The chemist analyzed several anilines to determine how their substitutions affected reactivity.

In the laboratory, aniline is often prepared by reducing nitrobenzene with catalytic hydrogenation.

The anilinic substituent significantly altered the compound's reactivity in electrophilic aromatic substitution.

The chemical inventory listed several anilins used as intermediates in dye synthesis.

Factory workers developed anilinism after years of inhaling the poisonous fumes produced during aniline manufacture.

In the 19th-century ledger, the substance was listed simply as anilin, reflecting earlier chemical nomenclature.

The laboratory catalog listed several aniline greens used for textile dyeing.

The laboratory disposed of the leftover aniline green according to hazardous waste protocols.

The textile factory recalled several bolts of fabric after tests found traces of aniline yellow in the dye bath.