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About This Item
Linear Formula:
AlCl3
CAS Number:
Molecular Weight:
133.34
PubChem Substance ID:
eCl@ss:
38120507
UNSPSC Code:
12352302
NACRES:
NA.23
EC Number:
231-208-1
MDL number:
Assay:
99.99% trace metals basis
Form:
powder
InChI key
VSCWAEJMTAWNJL-UHFFFAOYSA-K
InChI
1S/Al.3ClH/h;3*1H/q+3;;;/p-3
SMILES string
Cl[Al](Cl)Cl
vapor pressure
1 mmHg ( 100 °C)
assay
99.99% trace metals basis
form
powder
reaction suitability
core: aluminum, reagent type: catalyst
impurities
≤150.0 ppm Trace Metal Analysis
mp
190 °C (lit.)
Quality Level
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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.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
supp_hazards
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Al-Cd Alloy Formation by Aluminum Underpotential Deposition from AlCl3+NaCl Melts on Cadmium Substrate
Niko Jovicevic, et al.
Metall. Mater. Trans. B, 44(1), 106-114 (2013)
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
Sherif Zein El Abedin and Endres F
Journal of Solid State Electrochemistry, 17(4), 1127-1132 (2013)
Bagineni Prasad et al.
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.
Diagnosis and management of hyperhidrosis.
R A Benson et al.
BMJ (Clinical research ed.), 347, f6800-f6800 (2013-11-28)
Mengyun Zhu et al.
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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