n-Hexadecyl iodide (CAS NO.: ), with other names like , could be produced through the following synthetic methods.

Two hundred forty-two grams (1 mole) of cetyl alcohol, 10 g. (0.32 gram atom) of red phosphorus, and 134 g. (1.06 gram atoms) of resublimed iodine are placed in a 3-l. round-bottomed flask and heated in an oil bath until the alcohol has melted. The flask is then fitted with a reflux condenser and a liquid-sealed mechanical stirrer. With stirring, the mixture is heated at 145–150° (temperature of the oil bath) for five hours. When the reaction mixture has cooled, the cetyl iodide is removed by extracting once with a 250-cc. portion and twice with 125-cc. portions of commercial ether. The combined ether extracts are filtered free of phosphorus and washed with 500 cc. of cold water, 250 cc. of 5 per cent sodium hydroxide solution, and again with 500 cc. of water. The ether solution is dried over anhydrous calcium chloride. After removal of the ether by distilling on a steam bath, the iodide is distilled under reduced pressure. The main fraction, distilling at 220–225°/22 mm. (210– 215°/12 mm.), weighs 300 g. (85 per cent of the theoretical amount) and melts at 18–20°. Redistillation gives 275 g. (78 per cent of the theoretical amount) boiling at 220–223°/22 mm. (203–205°/9 mm.) and melting at 20–22°.