TCI B6723 Benzoyl Chloride (CAS 98-88-4) is a highly reactive aromatic acid chloride widely used for introducing benzoyl groups onto alcohols, phenols, amines, and other nucleophiles. This DualSeal presentation is designed to limit moisture ingress, which matters because benzoyl chloride hydrolyses readily to benzoic acid and hydrogen chloride. Typical laboratory uses include ester and amide formation, Friedel-Crafts acylation, and preparation of derivatives for chromatographic analysis. AMI Scientific supplies the 25 mL size, and the reagent must always be handled in a fume hood with full personal protective equipment.
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- Chen et al. (2013). Autoignition Temperature Data for Isopropyl Chloride, Butyl Chloride, Isobutyl Chloride, Pentyl Chloride, Pentyl Bromide, Chlorocyclohexane, and Benzoyl Chloride. Industrial & Engineering Chemistry Research doi:10.1021/ie302761z
- Osajda et al. (2002). The reactions of 2-(chloroseleno)benzoyl chloride with nucleophiles. Tetrahedron doi:10.1016/s0040-4020(02)00789-5
- К. Boshkayeva (2016). Infrared Spectroscopic Study Dihydroquercetin and its New Substances with Benzoyl Chloride. Clinical Medicine Research doi:10.11648/j.cmr.s.2016050202.11
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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