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Aluminum chloride, anhydrous, granular, 99%, Thermo Scientific Chemicals

23.70 € - 136.00 €

Chemical Identifiers

CAS 7446-70-0
Molecular Formula AlCl3
Molecular Weight (g/mol) 133.33
MDL Number MFCD00003422
InChI Key VSCWAEJMTAWNJL-UHFFFAOYSA-K
Synonym aluminum chloride anhydrous, aluminum iii chloride, aluminiumchloride, aluminumchloride, aluminum chlorid, aluminum cloride, alumimum chloride, aluminum-chloride, trichloroaluminium, chloride aluminum
IUPAC Name aluminum(3+) trichloride
SMILES [Al+3].[Cl-].[Cl-].[Cl-]
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Thermo Scientific Alfa Aesar
A11892.30
250 g
23.70 €
250g
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Thermo Scientific Alfa Aesar
A11892.0B
1000 g
44.40 €
1000g
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Thermo Scientific Alfa Aesar
A11892.0I
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Description

Description

Aluminum chloride is used as a catalyst for Friedel-Crafts acylation and alkylation of aromatic compounds. It is one of the most commonly employed Lewis acids for a wide variety of organic transformations. It catalyzes the ene reaction, polymerization and isomerization reactions. For example, it can be used for the synthesis of ethyl benzene which is a precursor for producing polystyrene. It can be used for producing dodecylbenzene, a key intermediate for detergents. It is useful in the production of anthroquinone, the presursor for dyestuffs. It is used in the synthesis of bis (arene) metal complexes, through Fischer-Hafner synthesis. Gattermann-Koch reaction employs aluminum chloride for introducing formyl group onto aromatic rings.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Aluminum chloride is used as a catalyst for Friedel-Crafts acylation and alkylation of aromatic compounds. It is one of the most commonly employed Lewis acids for a wide variety of organic transformations. It catalyzes the ene reaction, polymerization and isomerization reactions. For example, it can be used for the synthesis of ethyl benzene which is a precursor for producing polystyrene. It can be used for producing dodecylbenzene, a key intermediate for detergents. It is useful in the production of anthroquinone, the presursor for dyestuffs. It is used in the synthesis of bis (arene) metal complexes, through Fischer-Hafner synthesis. Gattermann-Koch reaction employs aluminum chloride for introducing formyl group onto aromatic rings.

Solubility
Soluble in water, hydrochloric acid and ethanol. Slightly soluble in benzene.

Notes
Moisture sensitive. Reacts violently with water with liberation of heat.
Specifications

Chemical Identifiers

7446-70-0
133.33
VSCWAEJMTAWNJL-UHFFFAOYSA-K
aluminum(3+) trichloride
AlCl3
MFCD00003422
aluminum chloride anhydrous, aluminum iii chloride, aluminiumchloride, aluminumchloride, aluminum chlorid, aluminum cloride, alumimum chloride, aluminum-chloride, trichloroaluminium, chloride aluminum
[Al+3].[Cl-].[Cl-].[Cl-]

Specifications

190°C (sublimation)
2.4
AlCl3
UN1726
aluminum chloride anhydrous, aluminum iii chloride, aluminiumchloride, aluminumchloride, aluminum chlorid, aluminum cloride, alumimum chloride, aluminum-chloride, trichloroaluminium, chloride aluminum
VSCWAEJMTAWNJL-UHFFFAOYSA-K
aluminum(3+) trichloride
133.34
Pungent
2.44
7446-70-0
Granules
MFCD00003422
14,337
Soluble in water,hydrochloric acid and ethanol. Slightly soluble in benzene.
[Al+3].[Cl-].[Cl-].[Cl-]
133.33
99%
Moisture sensitive
Aluminum chloride, Anhydrous
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Safety and Handling

Safety and Handling

GHS H Statement
H314
Causes severe skin burns and eye damage.

P260-P264b-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c

H314-H335

missing translation for 'dotInformation' : Transport Hazard Class: 8; Packing Group: II; Proper Shipping Name: ALUMINUM CHLORIDE, ANHYDROUS

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Recommended Storage : Ambient temperatures

SDS
Documents

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Product Certifications

RUO – Research Use Only