Misplaced Pages

Aluminium chloride

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is the current revision of this page, as edited by Sphilbrick (talk | contribs) at 19:23, 5 December 2024 (Reverted good faith edits by GothicWindow452 (talk)). The present address (URL) is a permanent link to this version.

Revision as of 19:23, 5 December 2024 by Sphilbrick (talk | contribs) (Reverted good faith edits by GothicWindow452 (talk))(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff) Chemical compound

Aluminium chloride
Aluminium(III) chloride
Aluminium trichloride hexahydrate, pure (top), and contaminated with iron(III) chloride (bottom)
Aluminium trichloride dimer
Aluminium trichloride dimer
Aluminium trichloride unit cell
Aluminium trichloride unit cell
Names
IUPAC name Aluminium chloride
Other names Aluminium(III) chloride
Aluminium trichloride
Trichloroaluminum
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.028.371 Edit this at Wikidata
EC Number
  • 231-208-1
Gmelin Reference 1876
PubChem CID
RTECS number
  • BD0530000
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/Al.3ClH/h;3*1H/q+3;;;/p-3Key: VSCWAEJMTAWNJL-UHFFFAOYSA-K
  • InChI=1/Al.3ClH/h;3*1H/q+3;;;/p-3Key: VSCWAEJMTAWNJL-DFZHHIFOAR
SMILES
  • monomer: Cl(Cl)Cl
  • dimer: Cl1(Cl)(1)(Cl)Cl
  • hexahydrate: ()()()()...
Properties
Chemical formula AlCl3
Molar mass
  • 133.341 g/mol (anhydrous)
  • 241.432 g/mol (hexahydrate)
Appearance Colourless crystals, hygroscopic
Density
  • 2.48 g/cm (anhydrous)
  • 2.398 g/cm (hexahydrate)
Melting point
  • 180 °C (356 °F; 453 K) (anhydrous, sublimes)
  • 100 °C (212 °F; 373 K) (hexahydrate, decomposes)
Solubility in water
  • 439 g/L (0 °C)
  • 449 g/L (10 °C)
  • 458 g/L (20 °C)
  • 466 g/L (30 °C)
  • 473 g/L (40 °C)
  • 481 g/L (60 °C)
  • 486 g/L (80 °C)
  • 490 g/L (100 °C)
Solubility
  • Soluble in hydrogen chloride, ethanol, chloroform, carbon tetrachloride
  • Slightly soluble in benzene
Vapor pressure
  • 133.3 Pa (99 °C)
  • 13.3 kPa (151 °C)
Viscosity
  • 0.35 cP (197 °C)
  • 0.26 cP (237 °C)
Structure
Crystal structure Monoclinic, mS16
Space group C12/m1, No. 12
Lattice constant a = 0.591 nm, b = 0.591 nm, c = 1.752 nm
Lattice volume (V) 0.52996 nm
Formula units (Z) 6
Coordination geometry Octahedral (solid)
Tetrahedral (liquid)
Molecular shape Trigonal planar
(monomeric vapour)
Thermochemistry
Heat capacity (C) 91.1 J/(mol·K)
Std molar
entropy
(S298)
109.3 J/(mol·K)
Std enthalpy of
formation
fH298)
−704.2 kJ/mol
Gibbs free energyfG) −628.8 kJ/mol
Pharmacology
ATC code D10AX01 (WHO)
Hazards
GHS labelling:
Pictograms GHS05: Corrosive
Signal word Danger
Hazard statements H314
Precautionary statements P260, P280, P301+P330+P331, P303+P361+P353, P305+P351+P338+P310, P310
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
3 0 2
Lethal dose or concentration (LD, LC):
LD50 (median dose) 380 mg/kg, rat (oral, anhydrous)
3311 mg/kg, rat (oral, hexahydrate)
NIOSH (US health exposure limits):
PEL (Permissible) None
REL (Recommended) 2 mg/m
IDLH (Immediate danger) N.D.
Related compounds
Other anions
Other cations
Related Lewis acids
Supplementary data page
Aluminium chloride (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound Pharmaceutical compound
Aluminium chloride
Clinical data
AHFS/Drugs.comMonograph
License data
Routes of
administration
Topical
ATC code
  • None
Identifiers
CompTox Dashboard (EPA)
ECHA InfoCard100.028.371 Edit this at Wikidata
Data page
Aluminium chloride (data page)

Aluminium chloride, also known as aluminium trichloride, is an inorganic compound with the formula AlCl3. It forms a hexahydrate with the formula [Al(H2O)6]Cl3, containing six water molecules of hydration. Both the anhydrous form and the hexahydrate are colourless crystals, but samples are often contaminated with iron(III) chloride, giving them a yellow colour.

The anhydrous form is commercially important. It has a low melting and boiling point. It is mainly produced and consumed in the production of aluminium, but large amounts are also used in other areas of the chemical industry. The compound is often cited as a Lewis acid. It is an example of an inorganic compound that reversibly changes from a polymer to a monomer at mild temperature.

History

The salt was known in the 18th century as muriate of alumina, marine alum, argillaceous marine salt, muriated clay. It was first chemically studied in the 1830s.

This section needs expansion. You can help by adding to it. (November 2024)

Structure

Illustration of structures of aluminium chloride

Anhydrous

AlCl3 adopts three structures, depending on the temperature and the state (solid, liquid, gas). Solid AlCl3 has a sheet-like layered structure with cubic close-packed chloride ions. In this framework, the Al centres exhibit octahedral coordination geometry. Yttrium(III) chloride adopts the same structure, as do a range of other compounds. When aluminium trichloride is in its melted state, it exists as the dimer Al2Cl6, with tetracoordinate aluminium. This change in structure is related to the lower density of the liquid phase (1.78 g/cm) versus solid aluminium trichloride (2.48 g/cm). Al2Cl6 dimers are also found in the vapour phase. At higher temperatures, the Al2Cl6 dimers dissociate into trigonal planar AlCl3 monomer, which is structurally analogous to BF3. The melt conducts electricity poorly, unlike more ionic halides such as sodium chloride.

Aluminium chloride monomer belongs to the point group D3h in its monomeric form and D2h in its dimeric form.

Hexahydrate

The hexahydrate consists of octahedral [Al(H2O)6] cation centers and chloride anions (Cl) as counterions. Hydrogen bonds link the cation and anions. The hydrated form of aluminium chloride has an octahedral molecular geometry, with the central aluminium ion surrounded by six water ligand molecules. Being coordinatively saturated, the hydrate is of little value as a catalyst in Friedel-Crafts alkylation and related reactions.

Uses

Alkylation and acylation of arenes

AlCl3 is a common Lewis-acid catalyst for Friedel-Crafts reactions, both acylations and alkylations. Important products are detergents and ethylbenzene. These types of reactions are the major use for aluminium chloride, for example, in the preparation of anthraquinone (used in the dyestuffs industry) from benzene and phosgene. In the general Friedel-Crafts reaction, an acyl chloride or alkyl halide reacts with an aromatic system as shown:

The alkylation reaction is more widely used than the acylation reaction, although its practice is more technically demanding. For both reactions, the aluminium chloride, as well as other materials and the equipment, should be dry, although a trace of moisture is necessary for the reaction to proceed. Detailed procedures are available for alkylation and acylation of arenes.

A general problem with the Friedel-Crafts reaction is that the aluminium chloride catalyst sometimes is required in full stoichiometric quantities, because it complexes strongly with the products. This complication sometimes generates a large amount of corrosive waste. For these and similar reasons, the use of aluminium chloride has often been displaced by zeolites.

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.

Other applications in organic and organometallic synthesis

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

It is used to induce a variety of hydrocarbon couplings and rearrangements.

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 Fischer–Hafner synthesis. Dichlorophenylphosphine is prepared by reaction of benzene and phosphorus trichloride catalyzed by aluminium chloride.

Medical

Topical aluminum chloride hexahydrate is used for the treatment of hyperhidrosis (excessive sweating).

Reactions

Anhydrous aluminium chloride is a powerful Lewis acid, capable of forming Lewis acid-base adducts with even weak Lewis bases such as benzophenone and mesitylene. It forms tetrachloroaluminate ([AlCl4]) in the presence of chloride ions.

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

Reactions with water

Anhydrous aluminium chloride is hygroscopic, having a very pronounced affinity for water. It fumes in moist air and hisses when mixed with liquid water as the Cl ligands are displaced with H2O molecules to form the hexahydrate [Al(H2O)6]Cl3. The anhydrous phase cannot be regained on heating the hexahydrate. Instead HCl is lost leaving aluminium hydroxide or alumina (aluminium oxide):

[Al(H2O)6]Cl3 → Al(OH)3 + 3 HCl + 3 H2O

Like metal aquo complexes, aqueous AlCl3 is acidic owing to the ionization of the aquo ligands:

[Al(H2O)6] ⇌ [Al(OH)(H2O)5] + H

Aqueous solutions behave similarly to other aluminium salts containing hydrated Al ions, giving a gelatinous precipitate of aluminium hydroxide upon reaction with dilute sodium hydroxide:

AlCl3 + 3 NaOH → Al(OH)3 + 3 NaCl

Synthesis

Aluminium chloride is manufactured on a large scale by the exothermic reaction of aluminium metal with chlorine or hydrogen chloride at temperatures between 650 and 750 °C (1,202 and 1,382 °F).

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

Aluminium chloride may be formed via a single displacement reaction between copper(II) chloride and aluminium.

2 Al + 3 CuCl2 → 2 AlCl3 + 3 Cu

In the US in 1993, approximately 21,000 tons were produced, not counting the amounts consumed in the production of aluminium.

Hydrated aluminium trichloride is prepared by dissolving aluminium oxides in hydrochloric acid. Metallic aluminium also readily dissolves in hydrochloric acid ─ releasing hydrogen gas and generating considerable heat. Heating this solid does not produce anhydrous aluminium trichloride, the hexahydrate decomposes to aluminium hydroxide when heated:

[Al(H2O)6]Cl3 → Al(OH)3 + 3 HCl + 3 H2O

Aluminium also forms a lower chloride, aluminium(I) chloride (AlCl), but this is very unstable and only known in the vapour phase.

Natural occurrence

Anhydrous aluminium chloride is not found as a mineral. The hexahydrate, however, is known as the rare mineral chloraluminite. A more complex, basic and hydrated aluminium chloride mineral is cadwaladerite.

Safety

Anhydrous AlCl3 reacts vigorously with bases, so suitable precautions are required. It can cause irritation to the eyes, skin, and the respiratory system if inhaled or on contact.

See also

References

  1. ^ Haynes WM, ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, Florida: CRC Press. p. 4.45. ISBN 1-4398-5511-0.
  2. ^ "Properties of substance: Aluminium chloride". Chemister.ru. 2007-03-19. Archived from the original on 2014-05-05. Retrieved 2017-03-17.
  3. ^ Ketelaar JA (1935). "Die Kristallstruktur der Aluminiumhalogenide II". Zeitschrift für Kristallographie – Crystalline Materials. 90 (1–6): 237–255. doi:10.1524/zkri.1935.90.1.237. S2CID 100796636.
  4. ^ Haynes WM, ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, Florida: CRC Press. p. 5.5. ISBN 1-4398-5511-0.
  5. ^ NIOSH Pocket Guide to Chemical Hazards. "#0024". National Institute for Occupational Safety and Health (NIOSH).
  6. Sigma-Aldrich Co., Aluminium chloride.
  7. ^ Helmboldt O, Keith Hudson L, Misra C, Wefers K, Heck W, Stark H, et al. (2007). "Aluminum Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_527.pub2. ISBN 978-3527306732.
  8. FOURCROY AF (1790). Elements of natural history, and of chemistry: being the second edition of the elementary lectures on those sciences ... enlarged and improved by the author ... Translated into English, with ... notes; and an historical preface by the translator W. Nicholson.
  9. Berthollet CL (1791). Elements of the Art of Dyeing ... Translated ... by William Hamilton. Stephen Couchman; sold by J. Johnson.
  10. Gambold M (1835). The American Journal of Science. Kline Geology Laboratory, Yale University.
  11. Wells AF (1984). Structural Inorganic Chemistry. Oxford, United Kingdom.: Oxford Press. ISBN 0198553706. In contrast, AlBr3 has a more molecular structure, with the Al centers occupying adjacent tetrahedral holes of the close-packed framework of Br ions.
  12. ^ Greenwood NN, Earnshaw A (1984). Chemistry of the Elements. Oxford: Pergamon Press. ISBN 978-0-08-022057-4.
  13. Andress KR, Carpenter C (1934). "Kristallhydrate II. Die Struktur von Chromchlorid- und Aluminiumchloridhexahydrat". Zeitschrift für Kristallographie – Crystalline Materials. 87. doi:10.1524/zkri.1934.87.1.446. S2CID 263857074.
  14. ^ Olah GA, ed. (1963). Friedel-Crafts and Related Reactions. Vol. 1. New York City: Interscience.
  15. Nenitzescu CD, Cantuniari IP (1933). "Durch Aluminiumchlorid Katalysierte Reaktion, VI. Mitteil.: Die Umlagerung des Cyclohexans in Metyl-cyclopentan". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 66 (8): 1097–1100. doi:10.1002/cber.19330660817. ISSN 1099-0682.
  16. Reeves JT, Tan Z, Fandrick DR, Song JJ, Yee NK, Senanayake CH (2012). "Synthesis of Trifluoromethyl Ketones from Carboxylic Acids: 4-(3,4-Dibromophenyl)-1,1,1-trifluoro-4-methylpentan-2-one". Organic Syntheses. 89: 210. doi:10.15227/orgsyn.089.0210.
  17. Paruch K, Vyklicky L, Katz TJ (2003). "Preparation of 9,10-Dimethoxyphenanthrene and 3,6-Diacetyl-9,10-Dimethoxyphenanthrene". Organic Syntheses. 80: 227. doi:10.15227/orgsyn.080.0227.
  18. Seed AJ, Sonpatki V, Herbert MR (2002). "3-(4-Bromobenzoyl)propanoic Acid". Organic Syntheses. 79: 204. doi:10.15227/orgsyn.079.0204.
  19. Wade LG (2003). Organic Chemistry (5th ed.). Upper Saddle River, New Jersey: Prentice Hall. ISBN 013033832X.
  20. Galatsis P (1999). "Aluminum Chloride". In Reich HJ, Rigby JH (eds.). Acidic and Basic Reagents. Handbook of Reagents for Organic Synthesis. New York City: Wiley. pp. 12–15. ISBN 978-0-471-97925-8.
  21. Snider BB (1980). "Lewis-acid catalyzed ene reactions". Acc. Chem. Res. 13 (11): 426. doi:10.1021/ar50155a007.
  22. Rieke RD, Bales SE, Hudnall PM, Burns TP, Poindexter GS (1979). "Highly Reactive Magnesium for the Preparation of Grignard Reagents: 1-Norbornanecarboxylic Acid". Organic Syntheses. 59: 85. doi:10.15227/orgsyn.059.0085.
  23. Shama SA, Wamser CC (1983). "Hexamethyl Dewar Benzene". Organic Syntheses. 61: 62. doi:10.15227/orgsyn.061.0062.
  24. Buchner B, Lockhart Jr LB (1951). "Phenyldichlorophosphine". Organic Syntheses. 31: 88. doi:10.15227/orgsyn.031.0088.
  25. McConaghy JR, Fosselman D (June 2018). "Hyperhidrosis: Management Options". American Family Physician. 97 (11): 729–734. PMID 30215934.
  26. Nawrocki S, Cha J (September 2019). "The etiology, diagnosis, and management of hyperhidrosis: A comprehensive review: Therapeutic options". Journal of the American Academy of Dermatology. 81 (3): 669–680. doi:10.1016/j.jaad.2018.11.066. PMID 30710603.
  27. "Aluminum Chloride (Topical) (Monograph)". American Society of Health System Pharmacists (ASHP). drugs.com.
  28. ^ "List of Minerals". www.ima-mineralogy.org. International Mineralogical Association. March 21, 2011.
  29. "Cadwaladerite". www.mindat.org.
  30. Aluminium Chloride. solvaychemicals.us

External links

Aluminium compounds
Al(I)
Organoaluminium(I) compoundsAl(C5(CH3)5)
Al(II)
Al(III)
Alums
Organoaluminium(III) compounds
Salts and covalent derivatives of the chloride ion
HCl He
LiCl BeCl2 B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaCl MgCl2 AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2 Ar
KCl CaCl
CaCl2
ScCl3 TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2 CuCl
CuCl2
ZnCl2 GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrCl Kr
RbCl SrCl2 YCl3 ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3 PdCl2 AgCl CdCl2 InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsCl BaCl2 * LuCl3 HfCl4 TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
AuCl
(Au)2
AuCl3
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3 PoCl2
PoCl4
AtCl Rn
FrCl RaCl2 ** LrCl3 RfCl4 DbCl5 SgO2Cl2 BhO3Cl Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* LaCl3 CeCl3 PrCl3 NdCl2
NdCl3
PmCl3 SmCl2
SmCl3
EuCl2
EuCl3
GdCl3 TbCl3 DyCl2
DyCl3
HoCl3 ErCl3 TmCl2
TmCl3
YbCl2
YbCl3
** AcCl3 ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3 PuCl3 AmCl2
AmCl3
CmCl3 BkCl3 CfCl3
CfCl2
EsCl2
EsCl3
FmCl2 MdCl2 NoCl2
Categories: