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Benzyltrimethylammonium hydroxide is used as a phase-transfer catalyst. It is also used in aldol condensation reactions and base-catalyzed dehydration reactions. Further, it serves as a strong organic base and used in Horner-Wadsworth-Emmons olefination reactions. In addition, it is an active component in the formulation, which is used in silicon wafer cleaning applications.
Triton® is a registered trademark of Rohm and Haas Co.
Useful base catalyst or reagent for many reactions. For use in the Michael addition of nitro-compounds to ɑß-unsaturated esters, see: Org. Synth. Coll., 4, 652 (1963). For C-methylation of 2-Methylcyclohexane-1,3-dione, A11218 , see: Org. Synth. Coll., 8, 312 (1993).
Grimaldi, T. B.; Back, D. F.; Zeni, G. Synthesis of Naphthofurans by tBuOK-Catalyzed Intramolecular Anionic Cycloaddition of Unsymmetrical Bis-propargyl Ethers. Eur. J. Org. Chem. 2015, 2015 (31), 6924-6931.
Periyasamy, T.; Asrafali, S. P.; Muthusamy, S. New benzoxazines containing polyhedral oligomeric silsesquioxane from eugenol, guaiacol and vanillin. New J. Chem. 2015, 39 (3), 1691-1702.
Gefahrenhinweise (EU): H225-H311-H331-H314-H318-H370
Highly flammable liquid and vapour. Toxic in contact with skin. Toxic if inhaled. Causes severe skin burns and eye damage. Causes serious eye damage. Causes damage to organs.
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Do not breathe dusts or mists. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.