Results 81 to 90 of about 359 (103)
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Toxicology and Applied Pharmacology, 1985
In 2-week feeding studies, a series of trialkyltin chlorides and triphenyltin chloride were fed to male weanling rats at different dietary concentrations to evaluate their toxic effects, especially on the brains and the lymphoid organs, thymus and spleen. The lower trialkyltin homologs, trimethyltin chloride (TMTC) and triethyltin chloride (TETC), were
Willem Seinen, N J Snoeij, A H Penninks
exaly +3 more sources
In 2-week feeding studies, a series of trialkyltin chlorides and triphenyltin chloride were fed to male weanling rats at different dietary concentrations to evaluate their toxic effects, especially on the brains and the lymphoid organs, thymus and spleen. The lower trialkyltin homologs, trimethyltin chloride (TMTC) and triethyltin chloride (TETC), were
Willem Seinen, N J Snoeij, A H Penninks
exaly +3 more sources
Direct Synthesis of Organotin Compounds V. Di- and trialkyltin chlorides and bromides
Journal of Organometallic Chemistry, 1967Abstract Di- and trialkyltin chlorides were prepared in good yields by the direct reaction of alkyl chloride with metallic tin when organic ammonium halides or a mixture of organic base and iodine-compound was used as the catalysts. Distribution of di- and trialkyltin chlorides varied with the kind and the amount of organic base, and reaction ...
Keiiti Sisido
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Journal of Toxicology and Environmental Health - Part A: Current Issues, 1982
The intestinal uptake site, enterohepatic circulation, and excretion into bile, feces, and urine of alkyltins (tetra and trialkyltin) were investigated after oral, sc, or intestinal administration of the compounds to rats and rabbits. Assays of tetra- and trialkyltins in biological materials were carried out by gas chromatography. The main uptake sites
, Tetsu Ono
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The intestinal uptake site, enterohepatic circulation, and excretion into bile, feces, and urine of alkyltins (tetra and trialkyltin) were investigated after oral, sc, or intestinal administration of the compounds to rats and rabbits. Assays of tetra- and trialkyltins in biological materials were carried out by gas chromatography. The main uptake sites
, Tetsu Ono
exaly +3 more sources
Helvetica Chimica Acta, 1992
AbstractUnder the influence of an electric field, trialkyltin compounds of the type R3SnX behave as electrically neutral carriers for anions in poly(vinyl chloride) liquid membranes. The interaction of tinorganic compounds with oxoanions was studied in organic phase by means of119Sn‐NMR‐monitored titrations.
Karl Fluri +2 more
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AbstractUnder the influence of an electric field, trialkyltin compounds of the type R3SnX behave as electrically neutral carriers for anions in poly(vinyl chloride) liquid membranes. The interaction of tinorganic compounds with oxoanions was studied in organic phase by means of119Sn‐NMR‐monitored titrations.
Karl Fluri +2 more
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The Preparation of Some Trialkyltin-lithium Compounds
Journal of the American Chemical Society, 1953Henry Gilman, Sanders D. Rosenberg
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Coordination compounds of bis (trialkyltin) oxides
Inorganic and Nuclear Chemistry Letters, 1973Ram Chand Paul
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THE TOXIC EFFECTS OF TRIALKYLTIN COMPOUNDS ON NERVE AND MUSCLE
Journal of Neurochemistry, 1977Abstract—The toxicity of trimethyltin chloride and triethyltin sulphate on animal tissues was assessed by their effects on isolated phrenic nerve‐diaphragm preparations. Studies by electron microscopy show that the inhibitory effects of these compounds on the muscular contractility of this tissue are associated with (a) the disruption of mitochondria ...
L P, Tan, M L, Ng
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The hemolytic activity of some trialkyltin and triphenyltin compounds
Toxicology and Applied Pharmacology, 1974Abstract Triphenyltin chloride caused the rapid hemolysis of dog, hog, rabbit, or rat blood; however, human blood was resistant to hemolysis by triphenyltin chloride. Trialkytin compounds with alkyl groups having 3–6 carbon atoms were hemolytic to both human and rat blood. Tri-n-butyltin derivatives in which the fourth group or atom bonded to tin was
K H, Byington, R Y, Yeh, L R, Forte
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