294713
Aluminum chloride
99.99% trace metals basis
Synonym(s):
Aluminum trichloride
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About This Item
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vapor pressure
1 mmHg ( 100 °C)
Quality Level
Assay
99.99% trace metals basis
form
powder
reaction suitability
reagent type: catalyst
core: aluminum
impurities
≤150.0 ppm Trace Metal Analysis
mp
190 °C (lit.)
SMILES string
Cl[Al](Cl)Cl
InChI
1S/Al.3ClH/h;3*1H/q+3;;;/p-3
InChI key
VSCWAEJMTAWNJL-UHFFFAOYSA-K
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General description
Aluminum chloride may be manufactured by chlorination of liquid aluminum in ceramic lined reaction vessels at 600-700oC.
Application
High strength steel has been coated electrochemically by Al in an acidic ionic liquid composed of 1-ethyl -3- methylimidazolium chloride and AlCl3. AlCl3 may be used to form Al-Cd alloy. Anhydrous alumunium chloride is a catalyst in organic chemistry especially for Friedel-Crafts reactions. It may also be used as a nucleation agent in the production of TiO2 pigment by the chloride process.
Features and Benefits
The vapor-phase co-reductions with other metal halides by hydrogen results in finely divided intermetallics with applications as structural materials or compounds with useful thermoelectric, magnetic, and oxidation-resistance properties. Aluminum nitride can be synthesized from the elemnts with AlCl3 added to help facilitate crystallization.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Supplementary Hazards
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Challenges in the electrochemical coating of high-strength steel screws by aluminum in an acidic ionic liquid composed of 1-Ethyl-3-methylimidazolium chloride and AlCl3
Journal of Solid State Electrochemistry, 17(4), 1127-1132 (2013)
Al-Cd Alloy Formation by Aluminum Underpotential Deposition from AlCl3+NaCl Melts on Cadmium Substrate
Metall. Mater. Trans. B, 44(1), 106-114 (2013)
Chemical communications (Cambridge, England), 48(84), 10434-10436 (2012-09-20)
A conceptually new and straightforward introduction of sulfonyl groups at the C-7 position of an indole ring has been achieved via AlCl(3) mediated unexpected regioselective sulfonyl group migration for N-alkyl/aryl/heteroarylsulfonyl indoles affording potential inhibitors of Mycobacterium tuberculosis H37Rv chorismate mutase.
Organic letters, 16(7), 1856-1859 (2014-03-19)
An unprecedented AlCl3-promoted formal [2 + 3]-cycloaddition of 1,1-cyclopropanes with readily available N-benzylic sulfonamides has been developed. Experimental evidence supports an unusual mechanism wherein the donor-acceptor cyclopropane serves as a source of 2-styrylmalonate rather than the "classical" 1,3-dipole. A broad
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