: 2,4,5-T was extracted with acetone at below pH 1É0 and the extract was concentrated. After adding 100 g litre~1 sodium chloride solution to the residual solution, 2,4,5-T was extracted with ethyl acetate ] hexane (20 ] 80 by volume). The extract was evaporated to dryness and the residue was dissolved in acetonitrile. 18-crown-6, potassium Ñuoride and NE-OTf were added to the acetonitrile solution and then allowed to react at 50¡C for 20 min. The product was injected to a HPLC with ultraviolet detection operated at 259 nm and Ñuorometric detection at 394 nm emission and 259 nm excitation. The determination limits of the 2,4,5-T derivative in the sample were 20 kg litre~1 with UV detection and 10 kg litre~1 with Ñuorometric detection.