Difference between revisions of "Acetone"

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{{chembox
 
{{chembox
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|   Name = Acetone<ref>''Merck Index'', 11th Edition, '''58'''.</ref>
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| Name = Acetone<ref>{{Merck11th|58}}.</ref>
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|   ImageFileL1 = Acetone.svg
+
| ImageFileL1 = Acetone.svg
 
|  ImageSizeL1 = 100px
 
|  ImageSizeL1 = 100px
 
|  ImageNameL1 = Acetone
 
|  ImageNameL1 = Acetone
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|   ImageFileR1 = Acetone-CRC-MW-ED-dimensions-2D.png
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| ImageFileR1 = Acetone-CRC-MW-ED-dimensions-2D.png
 
|  ImageSizeR1 = 150px
 
|  ImageSizeR1 = 150px
 
|  ImageNameR1 = Structure and dimensions of the acetone molecule
 
|  ImageNameR1 = Structure and dimensions of the acetone molecule
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|   ImageFileL2 = Acetone-3D-balls.png
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| ImageFileL2 = Acetone-3D-balls.png
 
|  ImageSizeL2 = 130px
 
|  ImageSizeL2 = 130px
 
|  ImageNameL2 = Ball-and-stick model of acetone
 
|  ImageNameL2 = Ball-and-stick model of acetone
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|   ImageFileR2 = Acetone-3D-vdW.png
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| ImageFileR2 = Acetone-3D-vdW.png
 
|  ImageSizeR2 = 150px
 
|  ImageSizeR2 = 150px
 
|  ImageNameR2 = Space-filling model of acetone
 
|  ImageNameR2 = Space-filling model of acetone
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|   IUPACName = propanone
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| IUPACName = propanone
 
|  OtherNames = β-ketopropane, dimethyl ketone, dimethylformaldehyde, DMK, propanone, 2-propanone, propan-2-one
 
|  OtherNames = β-ketopropane, dimethyl ketone, dimethylformaldehyde, DMK, propanone, 2-propanone, propan-2-one
 
| Section1 = {{Chembox Identifiers
 
| Section1 = {{Chembox Identifiers
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|  SMILES = CC(=O)C
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|  InChI = 1/C3H6O/c1-3(2)4/h1-2H3
−
|  EC = 200-662-2
+
|  StdInChI = 1S/C3H6O/c1-3(2)4/h1-2H3
 +
|  InChIKey = CSCPPACGZOOCGX-UHFFFAOYAF
 +
|  StdInChIKey = CSCPPACGZOOCGX-UHFFFAOYSA-N
 
|  CASNo = 67-64-1
 
|  CASNo = 67-64-1
 
|    CASNo_Ref = {{cascite}}
 
|    CASNo_Ref = {{cascite}}
 +
|  EC-number = 200-662-2
 +
|  ChemSpiderID = 175
 
|  RTECS = AL31500000
 
|  RTECS = AL31500000
−
|  ChemSpiderID = 175
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|  SMILES = CC(=O)C
−
|  InChI=1/C3H6O/c1-3(2)4/h1-2H3
 
 
   }}
 
   }}
 
| Section2 = {{Chembox Properties
 
| Section2 = {{Chembox Properties
 +
|  Reference = <ref name="ICSC">{{ICSC-ref|0087|name=Acetone|date=April 1994}}.</ref>
 
|  C=3|H=6|O=1
 
|  C=3|H=6|O=1
−
|  Appearance = Colorless liquid
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|  Appearance = colorless liquid
 
|  Density = 0.79 g/cm<sup>3</sup>
 
|  Density = 0.79 g/cm<sup>3</sup>
−
|  Solubility = [[miscible]]
+
|  Solubility = miscible
 
|  MeltingPtC = −94.9
 
|  MeltingPtC = −94.9
 
|  BoilingPtC = 56.53
 
|  BoilingPtC = 56.53
−
|  Viscosity = 0.32 c[[Poise|P]] (20 °C)
+
|  Viscosity = 0.32 cP (20 °C)
 
|  pKa = 24.2
 
|  pKa = 24.2
−
|  logP = 0.2
+
|  logP = −0.24
 
|  RefractIndex = 1.359 (20 °C)
 
|  RefractIndex = 1.359 (20 °C)
 +
|  Dipole = 2.91 D
 +
|  VaporPressure = 24 kPa (20 ºC)
 
   }}
 
   }}
 
| Section3 = {{Chembox Structure
 
| Section3 = {{Chembox Structure
 
|  MolShape = trigonal planar at C=O
 
|  MolShape = trigonal planar at C=O
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|  Dipole = 2.91 [[Debye|D]]
 
 
   }}
 
   }}
 
| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
−
|  ExternalMSDS =
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|  Reference = <ref name="ICSC"/><ref>{{CLP Regulation|index=606-001-00-8|page=517}}</ref><ref>{{PGCH-ref|0004|name=Acetone}}.</ref>
−
|  EUClass = {{Hazchem F}}<br />{{Hazchem Xi}}
+
|  ExternalMSDS = {{ICSC-small|0087}}
−
|  NFPA-H = 1
+
|  EUIndex = 606-001-00-8
−
|  NFPA-F = 3
+
|  GHSPictograms = {{GHS02|Flam. Liq. 2}}{{GHS07|Eye Irrit. 2; STOT SE 3}}
−
|  NFPA-R = 0
+
|  GHSSignalWord = DANGER
−
|  RPhrases = {{R11}}, {{R36}}, {{R66}}, {{R67}}
+
|  HPhrases = {{H-phrases|225|319|336}} <!-- also EUH066 in the European Union -->
−
|  SPhrases = {{S2}}, {{S9}}, {{S16}}, {{S26}}
+
|  FlashPt = -18 °C (0 ºF)
−
|  FlashPt = -17 °C
+
|  Autoignition = 465 °C (869 ºF)
−
|  Autoignition = 465 °C
+
|  ExploLimits = 2.2–13%
−
|  ExploLimits = 4.0–57.0
+
|  PEL = 1000 ppm TWA
 
|  LD50 = >2000 mg/kg, oral (rat)
 
|  LD50 = >2000 mg/kg, oral (rat)
 
   }}
 
   }}
 
| Section8 = {{Chembox Related
 
| Section8 = {{Chembox Related
−
|  Function = [[ketone]]s
 
 
|  OtherFunctn = [[Butanone]]
 
|  OtherFunctn = [[Butanone]]
−
|   Function = [[solvent]]s
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|   Function = [[ketone]]s
−
|  OtherFunctn = [[water (molecule)|Water]]<br />[[Ethanol]]<br />[[Isopropanol]]<br />[[Toluene]]
 
 
   }}
 
   }}
 
}}
 
}}
−
'''Acetone''' is the [[organic compound]] with the [[chemical formula|formula]] OC(CH<sub>3</sub>)<sub>2</sub>.  This colorless, mobile, flammable liquid is the simplest example of the [[ketone]]s. Owing to the fact that acetone is [[miscible]] with [[water (molecule)|water]] it serves as an important [[solvent]] in its own right, typically as the solvent of choice for cleaning purposes in the laboratory.  More than 3 million tonnes are produced annually, mainly as a precursor to polymers.<ref name=Ullmann>Stylianos Sifniades, Alan B. Levy, “Acetone” in Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.</ref>  Familiar household uses of acetone are as the active ingredient in [[nail polish remover]] and as paint thinner and sanitary cleaner/nail polish remover base.  It is a common building block in organic chemistry. In addition to being manufactured, acetone also occurs naturally, even being biosynthesized in small amounts in the human body.
+
'''Acetone''' is the [[organic compound]] with the [[chemical formula|formula]] OC(CH<sub>3</sub>)<sub>2</sub>.  This colorless, mobile, flammable liquid is the simplest example of the [[ketone]]s. Owing to the fact that acetone is [[miscible]] with [[water (molecule)|water]] it serves as an important [[solvent]] in its own right, typically as the solvent of choice for cleaning purposes in the laboratory.  More than 3 million tonnes are produced annually, mainly as a precursor to polymers.<ref name="Ullmann">{{Ullmann | first1 = Stylianos | last1 = Sifniades | first2 = Alan B. | last2 = Levy | contribution = Acetone}}.</ref>  Familiar household uses of acetone are as the active ingredient in [[nail polish remover]] and as paint thinner and sanitary cleaner/nail polish remover base.  It is a common building block in organic chemistry. In addition to being manufactured, acetone also occurs naturally, even being biosynthesized in small amounts in the human body.
  
 
==Production==
 
==Production==
 
Acetone is produced directly or indirectly from propene.  Most commonly, in the [[cumene process]], benzene is alkylated with propene and the resulting [[cumene]] (isopropylbenzene) is oxidized to give [[phenol]] and acetone:
 
Acetone is produced directly or indirectly from propene.  Most commonly, in the [[cumene process]], benzene is alkylated with propene and the resulting [[cumene]] (isopropylbenzene) is oxidized to give [[phenol]] and acetone:
 
:C<sub>6</sub>H<sub>5</sub>CH(CH<sub>3</sub>)<sub>2</sub>  +  O<sub>2</sub>  →  C<sub>6</sub>H<sub>5</sub>OH  +  OC(CH<sub>3</sub>)<sub>2</sub>
 
:C<sub>6</sub>H<sub>5</sub>CH(CH<sub>3</sub>)<sub>2</sub>  +  O<sub>2</sub>  →  C<sub>6</sub>H<sub>5</sub>OH  +  OC(CH<sub>3</sub>)<sub>2</sub>
−
This conversion entails the intermediacy of cumene hydroperoxide, C<sub>6</sub>H<sub>5</sub>C(OOH)(CH<sub>3</sub>)<sub>2</sub>.
+
This conversion entails the intermediacy of [[cumene hydroperoxide]], C<sub>6</sub>H<sub>5</sub>C(OOH)(CH<sub>3</sub>)<sub>2</sub>.
  
−
Acetone is also produced by the direct oxidation of propene with a Pd(II)/Cu(II) catalysts, akin to the [[Wacker process]].
+
Acetone is also produced by the direct oxidation of propene with a palladium(II)/copper(II) catalyst, akin to the [[Wacker process]].
  
 
===Older production methods===
 
===Older production methods===
−
Previously, acetone was produced by the [[dry distillation]] of [[acetate]]s, for example [[calcium acetate]]. During [[World War I]] acetone was produced via [[bacterium|bacterial]] [[Fermentation (biochemistry)|fermentation]], as developed by [[Chaim Weizmann]] (later the first president of [[Israel]]) in order to help the British war effort.<ref name=Ullmann/> This [[Clostridium acetobutylicum|Acetone Butanol Ethanol process]] was abandoned due to the small yields.<ref name=Ullmann/>
+
Previously, acetone was produced by the [[dry distillation]] of [[acetate]]s, for example [[calcium acetate]]. During [[World War I]] acetone was produced via [[bacterium|bacterial]] [[Fermentation (biochemistry)|fermentation]], as developed by [[Chaim Weizmann]] (later the first president of [[Israel]]) in order to help the British war effort.<ref name=Ullmann/> This [[Clostridium acetobutylicum|Acetone Butanol Ethanol process]] was abandoned due to the small yields.<ref name="Ullmann"/>
  
 
===Biosynthesis===
 
===Biosynthesis===
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Acetone is a good solvent for most plastics and synthetic fibres including those used in [[Nalgene]] bottles made of polystyrene, polycarbonate and some types of polypropylene.<ref>[http://www.nalgenelabware.com/techdata/chemical/ NALGENE Labware - Technical Data]</ref>. It is ideal for thinning fiberglass resin, cleaning fiberglass tools and dissolving two-part [[epoxy|epoxies]] and [[superglue]] before hardening. It is used as a volatile component of some [[paint]]s and [[varnish]]es.  As a heavy-duty degreaser, it is useful in the preparation of metal prior to painting; it also thins polyester resins, vinyl and adhesives.
 
Acetone is a good solvent for most plastics and synthetic fibres including those used in [[Nalgene]] bottles made of polystyrene, polycarbonate and some types of polypropylene.<ref>[http://www.nalgenelabware.com/techdata/chemical/ NALGENE Labware - Technical Data]</ref>. It is ideal for thinning fiberglass resin, cleaning fiberglass tools and dissolving two-part [[epoxy|epoxies]] and [[superglue]] before hardening. It is used as a volatile component of some [[paint]]s and [[varnish]]es.  As a heavy-duty degreaser, it is useful in the preparation of metal prior to painting; it also thins polyester resins, vinyl and adhesives.
  
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Many millions of kilograms of acetone are consumed in the production of the solvents methyl isobutyl alcohol and [[methyl isobutyl ketone]].  These products arise via an initial [[aldol condensation]] to give [[diacetone alcohol]].<ref name=Ullmann/>
+
Many millions of kilograms of acetone are consumed in the production of the solvents methyl isobutyl alcohol and [[methyl isobutyl ketone]].  These products arise via an initial [[aldol condensation]] to give [[diacetone alcohol]].<ref name="Ullmann"/>
−
:2 (CH<sub>3</sub>)<sub>2</sub>CO   →   (CH<sub>3</sub>)<sub>2</sub>C(OH)CH<sub>2</sub>C(O)CH<sub>3</sub>
+
:2(CH<sub>3</sub>)<sub>2</sub>CO → (CH<sub>3</sub>)<sub>2</sub>C(OH)CH<sub>2</sub>C(O)CH<sub>3</sub>
  
−
Acetone is used as a solvent by the pharmaceutical industry and as a denaturation agent in denatured alcohol.<ref>{{Cite book
+
Acetone is used as a solvent by the pharmaceutical industry and as a denaturation agent in denatured alcohol.<ref>{{Citation | last1 = Weiner | first1 = Myra L. | first2 = Lois A. | last2 = Kotkoskie | title = Excipient Toxicity and Safety | year = 1999 | page = 32 | isbn = 0824782100}}</ref> Acetone is also present as an [[excipient]] in some pharmaceutical products.<ref>{{citation | url = http://www.accessdata.fda.gov/scripts/cder/iig/index.cfm}}.</ref>
−
| isbn = 0824782100, 9780824782108
 
−
| pages = 32
 
−
| last = Weiner
 
−
| first = Myra L.
 
−
| coauthors = Lois A. Kotkoskie
 
−
| title = Excipient Toxicity and Safety
 
−
| date = 1999
 
−
}}</ref> Acetone is also present as an [[excipient]] in some pharmaceutical products.<ref>http://www.accessdata.fda.gov/scripts/cder/iig/index.cfm</ref>
 
  
 
====Storage of acetylene====
 
====Storage of acetylene====
−
Although flammable itself, acetone is also used extensively as a solvent for the safe transporting and storing of [[acetylene]], which cannot be safely pressurized as a pure compound. Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone. One liter of acetone can dissolve around 250 liters of acetylene.<ref>[http://www.msha.gov/alerts/hazardsofacetylene.htm Mine Safety and Health Administration (MSHA) - Safety Hazard Information - Special Hazards of Acetylene]</ref><ref>[http://www.aga.com/web/web2000/com/WPPcom.nsf/pages/History_Acetylene_1 History - Acetylene dissolved in acetone]</ref>
+
Although flammable itself, acetone is also used extensively as a solvent for the safe transporting and storing of [[acetylene]], which cannot be safely pressurized as a pure compound. Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone. One liter of acetone can dissolve around 250&nbsp;liters of acetylene.<ref>{{citation | url = http://www.msha.gov/alerts/hazardsofacetylene.htm | publisher = U.S. Mine Safety and Health Administration (MSHA) | webpage = Safety Hazard Information - Special Hazards of Acetylene}}.</ref><ref>{{citation | url = http://www.aga.com/web/web2000/com/WPPcom.nsf/pages/History_Acetylene_1 | webpage = History - Acetylene dissolved in acetone}}.</ref>
  
 
===Laboratory uses===
 
===Laboratory uses===
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In the laboratory, acetone is used as a [[chemical polarity|polar]] [[aprotic solvent]] in a variety of [[organic reaction]]s, such as [[SN2 reaction|S<sub>N</sub>2 reactions]]. The use of acetone solvent is also critical for the [[Jones oxidation]]. It is a common solvent for rinsing [[laboratory glassware]] because of its low cost, volatility, and ability to dissolve water.  For similar reasons, acetone is also used as a [[desiccant|drying agent]].  Acetone can be cooled with [[dry ice]] to -78 °C without freezing; acetone/dry ice baths are commonly used to conduct reactions at low temperatures.  Acetone is fluorescent under ultraviolet light, and acetone vapor may be used as a fluorescent tracer in fluid flow experiments.<ref>{{cite journal | author = A. Lozano, B. Yip and R. K. Hanson | title = Acetone: a tracer for concentration measurements in gaseous flows by planar laser-induced fluorescence | journal = [[Exp. Fluids]] | volume = 13 | pages = 369–376 | year =  1992 | doi = 10.1007/BF00223244}}</ref>
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In the laboratory, acetone is used as a [[chemical polarity|polar]] [[aprotic solvent]] in a variety of [[organic reaction]]s, such as [[SN2 reaction|S<sub>N</sub>2 reactions]]. The use of acetone solvent is also critical for the [[Jones oxidation]]. It is a common solvent for rinsing [[laboratory glassware]] because of its low cost, volatility, and ability to dissolve water.  For similar reasons, acetone is also used as a [[desiccant|drying agent]].  Acetone can be cooled with [[dry ice]] to -78&nbsp;°C without freezing; acetone/dry ice baths are commonly used to conduct reactions at low temperatures.  Acetone is fluorescent under ultraviolet light, and acetone vapor may be used as a fluorescent tracer in fluid flow experiments.<ref>{{citation | first1 = A. | last1 = Lozano | first2 = B. | last2 = Yip | first3 = R. K. | last3 = Hanson | title = Acetone: a tracer for concentration measurements in gaseous flows by planar laser-induced fluorescence | journal = Exp. Fluids | volume = 13 | pages = 369–76 | year =  1992 | doi = 10.1007/BF00223244}}.</ref>
  
 
===Domestic and other niche uses===
 
===Domestic and other niche uses===
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It can be used as an artistic agent; when rubbed on the back of a laser print or photocopy placed face-down on another surface and burnished firmly, the toner of the image is allowed to transfer to the destination surface.
 
It can be used as an artistic agent; when rubbed on the back of a laser print or photocopy placed face-down on another surface and burnished firmly, the toner of the image is allowed to transfer to the destination surface.
  
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Some automotive enthusiasts add acetone at around 1 part in 500 to their fuel, following claims of dramatic improvement in fuel economy and engine life.<ref>{{cite web|author=Louis LaPonte|url=http://www.brightgreen.us/lubedev/smartgas/additive.htm|title=Acetone in Fuels (A Study of Dimethylketone or Propanone)|accessdate=2007-06-06|date=2007-02-13|publisher=[http://smartgas.net Smartgas.net]}}</ref> This practice is controversial as the body of systematic testing shows that acetone has no measurable effect or may in fact reduce engine life by adversely affecting fuel system parts.<ref>{{cite web|url=http://www.helenair.com/articles/2006/01/21/automotive/c01012106_03.txt|publisher=[[Independent Record]]|date=2006-01-21|title=Click and Clack Talk Cars|author=Tom and Ray Magliozzi|accessdate=2007-06-06}}</ref><ref>{{cite web|url=http://msgboard.snopes.com/message/ultimatebb.php?/ubb/get_topic/f/20/t/000594/p/1.html|title=Can adding Acetone to fuel increase mpg by 15 to 35%?|publisher=[[Snopes|Snopes.com]] Message Board|accessdate=2007-06-06}}</ref> Debates on this subject and the perennial claims of a "Big Oil" cover-up intensified when the practice was addressed on the popular American TV show [[MythBusters]] in 2006, and shown to have negative effect in the televised fuel economy test.<ref>[[MythBusters]] ([[MythBusters (season 4)#Episode 53 - "Exploding Pants"|Season 4, Episode 53]])</ref>
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Some automotive enthusiasts add acetone at around 1&nbsp;part in 500 to their fuel, following claims of dramatic improvement in fuel economy and engine life.<ref>{{citation | first = Louis | last = LaPonte | url=http://www.brightgreen.us/lubedev/smartgas/additive.htm | webpage = Acetone in Fuels (A Study of Dimethylketone or Propanone) | accessdate=2007-06-06 | date = February 2007 | website = Smartgas.net}}.</ref> This practice is controversial as the body of systematic testing shows that acetone has no measurable effect or may in fact reduce engine life by adversely affecting fuel system parts.<ref>{{citation | url = http://www.helenair.com/articles/2006/01/21/automotive/c01012106_03.txt | publisher = Independent Record | date = 2006-01-21 | title = Click and Clack Talk Cars | first1 = Tom | first2 = Ray | last1 = Magliozzi | last2 = Magliozzi | accessdate = 2007-06-06}}.</ref><ref>{{citation | webpage-url = http://msgboard.snopes.com/message/ultimatebb.php?/ubb/get_topic/f/20/t/000594/p/1.html | webpage = Can adding Acetone to fuel increase mpg by 15 to 35%? | website = Snopes | url = Snopes.com | accessdate=2007-06-06}}.</ref>  
  
 
==Safety==
 
==Safety==
 
===Flammability===
 
===Flammability===
−
The most common hazard associated with acetone is its extreme flammability. It [[auto-ignition temperature|auto-ignites]] at a temperature of 465 °C (869 °F).  At temperatures greater than acetone's [[flash point]] of −20 °C (−4 °F), air mixtures of between 2.5% and 12.8% acetone, by volume, may explode or cause a flash fire. Vapors can flow along surfaces to distant ignition sources and flash back. Static discharge may also ignite acetone vapors.<ref>[http://www.jtbaker.com/msds/englishhtml/A0446.htm Acetone MSDS<!-- Bot generated title -->]</ref>
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The most common hazard associated with acetone is its extreme flammability. It [[auto-ignition temperature|auto-ignites]] at a temperature of 465&nbsp;°C (869&nbsp;°F).  At temperatures greater than acetone's [[flash point]] of −18&nbsp;°C (0&nbsp;°F), air mixtures of between 2.5% and 12.8% acetone, by volume, may explode or cause a flash fire. Vapors can flow along surfaces to distant ignition sources and flash back. Static discharge may also ignite acetone vapors.<ref>{{citation | url = http://www.jtbaker.com/msds/englishhtml/A0446.htm | webpage = Acetone MSDS}}.</ref>
  
 
===Acetone peroxide===
 
===Acetone peroxide===
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===Toxicology===
 
===Toxicology===
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Acetone is believed to exhibit only slight toxicity in normal use, and there is no strong evidence of chronic health effects if basic precautions are followed.<ref>http://ccohs.ca/oshanswers/chemicals/chem_profiles/acetone/basic_ace.html</ref>  
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Acetone is believed to exhibit only slight toxicity in normal use, and there is no strong evidence of chronic health effects if basic precautions are followed.<ref name="CCOHS">{{citation | url=http://ccohs.ca/oshanswers/chemicals/chem_profiles/acetone/health_ace.html | webpage = Health Effects of Acetone | accessdate = 2008-10-21 | publisher = Canadian Centre for Occupational Health and Safety}}</ref>  
  
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At very high vapor concentrations, acetone is irritating and, like many other solvents, may depress the [[central nervous system]]. It is also a severe irritant on contact with eyes, and a potential [[pulmonary aspiration]] risk. In one documented case, ingestion of a substantial amount of acetone led to systemic toxicity, although the patient eventually fully recovered.<ref>{{cite web|url=http://ccohs.ca/oshanswers/chemicals/chem_profiles/acetone/health_ace.html|title=Health Effects of Acetone|accessdate=2008-10-21|author=Canadian Centre for Occupational Health and Safety}}</ref> Some sources estimate [[median lethal dose|LD<sub>50</sub>]] for human ingestion at 1.159 g/kg; LD<sub>50</sub> inhalation by mice is given as 44 g per cubic meter, over 4 hours.<ref>[http://msds.chem.ox.ac.uk/PR/propanone.html Safety (MSDS) data for propanone<!-- Bot generated title -->]</ref>
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At very high vapor concentrations, acetone is irritating and, like many other solvents, may depress the [[central nervous system]]. It is also a severe irritant on contact with eyes, and a potential [[pulmonary aspiration]] risk. In one documented case, ingestion of a substantial amount of acetone led to systemic toxicity, although the patient eventually fully recovered.<ref name="CCOHS"/> Some sources estimate [[median lethal dose|LD<sub>50</sub>]] for human ingestion at 1.159&nbsp;g/kg; LC<sub>50</sub> inhalation by mice is given as 44&nbsp;g/m<sup>3</sup>, over 4&nbsp;hours.<ref>{{citation | url = http://msds.chem.ox.ac.uk/PR/propanone.html | webpage = Safety (MSDS) data for propanone}}.</ref>
  
−
Interestingly, acetone has been shown to have [[anticonvulsant]] effects in animal models of [[epilepsy]], in the absence of toxicity, when administered in millimolar concentrations.<ref name="Likhodii">{{cite journal|author=Likhodii SS, Serbanescu I, Cortez MA, Murphy P, Snead OC 3rd, Burnham WM|title=Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet|journal=[[Ann Neurol.]]|year=2003|volume=54|issue=2|pages=219–226|doi=10.1002/ana.10634}}</ref> It has been hypothesized that the high-fat low-carbohydrate [[ketogenic diet]] used clinically to control drug-resistant epilepsy in children works by elevating acetone in the brain.<ref name="Likhodii"/>
+
Interestingly, acetone has been shown to have [[anticonvulsant]] effects in animal models of [[epilepsy]], in the absence of toxicity, when administered in millimolar concentrations.<ref name="Likhodii">{{citation | last1 = Likhodii | first1 = S. S. | last2 = Serbanescu | first2 = I. | last3 = Cortez | first3 = M. A. | last4 = Murphy | first4 = P. |last5 = Snead | first5 = O. C., 3rd | last6 = Burnham | first6 = W. M. |title=Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet | journal = Ann. Neurol. | year = 2003 | volume = 54 | issue = 2 | pages = 219–26 | doi = 10.1002/ana.10634}}.</ref> It has been hypothesized that the high-fat low-carbohydrate [[ketogenic diet]] used clinically to control drug-resistant epilepsy in children works by elevating acetone in the brain.<ref name="Likhodii"/>
  
 
===Environmental effects===
 
===Environmental effects===
−
Acetone evaporates rapidly, even from water and soil. Once in the atmosphere, it is degraded by UV light with a 22-day half-life. Acetone dissipates slowly in soil, animals, or waterways since it is sometimes consumed by microorganisms;<ref>[http://www.atsdr.cdc.gov/tfacts21.pdf tf21<!-- Bot generated title -->]</ref> however, it is a significant issue with respect to groundwater contamination due to its high [[solubility]] in water. The [[median lethal dose|LD<sub>50</sub>]] of acetone for fish is 8.3 g/l of water (or about 0.8%) over 96 hours, and its environmental half-life is about 1 to 10 days. Acetone may pose a significant risk of oxygen depletion in aquatic systems due to the microbial activity consuming it.<ref>http://jmloveridge.com/cosh/Acetone.pdf</ref>
+
Acetone evaporates rapidly, even from water and soil. Once in the atmosphere, it is degraded by UV light with a 22-day half-life. Acetone dissipates slowly in soil, animals, or waterways since it is sometimes consumed by microorganisms;<ref>{{citation | url = http://www.atsdr.cdc.gov/tfacts21.pdf }}.</ref> however, it is a significant issue with respect to groundwater contamination due to its high [[solubility]] in water. The [[median lethal dose|LD<sub>50</sub>]] of acetone for fish is 8.3&nbsp;g/l of water (or about 0.8%) over 96&nbsp;hours, and its environmental half-life is about 1–10&nbsp;days. Acetone may pose a significant risk of oxygen depletion in aquatic systems due to the microbial activity consuming it.<ref>{{citation | url = http://jmloveridge.com/cosh/Acetone.pdf}}.</ref>
  
 
==References==
 
==References==
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==External links==
 
==External links==
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*[http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/_icsc00/icsc0087.htm International Chemical Safety Card 0087]
+
*{{ICSC|0087}}
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*[http://npi.gov.au/database/substance-info/profiles/3.html National Pollutant Inventory: Acetone]
+
*{{PGCH|0004}}
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*[http://cdc.gov/niosh/npg/npgd0004.html NIOSH Pocket Guide to Chemical Hazards]
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*{{NPI|id=3|name=Acetone}}
 +
*{{SIDS|name=Acetone|id=67641}}
 
*Calculation of [http://ddbonline.ddbst.de/AntoineCalculation/AntoineCalculationCGI.exe?component=Acetone vapor pressure], [http://ddbonline.ddbst.de/DIPPR105DensityCalculation/DIPPR105CalculationCGI.exe?component=Acetone liquid density], [http://ddbonline.ddbst.de/VogelCalculation/VogelCalculationCGI.exe?component=Acetone dynamic liquid viscosity], [http://ddbonline.ddbst.de/DIPPR106SFTCalculation/DIPPR106SFTCalculationCGI.exe?component=Acetone surface tension] of acetone
 
*Calculation of [http://ddbonline.ddbst.de/AntoineCalculation/AntoineCalculationCGI.exe?component=Acetone vapor pressure], [http://ddbonline.ddbst.de/DIPPR105DensityCalculation/DIPPR105CalculationCGI.exe?component=Acetone liquid density], [http://ddbonline.ddbst.de/VogelCalculation/VogelCalculationCGI.exe?component=Acetone dynamic liquid viscosity], [http://ddbonline.ddbst.de/DIPPR106SFTCalculation/DIPPR106SFTCalculationCGI.exe?component=Acetone surface tension] of acetone
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*[http://toxnet.nlm.nih.gov/cgi-bin/sis/search/f?./temp/~EQIVt8:1 Hazardous substances databank entry at the national library of medicine]
 
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*[http://www.fishersci.com/wps/portal/PRODUCTDETAIL?prodcutdetail='prod'&productId=677664&catalogId=29104&matchedCatNo=A18500||A18200||A181||A18S4||A184||A18P4||A18SK4||A18CU1300||A1820&pos=5&catCode=RE_SC&endecaSearchQuery=%23store%3DScientific%23N%3D0%23rpp%3D15&fromCat=yes&keepSessionSearchOutPut=true&fromSearch=Y&searchKey=acetone&highlightProductsItemsFlag=Y Fisher Chemical MSDS]
 
  
 
[[Category:Ketones]]
 
[[Category:Ketones]]

Latest revision as of 10:35, 1 September 2009

Acetone[1]
Acetone
Structure and dimensions of the acetone molecule
Ball-and-stick model of acetone
Space-filling model of acetone
IUPAC name propanone
Other names β-ketopropane, dimethyl ketone, dimethylformaldehyde, DMK, propanone, 2-propanone, propan-2-one
Identifiers
InChI InChI=1/C3H6O/c1-3(2)4/h1-2H3
InChIKey CSCPPACGZOOCGX-UHFFFAOYAF
Standard InChI InChI=1S/C3H6O/c1-3(2)4/h1-2H3
Standard InChIKey CSCPPACGZOOCGX-UHFFFAOYSA-N
CAS number [67-64-1]
EC number 200-662-2
RTECS AL31500000
ChemSpider 175
SMILES
Properties[2]
Molecular formula C3H6O
Molar mass 58.08 g mol−1
Appearance colorless liquid
Density 0.79 g/cm3
Melting point

−94.9 °C, 178 K, -139 °F

Boiling point

56.53 °C, 330 K, 134 °F

Solubility in water miscible
Vapor pressure 24 kPa (20 ºC)
Acidity (pKa) 24.2
Refractive index (nD) 1.359 (20 °C)
Viscosity 0.32 cP (20 °C)
Dipole moment 2.91 D
Structure
Molecular geometry trigonal planar at C=O
Hazards[2][3][4]
Material safety data sheet (MSDS) ICSC 0087
EU index number 606-001-00-8
GHS pictograms Flam. Liq. 2Eye Irrit. 2; STOT SE 3
GHS signal word DANGER
GHS hazard statements H225, H319, H336
Flash point -18 °C (0 ºF)
Autoignition temp. 465 °C (869 ºF)
Explosive limits 2.2–13%
PEL (U.S.) 1000 ppm TWA
LD50 >2000 mg/kg, oral (rat)
Related compounds
Other ketones Butanone
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Acetone is the organic compound with the formula OC(CH3)2. This colorless, mobile, flammable liquid is the simplest example of the ketones. Owing to the fact that acetone is miscible with water it serves as an important solvent in its own right, typically as the solvent of choice for cleaning purposes in the laboratory. More than 3 million tonnes are produced annually, mainly as a precursor to polymers.[5] Familiar household uses of acetone are as the active ingredient in nail polish remover and as paint thinner and sanitary cleaner/nail polish remover base. It is a common building block in organic chemistry. In addition to being manufactured, acetone also occurs naturally, even being biosynthesized in small amounts in the human body.

Production

Acetone is produced directly or indirectly from propene. Most commonly, in the cumene process, benzene is alkylated with propene and the resulting cumene (isopropylbenzene) is oxidized to give phenol and acetone:

C6H5CH(CH3)2 + O2 → C6H5OH + OC(CH3)2

This conversion entails the intermediacy of cumene hydroperoxide, C6H5C(OOH)(CH3)2.

Acetone is also produced by the direct oxidation of propene with a palladium(II)/copper(II) catalyst, akin to the Wacker process.

Older production methods

Previously, acetone was produced by the dry distillation of acetates, for example calcium acetate. During World War I acetone was produced via bacterial fermentation, as developed by Chaim Weizmann (later the first president of Israel) in order to help the British war effort.[5] This Acetone Butanol Ethanol process was abandoned due to the small yields.[5]

Biosynthesis

See also: ketosis

Small amounts of acetone are produced in the body by the decarboxylation of ketone bodies.

Uses

About half of the world's production of acetone is consumed as a precursor to methyl methacrylate. This application begins with the initial conversion of acetone to its cyanohydrin:

(CH3)2CO + HCN → (CH3)2C(OH)CN

In a subsequent step, the nitrile is hydrolyzed to the unsaturated amide, which is esterified:

(CH3)2C(OH)CN + CH3OH → CH2=(CH3)CCO2CH3 + NH3

The second major use of acetone entails its condensation with phenol to give bisphenol A:

(CH3)2CO + 2 C6H5OH → (CH3)2C(C6H4OH)2 + H2O

Bisphenol-A is a component of many polymers such as polycarbonates, polyurethanes, and epoxy resins.

Combustion

(CH3)2CO + 4O2 → 3CO2 + 3H2O

As a solvent

Acetone is a good solvent for most plastics and synthetic fibres including those used in Nalgene bottles made of polystyrene, polycarbonate and some types of polypropylene.[6]. It is ideal for thinning fiberglass resin, cleaning fiberglass tools and dissolving two-part epoxies and superglue before hardening. It is used as a volatile component of some paints and varnishes. As a heavy-duty degreaser, it is useful in the preparation of metal prior to painting; it also thins polyester resins, vinyl and adhesives.

Many millions of kilograms of acetone are consumed in the production of the solvents methyl isobutyl alcohol and methyl isobutyl ketone. These products arise via an initial aldol condensation to give diacetone alcohol.[5]

2(CH3)2CO → (CH3)2C(OH)CH2C(O)CH3

Acetone is used as a solvent by the pharmaceutical industry and as a denaturation agent in denatured alcohol.[7] Acetone is also present as an excipient in some pharmaceutical products.[8]

Storage of acetylene

Although flammable itself, acetone is also used extensively as a solvent for the safe transporting and storing of acetylene, which cannot be safely pressurized as a pure compound. Vessels containing a porous material are first filled with acetone followed by acetylene, which dissolves into the acetone. One liter of acetone can dissolve around 250 liters of acetylene.[9][10]

Laboratory uses

In the laboratory, acetone is used as a polar aprotic solvent in a variety of organic reactions, such as SN2 reactions. The use of acetone solvent is also critical for the Jones oxidation. It is a common solvent for rinsing laboratory glassware because of its low cost, volatility, and ability to dissolve water. For similar reasons, acetone is also used as a drying agent. Acetone can be cooled with dry ice to -78 °C without freezing; acetone/dry ice baths are commonly used to conduct reactions at low temperatures. Acetone is fluorescent under ultraviolet light, and acetone vapor may be used as a fluorescent tracer in fluid flow experiments.[11]

Domestic and other niche uses

Acetone is often the primary component in cleaning agents such as nail polish remover. Ethyl acetate, another organic solvent, is sometimes used as well. Acetone is a component of superglue remover and it easily removes residues from glass and porcelain.

It can be used as an artistic agent; when rubbed on the back of a laser print or photocopy placed face-down on another surface and burnished firmly, the toner of the image is allowed to transfer to the destination surface.

Some automotive enthusiasts add acetone at around 1 part in 500 to their fuel, following claims of dramatic improvement in fuel economy and engine life.[12] This practice is controversial as the body of systematic testing shows that acetone has no measurable effect or may in fact reduce engine life by adversely affecting fuel system parts.[13][14]

Safety

Flammability

The most common hazard associated with acetone is its extreme flammability. It auto-ignites at a temperature of 465 °C (869 °F). At temperatures greater than acetone's flash point of −18 °C (0 °F), air mixtures of between 2.5% and 12.8% acetone, by volume, may explode or cause a flash fire. Vapors can flow along surfaces to distant ignition sources and flash back. Static discharge may also ignite acetone vapors.[15]

Acetone peroxide

Main article: acetone peroxide

When oxidized, acetone forms acetone peroxide as a byproduct, which is a highly unstable compound. It may be formed accidentally, e.g. when waste hydrogen peroxide is poured into waste solvent containing acetone. Acetone peroxide is more than ten times as friction and shock sensitive as nitroglycerin. Due to its instability, it is rarely used, despite its easy chemical synthesis.

Toxicology

Acetone is believed to exhibit only slight toxicity in normal use, and there is no strong evidence of chronic health effects if basic precautions are followed.[16]

At very high vapor concentrations, acetone is irritating and, like many other solvents, may depress the central nervous system. It is also a severe irritant on contact with eyes, and a potential pulmonary aspiration risk. In one documented case, ingestion of a substantial amount of acetone led to systemic toxicity, although the patient eventually fully recovered.[16] Some sources estimate LD50 for human ingestion at 1.159 g/kg; LC50 inhalation by mice is given as 44 g/m3, over 4 hours.[17]

Interestingly, acetone has been shown to have anticonvulsant effects in animal models of epilepsy, in the absence of toxicity, when administered in millimolar concentrations.[18] It has been hypothesized that the high-fat low-carbohydrate ketogenic diet used clinically to control drug-resistant epilepsy in children works by elevating acetone in the brain.[18]

Environmental effects

Acetone evaporates rapidly, even from water and soil. Once in the atmosphere, it is degraded by UV light with a 22-day half-life. Acetone dissipates slowly in soil, animals, or waterways since it is sometimes consumed by microorganisms;[19] however, it is a significant issue with respect to groundwater contamination due to its high solubility in water. The LD50 of acetone for fish is 8.3 g/l of water (or about 0.8%) over 96 hours, and its environmental half-life is about 1–10 days. Acetone may pose a significant risk of oxygen depletion in aquatic systems due to the microbial activity consuming it.[20]

References

  1. ↑ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals, 11th ed.; Merck, 1989. ISBN 091191028X, 58.
  2. ↑ 2.0 2.1 Acetone; International Chemical Safety Card 0087; International Labour Organization: Geneva, April 1994, <http://www.inchem.org/documents/icsc/icsc/eics0087.htm>.
  3. ↑ Index no. 606-001-00-8 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at p 517.
  4. ↑ Acetone. In Pocket Guide to Chemical Hazards; U.S. Department of Health and Human Services (NIOSH) Publication No. 2005-149; Government Printing Office: Washington, DC, 2005. ISBN 9780160727511, <http://www.cdc.gov/niosh/npg/default.html>.
  5. ↑ 5.0 5.1 5.2 5.3 Sifniades, Stylianos; Levy, Alan B. Acetone. In Ullmann’s Encyclopedia of Industrial Chemistry, 5th ed.; Wiley-VCH: Weinheim, 2005.
  6. ↑ NALGENE Labware - Technical Data
  7. ↑ Weiner, Myra L.; Kotkoskie, Lois A. Excipient Toxicity and Safety, 1999; p 32. ISBN 0824782100
  8. ↑ , <http://www.accessdata.fda.gov/scripts/cder/iig/index.cfm>.
  9. ↑ Safety Hazard Information - Special Hazards of Acetylene, <http://www.msha.gov/alerts/hazardsofacetylene.htm>, U.S. Mine Safety and Health Administration (MSHA).
  10. ↑ History - Acetylene dissolved in acetone, <http://www.aga.com/web/web2000/com/WPPcom.nsf/pages/History_Acetylene_1>.
  11. ↑ Lozano, A.; Yip, B.; Hanson, R. K. Acetone: a tracer for concentration measurements in gaseous flows by planar laser-induced fluorescence. Exp. Fluids 1992, 13, 369–76. DOI: 10.1007/BF00223244.
  12. ↑ LaPonte, Louis Acetone in Fuels (A Study of Dimethylketone or Propanone), <http://www.brightgreen.us/lubedev/smartgas/additive.htm> (accessed 6 June 2007), Smartgas.net; .
  13. ↑ Magliozzi, Tom; Magliozzi, Ray Click and Clack Talk Cars; Independent Record, 2006-01-21, <http://www.helenair.com/articles/2006/01/21/automotive/c01012106_03.txt>. (accessed 6 June 2007).
  14. ↑ Can adding Acetone to fuel increase mpg by 15 to 35%?, <http://msgboard.snopes.com/message/ultimatebb.php?/ubb/get_topic/f/20/t/000594/p/1.html> (accessed 6 June 2007), Snopes; .
  15. ↑ Acetone MSDS, <http://www.jtbaker.com/msds/englishhtml/A0446.htm>.
  16. ↑ 16.0 16.1 Health Effects of Acetone, <http://ccohs.ca/oshanswers/chemicals/chem_profiles/acetone/health_ace.html> (accessed 21 October 2008), Canadian Centre for Occupational Health and Safety
  17. ↑ Safety (MSDS) data for propanone, <http://msds.chem.ox.ac.uk/PR/propanone.html>.
  18. ↑ 18.0 18.1 Likhodii, S. S.; Serbanescu, I.; Cortez, M. A.; Murphy, P.; Snead, O. C., 3rd; Burnham, W. M. Anticonvulsant properties of acetone, a brain ketone elevated by the ketogenic diet. Ann. Neurol. 2003, 54 (2), 219–26. DOI: 10.1002/ana.10634.
  19. ↑ , <http://www.atsdr.cdc.gov/tfacts21.pdf>.
  20. ↑ , <http://jmloveridge.com/cosh/Acetone.pdf>.

External links

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