Difference between revisions of "Dioxane"

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| Name = 1,4-Dioxane
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| Reference =
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| IUPACName = 1,4-Dioxane<br>1,4-Dioxacyclohexane
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| PIN =
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| SystematicName =
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| OtherNames = [1,4]Dioxane<br>[6]-crown-2<br>p-Dioxane<br>Diethylene dioxide<br>Diethylene ether<br>Dioxan
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| ImageFile = Dioxane from antifreeze by NurdRage.jpg
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| ImageSize = 300
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| ImageCaption = 1,4-Dioxane prepared from [[ethylene glycol]] antifreeze
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| Section1 = {{Chembox Identifiers
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| 3DMet =
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| Section2 = {{Chembox Properties
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| AtmosphericOHRateConstant =
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| Appearance = Colorless liquid
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| BoilingPt =
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| BoilingPtC = 101.1
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| BoilingPt_ref =
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| BoilingPt_notes =
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| Density = 1.033 g/mL
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| Formula = C<sub>4</sub>H<sub>8</sub>O<sub>2</sub>
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| HenryConstant =
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| LogP =
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| MolarMass = 88.11 g/mol
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| MeltingPt =
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| MeltingPtC = 11.8
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| Odor = Ether-like
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| pKa =
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| pKb =
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| Solubility = Miscible
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| SolubleOther = Miscible with most organic solvents
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| VaporPressure = 29 mmHg (20 °C)
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| DeltaGf =
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| DeltaHc = -2,363 kJ/mol
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| DeltaHf = -354 kJ/mol
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| Entropy = 196.6 J·K<sup>−1</sup>·mol<sup>−1</sup>
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| HeatCapacity =
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| Section6 = {{Chembox Hazards
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| AutoignitionPt =
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| ExploLimits = 2.0%-22%
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| ExternalMSDS = [https://www.docdroid.net/1HBVEMG/14-dioxane-sa.pdf.html Sigma-Aldrich]
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| FlashPt = 12 °C (54 °F; 285 K)
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| LD50 = 5.7 g/kg (mouse, oral)<br>5.2 g/kg (rat, oral)<br>3.9 g/kg (guinea pig, oral)<br>7.6 g/kg (rabbit, dermal)
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| LC50 = 10,109 ppm (mouse, 2 hr)<br>12,568 ppm (rat, 2 hr)
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| MainHazards = Flammable<br>Carcinogen
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| Section7 = {{Chembox Related
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| OtherAnions =
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| OtherCompounds = [[Dimethyl dioxane]]<br>[[Ethylene oxide]]<br>[[Tetrahydrofuran]]
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'''1,4-Dioxane''', also known as '''diethylene ether''', '''diethylene dioxide''' or simply '''dioxane''', as the 1,2 and 1,3 isomers are rarely encountered, is a heterocyclic organic compound, a cyclic ether.
 
'''1,4-Dioxane''', also known as '''diethylene ether''', '''diethylene dioxide''' or simply '''dioxane''', as the 1,2 and 1,3 isomers are rarely encountered, is a heterocyclic organic compound, a cyclic ether.
  
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===Chemical===
 
===Chemical===
 
Dioxane can be reacted with dry chlorine gas to yield trans-2,3-dichloro-1,4-dioxane.
 
Dioxane can be reacted with dry chlorine gas to yield trans-2,3-dichloro-1,4-dioxane.
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Dioxane burns with a smokeless yellow-white flame.
  
 
===Physical===
 
===Physical===
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==Preparation==
 
==Preparation==
Dioxane is produced by the acid-catalysed dehydration of [[ethylene glycol]].
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Dioxane is produced by the acid-catalysed dehydration of [[ethylene glycol]], using conc. [[sulfuric acid]] as catalyst. The reaction takes place under reflux. Commercial anti-freeze can be safely used as EG source, regardless of impurities and additives, though concentrated anti-freeze gives a better yield than the diluted version.
  
 
Frogfot wrote a [http://web.archive.org/web/20071011001804/www.frogfot.com/synthesis/dioxane.html synthesis of dioxane].
 
Frogfot wrote a [http://web.archive.org/web/20071011001804/www.frogfot.com/synthesis/dioxane.html synthesis of dioxane].
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*Stabilize trichloroethane
 
*Stabilize trichloroethane
 
*Medium for organic reactions
 
*Medium for organic reactions
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*Purification of metallic [[sodium]] from sodium-magnesium oxide aggregate
  
 
==Handling==
 
==Handling==
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Dioxane is considered carcinogenic. It is also very flammable.
 
Dioxane is considered carcinogenic. It is also very flammable.
  
Dioxane is sometimes confused with dioxin.
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Dioxane is sometimes confused with dioxin, though the two compounds are very different.
  
 
===Storage===
 
===Storage===
Dioxane should be stored in closed bottles, with a reducing agent to prevent the formation of peroxides.
+
Dioxane should be stored in closed bottles, with a reducing agent to prevent the formation of peroxides. Dioxane is safe to keep without anti-oxidants for maximum one year, after which the levels of peroxides become too dangerous to handle.
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Since dioxane has a relative high melting point, of 11.8 °C, it's possible to store the dioxane in a fridge or freezer, where it will stay solid, thus limiting its volatility and most importantly block the formation of peroxides.  
  
 
===Disposal===
 
===Disposal===
Dioxane can be safely burned, if there are no peroxides. If the dioxane tests positive for peroxides, neutralize peroxides first. Reducing agents, like as ferrous sulfate, sodium bisulfite or metabisulfite added in excess can be used to neutralize the peroxides. After incineration, the ether should be tested again for peroxides and if none are present, it can be safely burned. If it's an old bottle, which has peroxides on the cap, do not open the bottle, instead take it to a remote of special area and safely detonate it. The latter may or require professional help.
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Dioxane can be safely burned, as long as it contains no detectable amounts of peroxides. If the dioxane tests positive for peroxides, but there is no visible precipitate in the ether, it's possible to neutralize the dissolved peroxides. Reducing agents, like [[Iron(II) sulfate|ferrous sulfate]], [[sodium bisulfite]] or [[sodium metabisulfite|metabisulfite]] added in excess can be used to neutralize the peroxides. After neutralization, the ether should be tested again for peroxides and if none are present, it can be safely burned.
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If it's an old bottle, which has visible peroxide in the solution, or if very old, is very likely to have peroxides on the cap, DO NOT OPEN THE BOTTLE! Instead take it to a remote of special area and safely detonate it. The latter may or may not require professional help, depending on the severity of the case.
  
 
==References==
 
==References==
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[[Category:Nonpolar solvents]]
 
[[Category:Nonpolar solvents]]
 
[[Category:Liquids]]
 
[[Category:Liquids]]
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[[Category:Air-sensitive materials]]
 
[[Category:Peroxide forming chemicals]]
 
[[Category:Peroxide forming chemicals]]

Revision as of 09:44, 5 January 2019

1,4-Dioxane
Dioxane from antifreeze by NurdRage.jpg
1,4-Dioxane prepared from ethylene glycol antifreeze
Names
IUPAC names
1,4-Dioxane
1,4-Dioxacyclohexane
Other names
[1,4]Dioxane
[6]-crown-2
p-Dioxane
Diethylene dioxide
Diethylene ether
Dioxan
Properties
C4H8O2
Molar mass 88.11 g/mol
Appearance Colorless liquid
Odor Ether-like
Density 1.033 g/mL
Melting point 11.8 °C (53.2 °F; 284.9 K)
Boiling point 101.1 °C (214.0 °F; 374.2 K)
Miscible
Solubility Miscible with most organic solvents
Vapor pressure 29 mmHg (20 °C)
Thermochemistry
196.6 J·K−1·mol−1
-354 kJ/mol
Hazards
Safety data sheet Sigma-Aldrich
Flash point 12 °C (54 °F; 285 K)
Lethal dose or concentration (LD, LC):
5.7 g/kg (mouse, oral)
5.2 g/kg (rat, oral)
3.9 g/kg (guinea pig, oral)
7.6 g/kg (rabbit, dermal)
10,109 ppm (mouse, 2 hr)
12,568 ppm (rat, 2 hr)
Related compounds
Related compounds
Dimethyl dioxane
Ethylene oxide
Tetrahydrofuran
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

1,4-Dioxane, also known as diethylene ether, diethylene dioxide or simply dioxane, as the 1,2 and 1,3 isomers are rarely encountered, is a heterocyclic organic compound, a cyclic ether.

Properties

Chemical

Dioxane can be reacted with dry chlorine gas to yield trans-2,3-dichloro-1,4-dioxane.

Dioxane burns with a smokeless yellow-white flame.

Physical

Dioxane is a colorless liquid, with a faint sweet odor similar to that of diethyl ether. It is miscible with many solvents and is hygroscopic. Dioxane boils at 101.1 °C and freezes at 11.8 °C.

Availability

Dioxan can be bought from eBay.

Preparation

Dioxane is produced by the acid-catalysed dehydration of ethylene glycol, using conc. sulfuric acid as catalyst. The reaction takes place under reflux. Commercial anti-freeze can be safely used as EG source, regardless of impurities and additives, though concentrated anti-freeze gives a better yield than the diluted version.

Frogfot wrote a synthesis of dioxane.

Projects

  • Stabilize trichloroethane
  • Medium for organic reactions
  • Purification of metallic sodium from sodium-magnesium oxide aggregate

Handling

Safety

Dioxane is considered carcinogenic. It is also very flammable.

Dioxane is sometimes confused with dioxin, though the two compounds are very different.

Storage

Dioxane should be stored in closed bottles, with a reducing agent to prevent the formation of peroxides. Dioxane is safe to keep without anti-oxidants for maximum one year, after which the levels of peroxides become too dangerous to handle.

Since dioxane has a relative high melting point, of 11.8 °C, it's possible to store the dioxane in a fridge or freezer, where it will stay solid, thus limiting its volatility and most importantly block the formation of peroxides.

Disposal

Dioxane can be safely burned, as long as it contains no detectable amounts of peroxides. If the dioxane tests positive for peroxides, but there is no visible precipitate in the ether, it's possible to neutralize the dissolved peroxides. Reducing agents, like ferrous sulfate, sodium bisulfite or metabisulfite added in excess can be used to neutralize the peroxides. After neutralization, the ether should be tested again for peroxides and if none are present, it can be safely burned.

If it's an old bottle, which has visible peroxide in the solution, or if very old, is very likely to have peroxides on the cap, DO NOT OPEN THE BOTTLE! Instead take it to a remote of special area and safely detonate it. The latter may or may not require professional help, depending on the severity of the case.

References

Relevant Sciencemadness threads