414.01 1.868
−10 1425.91 3.454
0 3245.37 6.049
10 5075.74 10.098
20 68121.26 16.167
25 77151.28 20.169
30 86187.11 24.946
40 104279.42 37.253
50 122405.31 54.037
60 140572.76 76.362

Reactivity

Like most alkanes, hexane characteristically exhibits low reactivity and are suitable solvents for reactive compounds. Commercial samples of n-hexane however often contains methylcyclopentane, which features tertiary C-H bonds, which are incompatible with some radical reactions.[15]

Safety

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, and paresthesia in the distal extremities; 2500–5000 ppm produces muscle weakness, cold pulsation in the extremities, blurred vision, headache and anorexia.[16] Chronic occupational exposure to elevated levels of n-hexane has been demonstrated to be associated with peripheral neuropathy in auto mechanics in the US, and neurotoxicity in workers in printing presses, and shoe and furniture factories in Asia, Europe, and North America.[17]

The US National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) for hexane isomers (not n-hexane) of 100 ppm (350 mg/m3 (0.15 gr/cu ft)) over an 8-hour workday.[18] However, for n-hexane, the current NIOSH REL is 50 ppm (180 mg/m3 (0.079 gr/cu ft)) over an 8-hour workday.[19] This limit was proposed as a permissible exposure limit (PEL) by the Occupational Safety and Health Administration in 1989; however, this PEL was overruled in US courts in 1992.[20] The current n-hexane PEL in the US is 500 ppm (1,800 mg/m3 (0.79 gr/cu ft)).[19]

Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk.[21] n-Hexane 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 solvents.[22]

Like gasoline, hexane is highly volatile and is an explosion risk. Ignition of hexane vapors which had been illegally discharged in the sewers of Louisville (Kentucky) from a soybean processing plant owned by Ralston-Purina caused a series of explosions which destroyed more over 21 km of sewer lines and streets in that city.

Incidents

Occupational hexane poisoning has occurred with Japanese sandal workers, Italian shoe workers,[23] Taiwan press proofing workers, and others.[24] Analysis of Taiwanese workers has shown occupational exposure to substances including n-hexane.[25] In 2010–2011, Chinese workers manufacturing iPhones were reported to have suffered hexane poisoning.[26][27]

Hexane was identified as being the cause of the Louisville sewer explosions on 13 February 1981, that destroyed more than 13 miles (21 km) of sewer lines and streets in the center of Louisville in Kentucky, United States

Biotransformation

n-Hexane is biotransformed to 2-hexanol and further to 2,5-hexanediol in the body. The conversion is catalyzed by the enzyme cytochrome P450 utilizing oxygen from air. 2,5-Hexanediol may be further oxidized to 2,5-hexanedione, which is neurotoxic and produces a polyneuropathy.[22] In view of this behavior, replacement of n-hexane as a solvent has been discussed. n-Heptane is a possible alternative.[28]

See also

  • Cyclohexane

References

  1. ↑ "n-hexane – Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification and Related Records. Archived from the original on 8 March 2012. Retrieved 31 December 2011.
  2. ↑ Hofmann, August Wilhelm Von (1 January 1867). "I. On the action of trichloride of phosphorus on the salts of the aromatic monamines". Proceedings of the Royal Society of London. 15: 54–62. doi:10.1098/rspl.1866.0018. S2CID 98496840.
  3. ↑ William M. Haynes (2016). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton: CRC Press. pp. 3–298. ISBN 978-1-4987-5429-3.
  4. ↑ GHS Classification on [PubChem]
  5. 1 2 "n-Hexane". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  6. 1 2 3 NIOSH Pocket Guide to Chemical Hazards. "#0322". National Institute for Occupational Safety and Health (NIOSH).
  7. ↑ "The Tofurky Company : Our Ingredients". Tofurky.com. Archived from the original on 17 March 2015. Retrieved 17 March 2015.
  8. ↑ Palmer, Brian (26 April 2010). "A study found hexane in soy protein. Should you stop eating veggie burgers?". Slate.com. Archived from the original on 9 March 2015. Retrieved 17 March 2015.
  9. ↑ Use of ozone depleting substances in laboratories. Kbh: Nordisk Ministerråd. 2003. ISBN 92-893-0884-2. OCLC 474188215. Archived from the original on 16 July 2012.
  10. ↑ Schwindeman, James A.; Woltermann, Chris J.; Letchford, Robert J. (1 May 2002). "Safe handling of organolithium compounds in the laboratory". Chemical Health & Safety. 9 (3): 6–11. doi:10.1016/s1074-9098(02)00295-2. ISSN 1074-9098.
  11. ↑ "The Hexane Molecule". www.worldofmolecules.com. Retrieved 30 December 2021.
  12. ↑ "Organic Chemistry-I" (PDF). Nsdl.niscair.res.in. Archived from the original (PDF) on 29 October 2013. Retrieved 17 February 2014.
  13. ↑ "13. Hydrocarbons | Textbooks". Textbook.s-anand.net. Archived from the original on 6 October 2014. Retrieved 17 February 2014.
  14. ↑ William D. McCain (1990). The properties of petroleum fluids. PennWell. ISBN 978-0-87814-335-1.
  15. ↑ Koch, H.; Haaf, W. (1973). "1-Adamantanecarboxylic Acid". Organic Syntheses.; Collective Volume, vol. 5, p. 20
  16. ↑ "N-HEXANE". Toxicology data network Hazardous Substances Data Bank. National Library of Medicine. Archived from the original on 4 September 2015.
  17. ↑ Centers for Disease Control and Prevention (CDC) (16 November 2001). "n-Hexane-related peripheral neuropathy among automotive technicians--California, 1999-2000". MMWR. Morbidity and Mortality Weekly Report. 50 (45): 1011–1013. ISSN 0149-2195. PMID 11724159.
  18. ↑ "CDC – NIOSH Pocket Guide to Chemical Hazards – Hexane isomers (excluding n-Hexane)". cdc.gov. Archived from the original on 31 October 2015. Retrieved 3 November 2015.
  19. 1 2 CDC (28 March 2018). "n-Hexane". Centers for Disease Control and Prevention. Retrieved 3 May 2020.
  20. ↑ "Appendix G: 1989 Air Contaminants Update Project - Exposure Limits NOT in Effect". www.cdc.gov. 20 February 2020. Retrieved 3 May 2020.
  21. ↑ Gad, Shayne C (2005), "Petroleum Hydrocarbons", Encyclopedia of Toxicology, vol. 3 (2nd ed.), Elsevier, pp. 377–379
  22. 1 2 Clough, Stephen R; Mulholland, Leyna (2005). "Hexane". Encyclopedia of Toxicology. Vol. 2 (2nd ed.). Elsevier. pp. 522–525.
  23. ↑ 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. doi:10.1159/000115166. PMID 6249607.
  24. ↑ n-Hexane, Environmental Health Criteria, World Health Organization, 1991, archived from the original on 19 March 2014
  25. ↑ Liu, C. H.; Huang, C. Y.; Huang, C. C. (2012). "Occupational Neurotoxic Diseases in Taiwan". Safety and Health at Work. 3 (4): 257–67. doi:10.5491/SHAW.2012.3.4.257. PMC 3521924. PMID 23251841.
  26. ↑ "Workers poisoned while making iPhones – ABC News (Australian Broadcasting Corporation)". Australian Broadcasting Corporation. 26 October 2010. Archived from the original on 8 April 2011. Retrieved 17 March 2015.
  27. ↑ David Barboza (22 February 2011). "Workers Sickened at Apple Supplier in China". The New York Times. Archived from the original on 7 April 2015. Retrieved 17 March 2015.
  28. ↑ 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. Advances in Experimental Medicine and Biology. 387: 411–427. doi:10.1007/978-1-4757-9480-9_50. ISBN 978-1-4757-9482-3. PMID 8794236.
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