Difference between revisions of "Aluminium chloride"

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| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
 
|  Reference = <ref>{{CLP Regulation|index=013-003-00-7|page=366}}</ref>
 
|  Reference = <ref>{{CLP Regulation|index=013-003-00-7|page=366}}</ref>
|  ExternalMSDS = {{ICSC-small|11|25}}
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|  ExternalMSDS = {{ICSC-small|1125}}
 
|  EUIndex = 013-003-00-7
 
|  EUIndex = 013-003-00-7
 
|  GHSPictograms = {{GHS05|Skin Corr. 1B}}
 
|  GHSPictograms = {{GHS05|Skin Corr. 1B}}
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|  CASNo = 7784-13-6 <!-- verified with ChemSpider and the NZ HSNO Chemical Classification Information Database -->
 
|  CASNo = 7784-13-6 <!-- verified with ChemSpider and the NZ HSNO Chemical Classification Information Database -->
 
|  EC-number = 231-208-1
 
|  EC-number = 231-208-1
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|  ATCCode_prefix = D10
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|  ATCCode_suffix = AX01
 
|  ChemSpiderID = 22970
 
|  ChemSpiderID = 22970
 
|  PubChem = 24012
 
|  PubChem = 24012
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   }}
 
   }}
 
| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
|  Reference = <ref>{{GHS class NZ|id=12437|accessdate=2009-08-22}}.</ref>
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|  Reference = <ref>{{GHS class NZ|id=8011|accessdate=2009-08-22}}.</ref>
 
|  GHSPictograms = {{GHS corrosion|Corr. Met. 1, Skin Corr. 1C, Eye Dam. 1}}{{GHS exclamation mark|Acute Tox. (oral) 4}}
 
|  GHSPictograms = {{GHS corrosion|Corr. Met. 1, Skin Corr. 1C, Eye Dam. 1}}{{GHS exclamation mark|Acute Tox. (oral) 4}}
 
|  GHSSignalWord = DANGER
 
|  GHSSignalWord = DANGER
 
|  HPhrases = {{H-phrases|280|290|302|314}}
 
|  HPhrases = {{H-phrases|280|290|302|314}}
|  PPhrases = {{P-phrases|234|260|264|270|280|301+312|301+330+331|303+361+353|304+340|305+351+338 |310|321|363|390|405|406|501}}
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|  PPhrases = {{P-phrases|234|260|264|270|280|301+312|301+330+331|303+361+353|304+340|305+351+338 |310|321|363|405|406|501}}
 
|  FlashPt = non-flammable
 
|  FlashPt = non-flammable
 
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*{{PGCH|0024}}
 
*{{PGCH|0024}}
 
*{{EHC|194|name=Aluminium}}
 
*{{EHC|194|name=Aluminium}}
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*{{HSDB|name=Aluminum chloride}}
 
*{{OrgSynth preps|id=33169|name=aluminium chloride}}
 
*{{OrgSynth preps|id=33169|name=aluminium chloride}}
 
* [http://loradchemical.com/aluminum-chloride-2.html Aluminum chloride Information]
 
* [http://loradchemical.com/aluminum-chloride-2.html Aluminum chloride Information]
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[[Category:Metal halides]]
 
[[Category:Metal halides]]
 
[[Category:Reagents for organic chemistry]]
 
[[Category:Reagents for organic chemistry]]
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[[Category:Anti-acne preparations]]
  
 
{{Imported from Wikipedia|name=Aluminium chloride|id=300971436}}
 
{{Imported from Wikipedia|name=Aluminium chloride|id=300971436}}

Latest revision as of 07:02, 13 December 2009

Aluminium trichloride (anhydrous)
Aluminium trichloride dimer
IUPAC name aluminium trichloride
trichloroalumane
trichloridoaluminium
Other names aluminum trichloride
Identifiers
InChI InChI=1/Al.3ClH/h;3*1H/q+3;;;/p-3
InChIKey VSCWAEJMTAWNJL-DFZHHIFOAR
Standard InChI InChI=1S/Al.3ClH/h;3*1H/q+3;;;/p-3
Standard InChIKey VSCWAEJMTAWNJL-UHFFFAOYSA-K
CAS number [7446-70-0]
EC number 231-208-1
RTECS BD0530000
ChemSpider 22445
PubChem 24012
Properties[1]
Chemical formula AlCl3
Molar mass 133.34 g/mol (anhydrous)
Appearance white or pale yellow solid, very hygroscopic
Density 2.44 g/cm3 (25 ºC), solid
1.31 g/cm3 (200 ºC), liquid
Melting point

190 °C at 2.5 atm

Boiling point

177.8 °C subl.

Solubility in water reacts violently
Solubility in ethanol 100 g/100 ml
Solubility in chloroform 0.072 g/100 ml
Solubility in benzene slightly soluble
Solubility soluble in carbon tetrachloride, diethyl ether
Structure
Crystal structure Monoclinic, mS16
Space group C12/m1, No. 12
Coordination geometry Octahedral (Al3+)
Hazards[2]
Material safety data sheet (MSDS) ICSC 1125
EU index number 013-003-00-7
GHS pictograms Skin Corr. 1B
GHS signal word DANGER
GHS hazard statements H314
Related compounds
Other anions Aluminium fluoride
Aluminium bromide
Aluminium iodide
Other cations Boron trichloride
Gallium(III) chloride
Indium(III) chloride
Thallium(III) chloride
Other Lewis acids Iron(III) chloride
Boron trifluoride
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Aluminium trichloride hexahydrate
Aluminium trichloride hexahydrate
IUPAC name aluminium trichloride—water (1/6)
Identifiers
InChI InChI=1/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
InChIKey JGDITNMASUZKPW-DFZHHIFOAF
Standard InChI InChI=1S/Al.3ClH.6H2O/h;3*1H;6*1H2/q+3;;;;;;;;;/p-3
Standard InChIKey JGDITNMASUZKPW-UHFFFAOYSA-K
CAS number [7784-13-6]
EC number 231-208-1
RTECS BD0530000
ATC code D10AX01
ChemSpider 22970
PubChem 24012
Properties[1]
Chemical formula AlCl3·6H2O
Molar mass 241.43 g/mol
Appearance colourless or white solid, hygroscopic
Density 2.398 g/cm3
Melting point

100 °C decomp.

Solubility in water 45.8 g/100 ml (20 °C)
48.6 g/100 ml (80 °C)
Solubility in ethanol 50 g/100 ml
Solubility in diethyl ether soluble
Solubility in hydrochloric acid slightly soluble
Refractive index (nD) 1.6
Hazards[3]
GHS pictograms Corr. Met. 1, Skin Corr. 1C, Eye Dam. 1Acute Tox. (oral) 4
GHS signal word DANGER
GHS hazard statements H280, H290, H302, H314
GHS precautionary statements P234, P260, P264, P270, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405
Flash point non-flammable
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Aluminium chloride (AlCl3) is a compound of aluminium and chlorine. The solid has a low melting and boiling point, and is covalently bonded. It sublimes at 178 °C. Molten AlCl3 conducts electricity poorly,[4] unlike more ionic halides such as sodium chloride.

AlCl3 adopts the YCl3 structure in the solid, featuring a cubic close packed array of chloride ions with Al3+ ions occupying one-third of the octahedral holes, forming a layered structure.[5] Upon melting AlCl3 gives the dimer Al2Cl6, which can vaporise. At higher temperatures this Al2Cl6 dimer dissociates into trigonal planar AlCl3, which is structurally analogous to BF3.

The three structures of aluminium trichloride

Aluminium chloride is highly deliquescent, and can explode upon abrupt contact with water because of the high heat of hydration. Aqueous solutions of AlCl3 are ionic and thus conduct electricity well. Such solutions are found to be acidic, indicative of partial hydrolysis of the Al3+ ion. The reactions can be described (simplified) as:

[Al(H2O)6]3+ + H2O [Al(OH)(H2O)5]2+ + H3O+

AlCl3 is probably the most commonly used Lewis acid and also one of the most powerful. It finds widespread application in the chemical industry as the classic catalyst for Friedel–Crafts reactions, both acylations and alkylations. It also finds use in polymerization and isomerization reactions of hydrocarbons. Aluminium also forms a lower chloride, aluminium(I) chloride (AlCl), but this is very unstable and only known in the vapor phase.[4]

Chemical properties

Aluminium chloride is a powerful Lewis acid, capable of forming stable Lewis acid-base adducts with even weak Lewis bases such as benzophenone or mesitylene.[6] Not surprisingly it forms AlCl4 in the presence of chloride ions.

In water, partial hydrolysis forms hydrogen chloride or H3O+, as described in the overview above. Aqueous solutions behave similarly to other aluminium salts containing hydrated Al3+ ions, giving a gelatinous precipitate of aluminium hydroxide upon reaction with the correct quantity of aqueous sodium hydroxide:

AlCl3 + 3NaOH → Al(OH)3 + 3NaCl

Preparation

Aluminium chloride is manufactured on a large scale by the exothermic reaction of aluminium metal with chlorine or hydrogen chloride at 650–750 °C.[4]

2Al + 3Cl2 → 2AlCl3
2Al + 6HCl → 2AlCl3 + 3H2

Hydrated forms are prepared by dissolving aluminium oxides with dry hydrochloric acid at 150 °C.

Uses

The Friedel–Crafts reaction is the major use for aluminium chloride, for example in the preparation of anthraquinone (for the dyestuffs industry) from benzene and phosgene.[4][6] In the general Friedel–Crafts reaction, an acyl chloride or alkyl halide reacts with an aromatic system as shown:[6]

AlCl3 FriedelCrafts.gif

With benzene derivatives, the major product is the para-isomer. The alkylation reaction has many associated problems, so it is less widely used than the acylation reaction. For both reactions, the aluminium chloride, as well as other materials and the equipment, must be moderately dry, although a trace of moisture is necessary for the reaction to proceed. A general problem with the Friedel–Crafts reaction is that the aluminium chloride "catalyst" needs to be present in full stoichiometric quantities in order for the reaction to go to completion, because it complexes strongly with the products (see chemical properties above). This makes it very difficult to recycle, so it must be destroyed after use, generating a large amount of corrosive waste. For this reason chemists are examining the use of more environmentally benign catalysts such as ytterbium(III) triflate or dysprosium(III) triflate, which can be recycled.

Aluminium chloride can also be used to introduce aldehyde groups onto aromatic rings, for example via the Gattermann–Koch reaction, which uses carbon monoxide, hydrogen chloride and a copper(I) chloride co-catalyst:[7]

AlCl3 formylation.gif

Aluminium chloride finds a wide variety of other applications in organic chemistry.[8] For example, it can catalyse the "ene reaction", such as the addition of 3-buten-2-one (methyl vinyl ketone) to carvone:[9]

AlCl3 ene rxn.gif

AlCl3 is also widely used for polymerization and isomerization reactions of hydrocarbons. Important examples include the manufacture of ethylbenzene, which used to make styrene and thus polystyrene, and also production of dodecylbenzene, which is used for making detergents.[4]

Aluminium chloride combined with aluminium in the presence of an arene can be used to synthesize bis(arene) metal complexes, e.g. bis(benzene)chromium, from certain metal halides via the so-called Fischer–Hafner synthesis.

Aluminium chloride, often in the form of derivatives such as aluminium chlorohydrate, is a common component in antiperspirants at low concentrations. Hyperhidrosis sufferers need a much higher concentration (15% or higher), sold under such brand names as Drysol, Maxim, Odaban, CertainDri, B+Drier, Anhydrol Forte and Driclor.

Chemical reactions

Aluminium chloride reacts with calcium and magnesium hydrides in tetrahydrofuran forming tetrahydroaluminates:

AlCl3 + 3LiH → AlH3 + 3LiCl

The hexahydrate decomposes to aluminum oxide when heated at 300 °C:[10]

2AlCl3·6H2O → Al2O3 + 6HCl + 3H2O

Precautions

Anhydrous AlCl3 reacts vigorously with water and bases, so suitable precautions are required. Hydrated salts are less problematic.

References

  1. 1.0 1.1 CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-73. ISBN 0-8493-0462-8.
  2. Index no. 013-003-00-7 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 366.
  3. HSNO Chemical Classification Information Database, <http://www.ermanz.govt.nz/Chemicals/ChemicalDisplay.aspx?SubstanceID=8011> (accessed 22 August 2009), New Zealand Environmental Risk Management Authority.
  4. 4.0 4.1 4.2 4.3 4.4 Greenwood, Norman N.; Earnshaw, A. Chemistry of the Elements; Pergamon: Oxford, 1984; pp 262–66. ISBN 0-08-022057-6.
  5. Wells, A. F. Structural Inorganic Chemistry, 5th ed.; Clarendon Press: Oxford, 1984. ISBN 0-19-855370-6.
  6. 6.0 6.1 6.2 Friedel-Crafts and Related Reactions; Olah, G. A., Ed.; Wiley–Interscience: New York, 1963; Vol. 1.
  7. Wade, L. G. Organic Chemistry, 5th ed.; Prentice Hall: New York, 2003.
  8. Galatsis, P. In Handbook of Reagents for Organic Synthesis: Acidic and Basic Reagents; Reich, Hans J.; Rigby, James H., Eds.; Wiley: New York, 1999; pp 12–15. ISBN 0471979252.
  9. Snider, B. B. Lewis-acid catalyzed ene reactions. Acc. Chem. Res. 1980, 13 (11), 426–32. DOI: 10.1021/ar50155a007.
  10. Patnaik, Pradyot Handbook of Inorganic Chemicals; McGraw-Hill: New York, 2002. ISBN 0070494398.

External links

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