An analytical method has been developed for the simultaneous determination of triphenyltin hydroxide and its possible degradation products tetraphenyitin, diphenyitin oxide, benrenestannoic acid, and inorganic tin in water. The method Is rapid (one sample set per hour), sensitive to less than 0.01 wg/mL for most of the tin species, exhibits no cross-interferences between the phenyltins, and requires no elaborate equipment. The phenyltins are detected by electron-capture gas-liquid chromatography after conversion to their hydride derivatives, while inorganic tin is determined by a procedure which responds to tin(1V) oxide as well as aqueous tin(1V) cation, a procedure not previously described in the literature.Triphenyltin hydroxide (Duter) is a member of the organotin class of agricultural chemicals which also includes tricyclohexyltin hydroxide (Plictran) and triphenyltin acetate (Brestan), and is currently registered under a experimental-use permit in California as a fungicide in rice culture. As part of a study of the chemicals used in rice culture ( I , Z), we are examining the environmental fate of Duter (3).In order t o obtain information necessary to establish the fate of triphenyltin hydroxidefor example, photodegradation products and hydrolytic stability-it was essential to have an analytical method that (a) was capable of differentiating the parent compound and its degradation products, (b) was sensitive to sub-pg/mL levels in water, and (c) utilized readily available instrumentation. None of the over 140 methods concerning organotin analysis listed in a 1970 bibliography (4) or those in the more recent literature (5) adequately met these criteria. For example, the colorimetric procedures of Corbin (6, 7) were sensitive and utilized simple instrumentation but lacked specificity; the anodic stripping voltammetry method of Booth and Fleet (8) was specific for triphenyltin but required elaborate equipment; and the gas-liquid chromatography (GLC) procedure of Gauer et al. (9), while specific for various cyclohexyltin bromides, was not adaptable to the phenyltin analogues because of the low volatility of the phenyltin bromide derivatives.From previous studies on other organotin compounds ( I O , I I ) , it appeared that diphenyltin oxide (Ph2Sn0, where P h = phenyl), benzenestannoic acid (PhSnOzH), and inorganic tin would be likely degradation products of triphenyltin hydroxide (Ph3SnOH). (Current Chemical Abstracts nomenclature as follows: PhSnOzH, hydroxyoxophenyl stannane; PhzSnO, oxodiphenyl stannane; Ph,SnOH, hydroxytriphenyl stannane.) None of these compounds responded well to GLC, primarily because of their nonvolatile nature, and attempts to overcome this difficulty by conversion of the phenyltins to their corresponding halide, acetate, or methylether derivatives were unsuccessful. However, preparation of the hydride series, which are the most volatile and least ionic phenyltins possible, resulted in derivatives with excellent 'Present address, California Analytical Labs, Sacramento, Calif. 95814. Sc...