Jump to content

Hexane: Difference between revisions

From Wikipedia, the free encyclopedia
Browse history interactively
← Previous edit
Content deleted Content added
VisualWikitext
Alph Bot (talk | contribs)
16,072 edits
m robot Modifying: hu:Hexán, nl:N-hexaan
 
(435 intermediate revisions by more than 100 users not shown)
Line 1: Line 1:
{{short description|Chemical compound}}
{{chembox
{{Distinguish|hexene|hexyne}}
| Watchedfields = changed
{{Use dmy dates|date=November 2020}}
| verifiedrevid = 306466069
{{Chembox
| Name = ''n''-Hexane
| Watchedfields = changed
| ImageFile = Hexane-2D-Skeletal.svg
| verifiedrevid = 443856572
| ImageFile1 = Hexane-2D-flat-B.png
| Name =
| ImageFile2 = Hexane-from-xtal-1999-at-an-angle-3D-balls.png
| ImageFile3 = Hexane-3D-vdW.png
| ImageFile = Hexane-2D-Skeletal.svg
| ImageFile_Ref = {{chemboximage|correct|??}}
| IUPACName = Hexane
| ImageSize = 160
| OtherNames = ''n''-Hexane
| ImageName = Skeletal formula of hexane
| Section1 = {{Chembox Identifiers
| ImageFile1 = Hexane-2D-B.png
| SMILES = CCCCCC
| ImageFile1_Ref = {{chemboximage|correct|??}}
| InChI = 1/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3
| ImageName1 = Skeletal formula of hexane with all implicit carbons shown, and all explicit hydrogens added
| CASNo_Ref = {{cascite}}
| ImageFile2 = Hexane-from-xtal-1999-at-an-angle-3D-balls.png
| ImageFile2_Ref = {{chemboximage|correct|??}}
| ImageSize2 = 160
| ImageName2 = Ball and stick model of hexane
| ImageFile3 = Hexane-3D-vdW.png
| ImageFile3_Ref = {{chemboximage|correct|??}}
| ImageSize3 = 160
| ImageName3 = Spacefill model of hexane
| PIN = Hexane<ref>{{cite web|title=n-hexane – Compound Summary|url=https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=8058&loc=ec_rcs|work=PubChem Compound|publisher=National Center for Biotechnology Information|access-date=31 December 2011|location=USA|date=16 September 2004|at=Identification and Related Records|url-status=live|archive-url=https://web.archive.org/web/20120308173754/http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=8058|archive-date=8 March 2012}}</ref>
| OtherNames = Sextane,<ref>{{cite journal|title=I. On the action of trichloride of phosphorus on the salts of the aromatic monamines|first=August Wilhelm Von|last=Hofmann|date=1 January 1867|journal=Proceedings of the Royal Society of London|volume=15|pages=54–62|doi=10.1098/rspl.1866.0018|s2cid=98496840}}</ref> hexacarbane
| SystematicName =
| Section1 = {{Chembox Identifiers
| CASNo = 110-54-3
| CASNo = 110-54-3
| CASNo_Ref = {{cascite|correct|CAS}}
| RTECS = MN9275000
| ChemSpiderID = 7767
| PubChem = 8058
| PubChem = 8058
| ChemSpiderID = 7767
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| UNII = 2DDG612ED8
| UNII_Ref = {{fdacite|correct|FDA}}
| EINECS = 203-777-6
| UNNumber = 1208
| DrugBank = DB02764
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| KEGG = C11271
| KEGG_Ref = {{keggcite|correct|kegg}}
| MeSHName = n-hexane
| ChEBI = 29021
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 15939
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| RTECS = MN9275000
| Beilstein = 1730733
| Gmelin = 1985
| SMILES = CCCCCC
| StdInChI = 1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = VLKZOEOYAKHREP-UHFFFAOYSA-N
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
}}
}}
| Section2 = {{Chembox Properties
| Section2 = {{Chembox Properties
| C=6 | H=14
| Formula = C<sub>6</sub>H<sub>14</sub>
| MolarMass = 86.18 g/mol
| Appearance = Colorless liquid
| Appearance = Colorless liquid
| Odor = Petrolic
| Density = 0.6548 g/ml, liquid
| Density = 0.6606 g mL<sup>−1</sup><ref name="crc97">{{cite book | author=William M. Haynes | title=CRC Handbook of Chemistry and Physics | edition=97th | year=2016 | publisher=CRC Press | location=Boca Raton | isbn=978-1-4987-5429-3 | pages=3–298 | url=https://books.google.com/books?id=VVezDAAAQBAJ}}</ref>
| Solubility = 13 mg/l at 20°C<ref>[http://www.inchem.org/documents/icsc/icsc/eics0279.htm n-Hexane], Date of Peer Review: April 2000</ref>
| MeltingPt = −95 °C (178 K)
| MeltingPtK = 177 to 179
| BoilingPt = 69 °C (342 K)
| BoilingPtK = 341.6 to 342.2
| Solubility = 9.5 mg L<sup>−1</sup>
| Viscosity = 0.294 [[Poise|cP]] at 25 °C
| LogP = 3.764
| VaporPressure = 17.60 kPa (at 20.0&nbsp;°C)
| HenryConstant = 7.6 nmol Pa<sup>−1</sup> kg<sup>−1</sup>
| LambdaMax = 200 nm
| RefractIndex = 1.375
| Viscosity = 0.3 mPa·s
| Dipole = 0.08 D
| MagSus = −74.6·10<sup>−6</sup> cm<sup>3</sup>/mol
}}
| Section3 = {{Chembox Thermochemistry
| DeltaHf = −199.4–−198.0 kJ mol<sup>−1</sup>
| DeltaHc = −4180–−4140 kJ mol<sup>−1</sup>
| Entropy = 296.06 J K<sup>−1</sup> mol<sup>−1</sup>
| HeatCapacity = 265.2 J K<sup>−1</sup> mol<sup>−1</sup>
}}
}}
| Section7 = {{Chembox Hazards
| Section4 = {{Chembox Hazards
| MainHazards = [[Reproductive toxicity]] – After [[Pulmonary aspiration|aspiration]], [[pulmonary oedema]], [[pneumonitis]]<ref name=":1">GHS Classification on [https://pubchem.ncbi.nlm.nih.gov/compound/8058#section=Safety-and-Hazards <nowiki>[PubChem]</nowiki>]</ref>
| EUClass = Flammable ('''F''')<br />Harmful ('''Xn''')<br />Repr. Cat. 3<br />Dangerous for<br />the environment ('''N''')
| GHSPictograms = {{GHS flame}} {{GHS exclamation mark}} {{GHS health hazard}} {{GHS environment}}
| GHSSignalWord = '''DANGER'''
| HPhrases = {{H-phrases|225|302|305|315|336|361fd|373|411}}
| PPhrases = {{P-phrases|201|202|210|233|240|241|242|243|260|264|271|273|280|281|301+330+331|310|302+352|303+361+353|304+340|312|308+313|314|332+313|363|370+378|391|403+233|235|405|501}}
| NFPA-H = 1
| NFPA-H = 1
| NFPA-F = 3
| NFPA-F = 3
| NFPA-R =
| NFPA-R = 0
| FlashPtC = −26.0
| RPhrases = {{R11}}, {{R38}}, {{R48/20}}, {{R62}},<br />{{R65}}, {{R67}}, {{R51/53}}
| AutoignitionPtC = 234.0
| SPhrases = {{S2}}, {{S9}}, {{S16}}, {{S29}}, {{S33}},<br />{{S36/37}}, {{S61}}, {{S62}}
| ExploLimits = 1.2–7.7%
| FlashPt = −23.3 °C
| LD50 = 25 g kg<sup>−1</sup> <small>(oral, rat)</small><br/>28710 mg/kg (rat, oral)<ref name=IDLH>{{IDLH|110543|n-Hexane}}</ref>
| Autoignition = 233.9 °C
| LDLo = 56137 mg/kg (rat, oral)<ref name=IDLH/>
| PEL = TWA 500 ppm (1800 mg/m<sup>3</sup>)<ref name=PGCH>{{PGCH|0322}}</ref>
| REL = TWA 50 ppm (180 mg/m<sup>3</sup>)<ref name=PGCH/>
| IDLH = 1100 ppm<ref name=PGCH/>
}}
}}
| Section8 = {{Chembox Related
| Section5 = {{Chembox Related
| OtherFunction_label = alkanes
| Function = [[alkane]]s
| OtherFunctn = [[Pentane]]<br />[[Heptane]]
| OtherFunction = {{Unbulleted list|[[Pentane]]|[[Heptane]]}}
| OtherCpds = [[Cyclohexane]]
}}
}}
| Section6 =
}}
}}
'''Hexane''' is a [[hydrocarbon]] with the [[chemical formula]] C<sub>6</sub>H<sub>14</sub>; that is, an [[alkane]] with six [[carbon]] atoms.
'''Hexane''' ({{IPAc-en|ˈ|h|ɛ|k|s|eɪ|n}}) or '''''n''-hexane''' is an [[organic compound]], a straight-chain [[alkane]] with six [[carbon]] atoms and the [[molecular formula]] C<sub>6</sub>H<sub>14</sub>.<ref>{{Cite web |last=PubChem |title=n-HEXANE |url=https://pubchem.ncbi.nlm.nih.gov/compound/8058 |access-date=2023-11-03 |website=pubchem.ncbi.nlm.nih.gov |language=en}}</ref>


Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately {{Convert|69|C}}. It is widely used as a cheap, relatively safe, largely unreactive, and easily evaporated [[non-polar solvent]], and modern [[gasoline]] blends contain about 3% hexane.<ref>{{cite web |title=n-Hexane - Hazardous Agents |url=https://haz-map.com/Agents/105 |website=Haz-Map |access-date=7 July 2022}}</ref>
The term may refer to any of four other [[structural isomer]]s with that formula, or to a mixture of them:<ref>{{cite web|url=http://members.optushome.com.au/scottsoftb/skeletons2.htm|title=C5 and C6 alkanes|publisher=A and B Scott Organic Chemistry|accessdate=2007-10-30}}</ref>. In the [[International Union of Pure and Applied Chemistry|IUPAC]] nomenclature, however, '''hexane''' is the unbranched isomer (''n''-hexane); the other four structures are named as [[methyl group|methyl]]ated 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|2-methylhexane]] C<sub>7</sub>H<sub>16</sub>, which is also called "isoheptane".


The term '''hexanes''' refers to a [[mixture]], composed largely (>60%) of ''n''-hexane, with varying amounts of the isomeric compounds [[2-methylpentane]] and [[3-methylpentane]], and possibly, smaller amounts of nonisomeric C<sub>5</sub>, C<sub>6</sub>, and C<sub>7</sub> (cyclo)alkanes. These "hexanes" mixtures are cheaper than pure hexane and are often used in large-scale operations not requiring a single [[isomer]] (e.g., as cleaning solvent or for [[chromatography]]).
Hexanes are significant constituents of [[gasoline]]. They are all colorless liquids at room temperature, with boiling points between 50 and 70 °C, with gasoline-like odor. They are widely used as cheap, relatively safe, largely unreactive, and easily evaporated [[chemical polarity|non-polar]] [[solvent]]s.


== Uses ==
==Isomers==
{{main|C6H14}}
{| class="wikitable" style="text-align:center;"
|-
! Common name
! IUPAC name
! Text formula
! Skeletal formula
|-
| '''Normal hexane''',<br />'''''n''-Hexane'''
| '''Hexane'''
| CH<sub>3</sub>(CH<sub>2</sub>)<sub>4</sub>CH<sub>3</sub>
| [[File:Hexane-2D-Skeletal.svg|150px]]
|-
| '''Isohexane'''
| '''[[2-Methylpentane]]'''
| (CH<sub>3</sub>)<sub>2</sub>CH(CH<sub>2</sub>)<sub>2</sub>CH<sub>3</sub>
| [[File:2-metilpentāns.svg|110px]]
|-
|
| '''[[3-Methylpentane]]'''
| CH<sub>3</sub>CH<sub>2</sub>CH(CH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub>
| [[File:3-metilpentāns.svg|110px]]
|-
|
| '''[[2,3-Dimethylbutane]]'''
| (CH<sub>3</sub>)<sub>2</sub>CHCH(CH<sub>3</sub>)<sub>2</sub>
| [[File:2,3-dimetilbutāns.svg|90px]]
|-
| '''Neohexane'''
| '''[[2,2-Dimethylbutane]]'''
| (CH<sub>3</sub>)<sub>3</sub>CCH<sub>2</sub>CH<sub>3</sub>
| [[File:2,2-dimetilbutāns.svg|90px]]
|}


==Uses==
In the industry, hexanes are used in the formulation of [[adhesive|glue]]s for shoes, leather products, and roofing. They are also used to extract [[cooking oil]]s from seeds, for cleansing and degreasing all sorts of items, and in textile manufacturing.
In industry, hexanes are used in the formulation of [[adhesive|glue]]s for shoes, [[leather]] products, and roofing. They are also used to extract [[cooking oil]]s (such as [[canola oil]] or [[soybean oil]]) from seeds, for cleansing and [[degreasing]] a variety of items, and in textile manufacturing.


A typical laboratory use of hexanes to extract [[petroleum|oil]] and [[grease (lubricant)|grease]] contaminants from water and soil for analysis.<ref>Use of ozone depleting substances in laboratories. TemaNord 2003:516. http://www.norden.org/pub/ebook/2003-516.pdf</ref>. Since hexane cannot be [[protonation|deprotonated]], it is used in the laboratory for reactions that involve very strong bases, such as the preparation of [[Grignard reaction|Grignard reagent]]s.
A typical laboratory use of hexanes is to extract [[petroleum|oil]] and [[grease (lubricant)|grease]] contaminants from water and soil for analysis.<ref>{{cite book | title=Use of ozone depleting substances in laboratories | publisher=Nordisk Ministerråd | publication-place=Kbh | year=2003 | isbn=92-893-0884-2 | oclc=474188215 | url=http://www.norden.org/en/publications/publikationer/2003-516| archive-url=https://web.archive.org/web/20120716192552/http://www.norden.org/en/publications/publikationer/2003-516 | archive-date=16 July 2012 }}</ref> Since hexane cannot be easily [[deprotonation|deprotonated]], it is used in the laboratory for reactions that involve very strong bases, such as the preparation of [[Organolithium reagent|organolithium]]s. For example, butyllithiums are typically supplied as a hexane solution.<ref>{{Cite journal|last1=Schwindeman|first1=James A.|last2=Woltermann|first2=Chris J.|last3=Letchford|first3=Robert J.|date=2002-05-01|title=Safe handling of organolithium compounds in the laboratory|url=https://pubs.acs.org/doi/full/10.1016/S1074-9098(02)00295-2|journal=Chemical Health & Safety|volume=9|issue=3|pages=6–11|doi=10.1016/s1074-9098(02)00295-2|issn=1074-9098}}</ref>


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.
== Production ==


As an [[internal combustion engine]] fuel, n-hexane has low research and motor [[Octane rating|octane numbers]] of 25 and 26 respectively.<ref>{{Cite journal |last=Al Ibrahim |first=Emad |last2=Farooq |first2=Aamir |date=2020-01-16 |title=Octane Prediction from Infrared Spectroscopic Data |url=https://repository.kaust.edu.sa/handle/10754/660233 |journal=Energy & Fuels |volume=34 |issue=1 |pages=817–826 |doi=10.1021/acs.energyfuels.9b02816 |issn=0887-0624}}</ref> In 1983 its share in Japanese gasoline varied around 6%,<ref>{{Cite journal |last=Ikeda |first=Masayuki |last2=Kumai |first2=Miho |last3=Watanabe |first3=Takao |last4=Fujita |first4=Hiroyoshi |date=1984 |title=Aromatic and Other Contents in Automobile Gasoline in Japan |url=https://www.jstage.jst.go.jp/article/indhealth1963/22/4/22_4_235/_article/-char/ja/ |journal=Industrial health |volume=22 |issue=4 |pages=235–241 |doi=10.2486/indhealth.22.235}}</ref> in 1992 it was present in American gas between 1 and 3%,<ref>{{Cite journal |last=Doskey |first=Paul V. |last2=Porter |first2=Joseph A. |last3=Scheff |first3=Peter A. |date=November 1992 |title=Source Fingerprints for Volatile Non-Methane Hydrocarbons |url=https://www.tandfonline.com/doi/full/10.1080/10473289.1992.10467090 |journal=Journal of the Air & Waste Management Association |language=en |volume=42 |issue=11 |pages=1437–1445 |doi=10.1080/10473289.1992.10467090 |issn=1047-3289}}</ref> and in Swedish automobile fuel in the same year the share was consistently under 2%, often below 1%.<ref>{{Cite journal |last=Östermark |first=Ulf |last2=Petersson |first2=Göran |date=1992-09-01 |title=Assessment of hydrocarbons in vapours of conventional and alkylate-based petrol |url=https://publications.lib.chalmers.se/records/fulltext/local_72590.pdf |journal=Chemosphere |volume=25 |issue=6 |pages=763–768 |doi=10.1016/0045-6535(92)90066-Z |issn=0045-6535}}</ref> By 2011 its share in US gas stood between 1 and 7%.<ref>{{cite web |date=2011 |title=Hydrocarbon Composition of Gasoline Vapor Emissions from Enclosed Fuel Tanks |url=https://nepis.epa.gov/Exe/ZyPURL.cgi?Dockey=P100GPED.TXT |website=nepis.epa.gov |publisher=United States Environmental Protection Agency}}</ref>
Hexanes are chiefly obtained by the [[oil refinery|refining]] of [[petroleum|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&nbsp;°[[Celsius|C]].


==Production==
== Physical properties ==
Hexane is chiefly obtained by [[oil refinery|refining]] [[petroleum|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.<ref>{{Cite journal |last1=Le Van Mao |first1=R. |last2=Melancon |first2=S. |last3=Gauthier-Campbell |first3=C. |last4=Kletnieks |first4=P. |date=2001-05-01 |title=Selective deep catalytic cracking process (SDCC) of petroleum feedstocks for the production of light olefins. I. The Catlever effect obtained with a two reaction-zones system on the conversion of n-hexane |url=https://doi.org/10.1023/A:1016685523095 |journal=Catalysis Letters |language=en |volume=73 |issue=2 |pages=181–186 |doi=10.1023/A:1016685523095 |s2cid=98167823 |issn=1572-879X}}</ref> The industrial product (usually around 50% by weight of the straight-chain isomer) is the fraction boiling at {{Convert|65|-|70|C}}.


==Physical properties==
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.<ref name="mccain"> William D. McCain (1990), [http://books.google.com/books?id=1TJQ64JN2ZUC&printsec=frontcover ''The properties of petroleum fluids'']. PennWell. ISBN 0878143351</ref>
All alkanes are colorless.<ref>{{cite web |url=http://nsdl.niscair.res.in/bitstream/123456789/777/1/Revised+organic+chemistry.pdf |title=Organic Chemistry-I |publisher=Nsdl.niscair.res.in |access-date=2014-02-17 |url-status=dead |archive-url=https://web.archive.org/web/20131029192647/http://nsdl.niscair.res.in/bitstream/123456789/777/1/Revised+organic+chemistry.pdf |archive-date=29 October 2013}}</ref><ref>{{cite web |url=http://textbook.s-anand.net/ncert/class-11/chemistry/13-hydrocarbons |title=13. Hydrocarbons &#124; Textbooks |publisher=Textbook.s-anand.net |access-date=2014-02-17 |url-status=dead |archive-url=https://web.archive.org/web/20141006090735/http://textbook.s-anand.net/ncert/class-11/chemistry/13-hydrocarbons |archive-date=6 October 2014}}</ref> 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.<ref name="mccain">{{cite book | author = William D. McCain | date = 1990 | url = https://books.google.com/books?id=1TJQ64JN2ZUC | title = The properties of petroleum fluids | publisher = PennWell | isbn = 978-0-87814-335-1}}</ref>


{| class="wikitable" style="text-align:center"
{| class="wikitable" style="text-align:center"
|-
!Isomer
!Isomer


!M. P. (°C.)
![[Melting point|M.P.]] (°C)
!M.P. (°F)

!B. P. (°C.)
![[Boiling point|B.P.]] (°C)
!B.P. (°F)
|-
|-
| n-hexane || −95.3 || 68.7
| ''n''-hexane || {{convert|−95.3|C|disp=table}} || {{convert|68.7|C|disp=table}}
|-
|-
| 3-methylpentane || −118.0 || 63.3
| 3-methylpentane|| {{convert|−118.0|C|disp=table}} || {{convert|63.3|C|disp=table}}
|-
|-
| 2-methylpentane (isohexane) || −153.7 || 60.3
| 2-methylpentane (isohexane) || {{convert|−153.7|C|disp=table}} || {{convert|60.3|C|disp=table}}
|-
|-
| 2,3-dimethylbutane || −128.6 || 58.0
| 2,3-dimethylbutane || {{convert|−128.6|C|disp=table}} || {{convert|58.0|C|disp=table}}
|-
|-
| 2,2-dimethylbutane (neohexane) || −99.8 || 49.7
| 2,2-dimethylbutane (neohexane) || {{convert|−99.8|C|disp=table}} || {{convert|49.7|C|disp=table}}
|}
|}


Normal hexane has considerable vapor pressure at room temperatures<ref>[http://www.xydatasource.com/xy-showdatasetpage.php?datasetcode=84114&dsid=63Hexane vapor pressure]</ref>:
Hexane has considerable [[vapor pressure]] at room temperature:


{| class="wikitable" style="text-align: center"
{| class="wikitable" style="text-align: center"
! temperature (°C)
! vapor pressure (mmHg)
|-
|-
! Temperature (°C)
| −40 || 3.36
! Temperature (°F)
! Vapor pressure ([[mmHg]])
! Vapor pressure ([[kPa]])
|-
|-
| {{convert|−40|C|disp=table}} || {{convert|3.36|mmHg|disp=table}}
| −30 || 7.12
|-
|-
| {{convert|−30|C|disp=table}} || {{convert|7.12|mmHg|disp=table}}
| −20 || 14.01
|-
|-
| {{convert|−20|C|disp=table}} || {{convert|14.01|mmHg|disp=table}}
| −10 || 25.91
|-
|-
| {{convert|−10|C|disp=table}} || {{convert|25.91|mmHg|disp=table}}
| 0 || 45.37
|-
|-
| {{convert|0|C|disp=table}} || {{convert|45.37|mmHg|disp=table}}
| 10 || 75.74
|-
|-
| {{convert|10|C|disp=table}} || {{convert|75.74|mmHg|disp=table}}
| 20 || 121.26
|-
|-
| {{convert|20|C|disp=table}} || {{convert|121.26|mmHg|disp=table}}
| 25 || 151.28
|-
|-
| {{convert|25|C|disp=table}} || {{convert|151.28|mmHg|disp=table}}
| 30 || 187.11
|-
|-
| {{convert|30|C|disp=table}} || {{convert|187.11|mmHg|disp=table}}
| 40 || 279.42
|-
|-
| {{convert|40|C|disp=table}} || {{convert|279.42|mmHg|disp=table}}
| 50 || 405.31
|-
|-
| {{convert|50|C|disp=table}} || {{convert|405.31|mmHg|disp=table}}
| 60 || 572.76
|}

== Isomers ==

{| class="wikitable" border="1" style="text-align: center"
|-
|-
| {{convert|60|C|disp=table}} || {{convert|572.76|mmHg|disp=table}}
! Common name
! IUPAC name
! Text formula
! Skeletal formula
|-
| '''normal hexane'''<Br/>'''''N''-hexane'''
| '''hexane'''
| CH<sub>3</sub>(CH<sub>2</sub>)<sub>3</sub>CH<sub>3</sub>
| [[File:Hexane-2D-Skeletal.svg|150px]]
|-
| '''isohexane'''
| '''[[2-Methylpentane|2-methylpentane]]'''
| (CH<sub>3</sub>)<sub>2</sub>CH(CH<sub>2</sub>)<sub>2</sub>CH<sub>3</sub>
| [[File:2-metilpentāns.svg|110px]]
|-
|
| '''[[3-Methylpentane|3-methylpentane]]'''
| CH<sub>3</sub>CH<sub>2</sub>CH(CH<sub>3</sub>)CH<sub>2</sub>CH<sub>3</sub>
| [[File:3-metilpentāns.svg|110px]]
|-
|
| '''[[2,3-Dimethylbutane|2,3-dimethylbutane]]'''
| CH<sub>3</sub>CH(CH<sub>3</sub>)CH(CH<sub>3</sub>)CH<sub>3</sub>
| [[File:2,3-dimetilbutāns.svg|90px]]
|-
| '''neohexane'''
| '''[[2,2-Dimethylbutane|2,2-dimethylbutane]]'''
| CH<sub>3</sub>C(CH<sub>3</sub>)<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub>
| [[File:2,2-dimetilbutāns.svg|90px]]
|}
|}


== Toxicity ==
==Reactivity==
Like most alkanes, hexanes characteristically exhibit 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.<ref>{{OrgSynth|author=Koch, H.|author2=Haaf, W.|title=1-Adamantanecarboxylic Acid|year=1973|collvol=5|collvolpages=20|prep=cv5p0020}}</ref>


== Safety ==
The acute [[toxicity]] of hexane<!-- WHICH ONE? --> is relatively low, although it is a mild [[anesthetic]]. Inhalation of high concentrations produces first a state of mild [[Euphoria (emotion)|euphoria]], followed by [[somnolence]] with [[headache]]s and [[nausea]].
Inhalation of ''n''-hexane at 5000&nbsp;ppm for 10&nbsp;minutes produces marked vertigo; 2500-1000&nbsp;ppm for 12 hours produces [[drowsiness]], [[Fatigue (medical)|fatigue]], loss of appetite, and [[paresthesia]] in the distal extremities; 2500–5000&nbsp;ppm produces muscle weakness, cold pulsation in the extremities, blurred vision, [[headache]], and [[Anorexia (symptom)|anorexia]].<ref>{{cite web|url=http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+91|publisher=[[National Library of Medicine]]|work=Toxicology data network Hazardous Substances Data Bank|title=N-HEXANE|url-status=live|archive-url=https://web.archive.org/web/20150904103024/http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+91|archive-date=4 September 2015}}</ref> Chronic occupational exposure to elevated levels of ''n''-hexane has been demonstrated to be associated with [[peripheral neuropathy]] in [[Auto mechanic|auto mechanics]] in the US, and [[neurotoxicity]] in workers in printing presses, and shoe and furniture factories in Asia, Europe, and North America.<ref>{{Cite journal|last=Centers for Disease Control and Prevention (CDC)|date=2001-11-16|title=n-Hexane-related peripheral neuropathy among automotive technicians--California, 1999-2000|journal=MMWR. Morbidity and Mortality Weekly Report|volume=50|issue=45|pages=1011–1013|issn=0149-2195|pmid=11724159}}</ref>


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 ({{Convert|350|mg/m3|abbr=on}}) over an 8-hour workday.<ref>{{Cite web|title = CDC – NIOSH Pocket Guide to Chemical Hazards – Hexane isomers (excluding n-Hexane)|url = https://www.cdc.gov/niosh/npg/npgd0323.html|work = cdc.gov|access-date = 2015-11-03|url-status = live|archive-url = https://web.archive.org/web/20151031004609/http://www.cdc.gov/niosh/npg/npgd0323.html|archive-date = 31 October 2015}}</ref> However, for ''n''-hexane, the current NIOSH REL is 50 ppm ({{Convert|180|mg/m3|abbr=on|}}) over an 8-hour workday.<ref name=":0">{{Cite web|title=n-Hexane|url=https://www.cdc.gov/niosh/npg/npgd0322.html|last=CDC|date=2018-03-28|website=Centers for Disease Control and Prevention|language=en-us|access-date=2020-05-03}}</ref> 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.<ref>{{Cite web|title=Appendix G: 1989 Air Contaminants Update Project - Exposure Limits NOT in Effect|url=https://www.cdc.gov/niosh/npg/nengapdxg.html|date=2020-02-20|website=www.cdc.gov|language=en-us|access-date=2020-05-03}}</ref> The current n-hexane PEL in the US is 500 ppm ({{Convert|1800|mg/m3|abbr=on|}}).<ref name=":0" />
The long-term [[toxicity]] of ''n''-hexane in humans is well known<ref>{{cite journal
| author = Hathaway GJ, Proctor NH, Hughes JP, and Fischman M
| journal = Proctor and Hughes' chemical hazards of the workplace. 3rd ed. New York, NY: Van Nostrand Reinhold
| volume =
| title =
| issue =
| pages =
| year = 1991
| doi =}}</ref> [[polyneuropathy|Extensive peripheral nervous system failure]] is known to occur in humans chronically exposed to levels of ''n''-hexane ranging from 400 to 600 ppm, with occasional exposures up to 2,500 ppm. The initial symptoms are tingling and cramps in the arms and legs, followed by general muscular weakness. In severe cases, [[atrophy]] of the [[skeletal muscle]]s is observed, along with a loss of coordination and problems of vision. Similar symptoms are observed in animal models. They are associated with a degeneration of the [[peripheral nervous system]] (and eventually the [[central nervous system]]), starting with the distal portions of the longer and wider nerve [[axon]]s.. The toxicity is not due to hexane itself but to one of its [[metabolite]]s, [[hexane-2,5-dione]]. It is believed that this reacts with the [[amino group]] of the [[side chain]] of [[lysine]] residues in [[protein]]s, causing [[cross-link]]ing and a loss of protein function.


Hexane and other volatile hydrocarbons ([[petroleum ether]]) present an [[Aspiration pneumonia|aspiration]] risk.<ref>{{citation | author=Gad, Shayne C | contribution=Petroleum Hydrocarbons | title=Encyclopedia of Toxicology | edition=2nd | volume=3 | publisher=Elsevier | year=2005 | pages=377–379}}</ref> ''n''-Hexane is sometimes used as a [[Denaturation (food)|denaturant]] for alcohol, and as a cleaning agent in the [[textile]], [[furniture]], and leather industries. It is slowly being replaced with other solvents.<ref name="tox">{{cite book | author=Clough, Stephen R | author2=Mulholland, Leyna | contribution=Hexane | title=Encyclopedia of Toxicology | volume=2 | edition=2nd | year=2005 | publisher=Elsevier | pages=522–525}}</ref>
Chronic intoxication from hexane has been observed in [[Inhalant|recreational solvent abusers]] and in workers in the [[shoe]] manufacturing, furniture [[Refurbishment|restoration]] and [[automobile]] construction industries.


Like gasoline, hexane is highly volatile and is an explosion risk. The 1981 [[Louisville sewer explosions]], which destroyed over {{cvt|13|mi|km}} of sewer lines and streets in Kentucky, were caused by ignition of hexane vapors which had been illegally discharged from a [[soybean]] processing plant owned by [[Ralston-Purina]]. Hexane was attributed as the cause of an explosion that occurred in the [[National University of Río Cuarto]], Argentina on 5 December 2007, due to a hexane spill near a heat-producing machine that exploded, producing a fire that killed one student and injured 24 more.
In 1994, ''n''-hexane was included in the list of chemicals on the US Toxic Release Inventory (TRI).<ref name="nfc">
{{cite web|url=http://www.nsc.org/ehc/chemical/N-Hexane.htm|title=N-Hexane Chemical Backgrounder|publisher=National Safety Council|dateformat=dmy|accessdate=25 May 2007}}
</ref> In 2001, the U.S. Environmental Protection Agency issued regulations on the control of emissions of hexane gas due to its potential carcinogenic properties and environmental concerns.<ref name="ncfer">
{{cite web|url=http://es.epa.gov/ncer/publications/meetings/10_26_05/abstracts/do.html|title=Nanostructured Microemulsions as Alternative Solvents to VOCs in Cleaning Technologies and Vegetable Oil Extraction|author=Anuradee Witthayapanyanon and Linh Do|publisher=National Center For Environmental Research|dateformat=dmy|accessdate=25 May 2007}}
</ref>


===Incidents===
The adverse health effects above seem specific to ''n''-hexane; they are much reduced or absent for other isomers. Therefore, the food oil extraction industry, which relied heavily on hexane, has been considering switching to other solvents, including isohexane.<ref name="Wan">Peter J. Wan, Phillip J. Wakelyn (1997), [http://books.google.co.uk/books?id=jqUjKBplqPcC&lpg=PP1&pg=PA189 ''Technology and solvents for extracting oilseeds and nonpetroleum oils''] The American Oil Chemists Society. ISBN 0935315810, p. 189</ref><ref name="newsol">
[[Occupational safety and health|Occupational]] hexane poisoning has occurred with Japanese sandal workers, Italian shoe workers,<ref>{{Cite journal| pmid = 6249607| year = 1980| last1 = Rizzuto| first1 = N| title = N-hexane polyneuropathy. An occupational disease of shoemakers| journal = European Neurology| volume = 19| issue = 5| pages = 308–15| last2 = De Grandis| first2 = D| last3 = Di Trapani| first3 = G| last4 = Pasinato| first4 = E| doi = 10.1159/000115166}}</ref> Taiwan press proofing workers, and others.<ref>{{citation | title=n-Hexane | series=[[Environmental Health Criteria]] | issue=122 | publisher=World Health Organization | year=1991 | url=http://www.inchem.org/documents/ehc/ehc/ehc122.htm | url-status=live | archive-url=https://web.archive.org/web/20140319105541/http://www.inchem.org/documents/ehc/ehc/ehc122.htm | archive-date=19 March 2014}}</ref> Analysis of Taiwanese workers has shown occupational exposure to substances including ''n''-hexane.<ref>{{Cite journal | doi = 10.5491/SHAW.2012.3.4.257| pmid = 23251841|pmc=3521924| title = Occupational Neurotoxic Diseases in Taiwan| journal = Safety and Health at Work| volume = 3| issue = 4| pages = 257–67| year = 2012| last1 = Liu | first1 = C. H. | last2 = Huang | first2 = C. Y. | last3 = Huang | first3 = C. C. }}</ref> In 2010–2011, Chinese workers manufacturing iPhones were reported to have suffered hexane poisoning.<ref>{{cite web |url=http://www.abc.net.au/news/stories/2010/10/26/3048024.htm |title=Workers poisoned while making iPhones – ABC News (Australian Broadcasting Corporation) |publisher=Australian Broadcasting Corporation|date=2010-10-26 |access-date=2015-03-17 |url-status=live |archive-url=https://web.archive.org/web/20110408171509/http://www.abc.net.au/news/stories/2010/10/26/3048024.htm |archive-date=8 April 2011}}</ref><ref>{{cite news|url=https://www.nytimes.com/2011/02/23/technology/23apple.html?pagewanted=all|title=Workers Sickened at Apple Supplier in China|newspaper=The New York Times|date=22 February 2011|author=David Barboza|access-date=2015-03-17|url-status=live|archive-url=https://web.archive.org/web/20150407173034/http://www.nytimes.com/2011/02/23/technology/23apple.html?pagewanted=all|archive-date=7 April 2015}}</ref>
USDA (1996), [http://www.ars.usda.gov/is/AR/archive/aug96/solvent0896.htm?pf=1 Isohexane—New Solvent for Cottonseed Oil Processing]
</ref><ref name="undefined">Yuichiro Ono, Yasuhiro Takeuchi, and Naomi Hisanaga (1981), ''A comparative study on the toxicity of n-hexane and its isomers on the peripheral nerve''. International Archives of Occupational and Environmental Health, volume 48, issue 3, pp. 289–294 {{doi|10.1007/BF00405616}}
</ref>


===Biotransformation===
In the latter part of the 20th and early part of the 21st centuries, a number of explosions have been attributed to the combustion of hexane gas.{{Citation needed|date=November 2009}}
''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 [[neurotoxicity|neurotoxic]] and produces a [[polyneuropathy]].<ref name="tox"/> In view of this behavior, replacement of ''n''-hexane as a solvent has been discussed. [[heptane|''n''-Heptane]] is a possible alternative.<ref>{{cite book | date = 1996 | volume = 387 | pages = 411–427 |vauthors=Filser JG, Csanády GA, Dietz W, Kessler W, Kreuzer PE, Richter M, Störmer A | title = Biological Reactive Intermediates V | chapter = 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 | pmid=8794236| doi = 10.1007/978-1-4757-9480-9_50 | series = Advances in Experimental Medicine and Biology | isbn = 978-1-4757-9482-3 }}</ref>


== See also ==
==See also==
*[[Cyclohexane]]
*[[Perfluorohexane]]


==References==
* [[Cyclohexane]]
{{Reflist|colwidth=30em}}
* [[Hexene]]

== References ==
{{reflist|2}}

== External links ==

* [http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/_icsc02/icsc0279.htm International Chemical Safety Card 0279] (''n''-hexane)
* [http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/_icsc12/icsc1262.htm International Chemical Safety Card 1262] (2-methylpentane)
* [http://physchem.ox.ac.uk/MSDS/HE/hexane.html Material Safety Data Sheet for Hexane]
* [http://www.npi.gov.au/database/substance-info/profiles/47.html National Pollutant Inventory - ''n''-hexane fact sheet]


==External links==
*[http://www.inchem.org/documents/icsc/icsc/eics1262.htm International Chemical Safety Card 1262] (2-methylpentane)
*[https://web.archive.org/web/20071025061540/http://physchem.ox.ac.uk/MSDS/HE/hexane.html Material Safety Data Sheet for Hexane]
*[https://web.archive.org/web/20090912082512/http://www.npi.gov.au/database/substance-info/profiles/47.html National Pollutant Inventory – ''n''-hexane fact sheet]
<!-- *[http://www.nsc.org/library/chemical/N-Hexane.htm National Safety Council] broken link -->
<!-- *[http://www.nsc.org/library/chemical/N-Hexane.htm National Safety Council] broken link -->
*[https://web.archive.org/web/20150904103023/http://www.ars-grin.gov/cgi-bin/duke/chemical.pl?HEXANE Phytochemica l database entry]

* [http://www.cdc.gov/niosh/npg/npgd0323.html NIOSH Pocket Guide to Chemical Hazards] (hexane isomers)
*[https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5045a3.htm Center for Disease Control and Prevention]
* [http://www.ars-grin.gov/cgi-bin/duke/chemical.pl?HEXANE Phytochemica l database entry]
* [http://www.cdc.gov/mmwr/preview/mmwrhtml/mm5045a3.htm Center for Disease Control and Prevention]

<!-- *[http://www.nsc.org/ehc/chemical/N-Hexane.htm National Safety Council] this link already exists in references -->
<!-- *[http://www.nsc.org/ehc/chemical/N-Hexane.htm National Safety Council] this link already exists in references -->
*[https://web.archive.org/web/20071013111049/http://nsc.org/EHC/jrn/tips/tip167.htm Warning from National Safety Council "COMMON CHEMICAL AFFECTS AUTO MECHANICS"]
*Australian [https://web.archive.org/web/20090912082512/http://www.npi.gov.au/database/substance-info/profiles/47.html National Pollutant Inventory (NPI)] page
*[http://www.epa.gov/ttn/atw/vegoil/fr12ap01.pdf "EPA does not consider n-hexane classifiable as a human carcinogen."] Federal Register / Vol. 66, No. 71 / Thursday, 12 April 2001 / Rules and Regulations


{{Alkanes}}
* [http://www.nsc.org/EHC/jrn/tips/tip167.htm Warning from National Safety Council "COMMON CHEMICAL AFFECTS AUTO MECHANICS"]
{{Hydrides by group}}
* Australian [http://www.npi.gov.au/database/substance-info/profiles/47.html National Pollutant Inventory (NPI)] page
* [http://www.epa.gov/ttn/atw/vegoil/fr12ap01.pdf "EPA does not consider n-hexane classifiable as a human carcinogen."] Federal Register / Vol. 66, No. 71 / Thursday, April 12, 2001 / Rules and Regulations


{{authority control}}
{{alkanes}}


[[Category:Alkanes]]
[[Category:Alkanes]]
[[Category:Hazardous air pollutants]]
[[Category:Hazardous air pollutants]]
[[Category:Hydrocarbon solvents]]
[[Category:Hydrocarbon solvents]]
[[Category:Commodity chemicals]]

[[ar:هكسان]]
[[bs:Heksan]]
[[ca:Hexà]]
[[cs:Hexan]]
[[da:Hexan]]
[[de:Hexan]]
[[et:Heksaan]]
[[el:Εξάνιο]]
[[es:Hexano]]
[[eo:Heksano]]
[[fr:Hexane]]
[[ko:헥세인]]
[[hi:हेक्सेन]]
[[hr:Heksan]]
[[id:Heksana]]
[[it:Esano]]
[[he:הקסאן]]
[[ku:Heksan]]
[[lv:Heksāns]]
[[hu:Hexán]]
[[ms:Heksana]]
[[nl:N-hexaan]]
[[ja:ヘキサン]]
[[no:Heksan]]
[[pl:Heksan]]
[[pt:Hexano]]
[[ru:Гексан]]
[[cu:Гєѯанъ]]
[[sr:Хексан]]
[[fi:Heksaani]]
[[sv:Hexan]]
[[ta:ஹெக்சேன்]]
[[th:เฮกเซน]]
[[tr:Hekzan]]
[[uk:Гексан]]
[[vi:Hexan]]
[[zh:己烷]]

Latest revision as of 17:16, 19 December 2024

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
Names
Preferred IUPAC name
Hexane[2]
Other names
Sextane,[1] hexacarbane
Identifiers
3D model (JSmol)
1730733
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.003.435 Edit this at Wikidata
EC Number
  • 203-777-6
1985
KEGG
MeSH n-hexane
RTECS number
  • MN9275000
UNII
UN number 1208
  • InChI=1S/C6H14/c1-3-5-6-4-2/h3-6H2,1-2H3 checkY
    Key: VLKZOEOYAKHREP-UHFFFAOYSA-N checkY
  • CCCCCC
Properties
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
9.5 mg L−1
log P 3.764
Vapor pressure 17.60 kPa (at 20.0 °C)
7.6 nmol Pa−1 kg−1
UV-vis (λmax) 200 nm
−74.6·10−6 cm3/mol
1.375
Viscosity 0.3 mPa·s
0.08 D
Thermochemistry
265.2 J K−1 mol−1
296.06 J K−1 mol−1
−199.4–−198.0 kJ mol−1
−4180–−4140 kJ mol−1
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Reproductive toxicity – After aspiration, pulmonary oedema, pneumonitis[4]
GHS labelling:
GHS02: Flammable GHS07: Exclamation mark GHS08: Health hazard GHS09: Environmental hazard
Danger
H225, H302, H305, H315, H336, H361fd, H373, H411
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)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 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. gasolineInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
3
0
Flash point −26.0 °C (−14.8 °F; 247.2 K)
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)[6]
56137 mg/kg (rat, oral)[6]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 500 ppm (1800 mg/m3)[5]
REL (Recommended)
 TWA 50 ppm (180 mg/m3)[5]
IDLH (Immediate danger)
 1100 ppm[5]
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 ?)

Hexane (/ˈhɛkseɪn/) or n-hexane is an organic compound, a straight-chain alkane with six carbon atoms and the molecular formula C6H14.[7]

Hexane is a colorless liquid, odorless when pure, and with a boiling point of approximately 69 °C (156 °F). It is widely used as a cheap, relatively safe, largely unreactive, and easily evaporated non-polar solvent, and modern gasoline blends contain about 3% hexane.[8]

The term hexanes refers to a mixture, composed largely (>60%) of n-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. These "hexanes" mixtures are cheaper than pure hexane and are often used in large-scale operations not requiring a single isomer (e.g., as cleaning solvent or for chromatography).

Isomers

[edit]
Main article: C6H14
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

[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 or soybean 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.[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.

As an internal combustion engine fuel, n-hexane has low research and motor octane numbers of 25 and 26 respectively.[11] In 1983 its share in Japanese gasoline varied around 6%,[12] in 1992 it was present in American gas between 1 and 3%,[13] and in Swedish automobile fuel in the same year the share was consistently under 2%, often below 1%.[14] By 2011 its share in US gas stood between 1 and 7%.[15]

Production

[edit]

Hexane is 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.[16] 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

[edit]

All alkanes are colorless.[17][18] 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.[19]

Isomer M.P. (°C) M.P. (°F) B.P. (°C) B.P. (°F)
n-hexane −95.3 −139.5 68.7 155.7
3-methylpentane −118.0 −180.4 63.3 145.9
2-methylpentane (isohexane) −153.7 −244.7 60.3 140.5
2,3-dimethylbutane −128.6 −199.5 58.0 136.4
2,2-dimethylbutane (neohexane) −99.8 −147.6 49.7 121.5

Hexane has considerable vapor pressure at room temperature:

Temperature (°C) Temperature (°F) Vapor pressure (mmHg) Vapor pressure (kPa)
−40 −40 3.36 0.448
−30 −22 7.12 0.949
−20 −4 14.01 1.868
−10 14 25.91 3.454
0 32 45.37 6.049
10 50 75.74 10.098
20 68 121.26 16.167
25 77 151.28 20.169
30 86 187.11 24.946
40 104 279.42 37.253
50 122 405.31 54.037
60 140 572.76 76.362

Reactivity

[edit]

Like most alkanes, hexanes characteristically exhibit 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.[20]

Safety

[edit]

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.[21] 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.[22]

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.[23] However, for n-hexane, the current NIOSH REL is 50 ppm (180 mg/m3 (0.079 gr/cu ft)) over an 8-hour workday.[24] 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.[25] The current n-hexane PEL in the US is 500 ppm (1,800 mg/m3 (0.79 gr/cu ft)).[24]

Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk.[26] 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.[27]

Like gasoline, hexane is highly volatile and is an explosion risk. The 1981 Louisville sewer explosions, which destroyed over 13 mi (21 km) of sewer lines and streets in Kentucky, were caused by ignition of hexane vapors which had been illegally discharged from a soybean processing plant owned by Ralston-Purina. Hexane was attributed as the cause of an explosion that occurred in the National University of Río Cuarto, Argentina on 5 December 2007, due to a hexane spill near a heat-producing machine that exploded, producing a fire that killed one student and injured 24 more.

Incidents

[edit]

Occupational hexane poisoning has occurred with Japanese sandal workers, Italian shoe workers,[28] Taiwan press proofing workers, and others.[29] Analysis of Taiwanese workers has shown occupational exposure to substances including n-hexane.[30] In 2010–2011, Chinese workers manufacturing iPhones were reported to have suffered hexane poisoning.[31][32]

Biotransformation

[edit]

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.[27] In view of this behavior, replacement of n-hexane as a solvent has been discussed. n-Heptane is a possible alternative.[33]

See also

[edit]

References

[edit]
  1. ^ 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.
  2. ^ "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.
  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. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0322". National Institute for Occupational Safety and Health (NIOSH).
  6. ^ a b "n-Hexane". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  7. ^ PubChem. "n-HEXANE". pubchem.ncbi.nlm.nih.gov. Retrieved 3 November 2023.
  8. ^ "n-Hexane - Hazardous Agents". Haz-Map. Retrieved 7 July 2022.
  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. ^ Al Ibrahim, Emad; Farooq, Aamir (16 January 2020). "Octane Prediction from Infrared Spectroscopic Data". Energy & Fuels. 34 (1): 817–826. doi:10.1021/acs.energyfuels.9b02816. ISSN 0887-0624.
  12. ^ Ikeda, Masayuki; Kumai, Miho; Watanabe, Takao; Fujita, Hiroyoshi (1984). "Aromatic and Other Contents in Automobile Gasoline in Japan". Industrial health. 22 (4): 235–241. doi:10.2486/indhealth.22.235.
  13. ^ Doskey, Paul V.; Porter, Joseph A.; Scheff, Peter A. (November 1992). "Source Fingerprints for Volatile Non-Methane Hydrocarbons". Journal of the Air & Waste Management Association. 42 (11): 1437–1445. doi:10.1080/10473289.1992.10467090. ISSN 1047-3289.
  14. ^ Östermark, Ulf; Petersson, Göran (1 September 1992). "Assessment of hydrocarbons in vapours of conventional and alkylate-based petrol" (PDF). Chemosphere. 25 (6): 763–768. doi:10.1016/0045-6535(92)90066-Z. ISSN 0045-6535.
  15. ^ "Hydrocarbon Composition of Gasoline Vapor Emissions from Enclosed Fuel Tanks". nepis.epa.gov. United States Environmental Protection Agency. 2011.
  16. ^ Le Van Mao, R.; Melancon, S.; Gauthier-Campbell, C.; Kletnieks, P. (1 May 2001). "Selective deep catalytic cracking process (SDCC) of petroleum feedstocks for the production of light olefins. I. The Catlever effect obtained with a two reaction-zones system on the conversion of n-hexane". Catalysis Letters. 73 (2): 181–186. doi:10.1023/A:1016685523095. ISSN 1572-879X. S2CID 98167823.
  17. ^ "Organic Chemistry-I" (PDF). Nsdl.niscair.res.in. Archived from the original (PDF) on 29 October 2013. Retrieved 17 February 2014.
  18. ^ "13. Hydrocarbons | Textbooks". Textbook.s-anand.net. Archived from the original on 6 October 2014. Retrieved 17 February 2014.
  19. ^ William D. McCain (1990). The properties of petroleum fluids. PennWell. ISBN 978-0-87814-335-1.
  20. ^ Koch, H.; Haaf, W. (1973). "1-Adamantanecarboxylic Acid". Organic Syntheses; Collected Volumes, vol. 5, p. 20.
  21. ^ "N-HEXANE". Toxicology data network Hazardous Substances Data Bank. National Library of Medicine. Archived from the original on 4 September 2015.
  22. ^ 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.
  23. ^ "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.
  24. ^ a b CDC (28 March 2018). "n-Hexane". Centers for Disease Control and Prevention. Retrieved 3 May 2020.
  25. ^ "Appendix G: 1989 Air Contaminants Update Project - Exposure Limits NOT in Effect". www.cdc.gov. 20 February 2020. Retrieved 3 May 2020.
  26. ^ Gad, Shayne C (2005), "Petroleum Hydrocarbons", Encyclopedia of Toxicology, vol. 3 (2nd ed.), Elsevier, pp. 377–379
  27. ^ a b Clough, Stephen R; Mulholland, Leyna (2005). "Hexane". Encyclopedia of Toxicology. Vol. 2 (2nd ed.). Elsevier. pp. 522–525.
  28. ^ 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.
  29. ^ n-Hexane, Environmental Health Criteria, World Health Organization, 1991, archived from the original on 19 March 2014
  30. ^ 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.
  31. ^ "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.
  32. ^ 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.
  33. ^ 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". Biological Reactive Intermediates V. Advances in Experimental Medicine and Biology. Vol. 387. pp. 411–427. doi:10.1007/978-1-4757-9480-9_50. ISBN 978-1-4757-9482-3. PMID 8794236.
[edit]
Retrieved from "https://en.wikipedia.org/enwiki/w/index.php?title=Hexane&oldid=1263967881"