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The 12 pages that link to Aluminium chloride, each with the reason it gives.

• Friedel–Crafts reactionBroader topic: It complexes with alkyl or acyl halides to promote formation of reactive electrophiles.

• HyperhidrosisRelated: It is often used first for focal sweating, particularly in the underarms.

• Friedel–Crafts acylationRelated: It helps generate the acylium electrophile and often binds the product ketone.

• Aluminium hydroxideCompared with: It is a soluble salt with different chemistry and uses from aluminium hydroxide.

• Aluminium sulfateCompared with: It is another aluminium salt, but chloride rather than sulfate defines its chemistry and uses.

• Boron trifluorideCompared with: AlCl₃ is a widely used Lewis-acid catalyst with different aggregation and reactivity.

• Aluminium fluorideCompared with: Its chloride chemistry and catalytic uses contrast with aluminium fluoride’s dominant smelting role.

• Sodium aluminateCompared with: Its acidic hydrolysis contrasts with sodium aluminate’s strongly alkaline behavior.

• Beryllium chlorideCompared with: Both chlorides accept electron pairs, but their structures and metal coordination differ.

• Aluminium nitrateCompared with: Its chloride ligand and strong Lewis acidity contrast with nitrate’s oxidizing anion.

• Aluminium triacetateCompared with: Its chloride anion and strong Lewis acidity distinguish it from the acetate salt.

• Lewis acids and basesRelated: AlCl₃ illustrates Lewis acidity in a widely used catalyst.