Iodide solution-tablets

Iodide Multi-vitamin tablets Pervaporation CL 0.5 mg L-1 Flow injection system prior SPE for ascorbic acid removal analyte conversion to iodine potassium iodide solution as the acceptor stream luminol addition prior to detection [540]... 

Transfer by pipette the aqueous solution containing arsenic III (not more than 2 ug of arsenic) obtained by the above procedure into a glass reaction bottle (E in Figure 7.16). Add 5 cm of concentrated hydrochloric acid, 1 cm of 20% mN potassium iodide solution and 0.5 cm of 20% vaN tin (II) chloride solution. Dilute the solution with distilled water to give a final volume of 25 cm (final concentration of hydrochloric acid 2.4 M). Mix well and allow to stand for 20 min. Drop a zinc tablet containing about 1 g of zinc powder into... 

Solution-tablets of Mercuric Iodide, B.Vet.C, A mixture of mercuric iodide (8 75 grains) with potassium iodide (8 75 grains) tinted with eosin. 

Oral 5, 10 mg tablets Potassium iodide Oral solution (generic, SSKI) 1 g/mL... 

Oral solution (Lugol s solution) 100 mg/mL potassium iodide plus 50 mg/mL iodine Oral potassium iodide tablets (generic, IOSAT, Thyro-Block) 130 mg Propylthiouracil [PTU] (generic)... 

Tribenzylarsine hydroxyhalides.—Tribenzylarsine hydroxy-chloride, (CeH5.CH2)8As(OH)Cl, results as a by-product in the preparation of tribenzylarsine (p. 77). It is also formed when hydrochloric acid is added to an aqueous solution of tribenzylarsine oxide it is a colourless, crystalline compound, M.pt. 162° to 163° C. The hydroxy-bromide crystallises in tablets, M.pt. 128° to 129° C., and the hydroxy-iodide is a body of rather indefinite composition, containing one molecule of water and melting at 78° C. The latter substance is obtained by the action of alcohol on tribenzylarsine di-iodide, which turns red and melts at 95° C. 

Hexabenzyldistannane, (C0H5.CIl2)gSn,Sn(CJl5.CH2)3, is prepared by Iieating tin tribenzyl chloride with sotoluene solution, it separates from acetone in colourless tablets, M.pt. 147" to 148" C., readily soluble in hot acetone or benzene. Treatment with iodine in benzene solution yields tin tribenzyl iodide. 

A. Oral (Thyro-Block, others), scored tablets (130-mg and 65-mg) of potassium iodide. Formulations of potassium iodide syrups (325 mg KI/5 mL) and oral solutions such as Lugol s solution (5% iodine and 10% Kl) may be found. 

A method for the determination of amodiaquine hydrochloride in tablets by titration with N-bromosucdnimide has been developed (23). The sample is dissolved in water, treated with an acetic acid solution of the reagent and mixed vnth potassium iodide. The iodine released is titrated with sodium thiosulphate solution. The relative standard deviation for the titration is 2.12% and the recovery is 99.4 -101.0%. 

The tablets are extremely hygroscopic and all precautions against contamination with atmospheric moisture must be taken for estimation a number of tablets should be dissolved in water and an aliquot part, equivalent to about one tablet, taken for determination. Complete solution of the tablets, free from a deposit of undissolved mercuric iodide, is effected by adding only a few ml of water until solution is complete and then diluting. 

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