Sodium iodate carbonate

As depicted in the following scheme, in the presence of sodium iodate and pyridine, several 5,6-dihydroxylated benzofuran derivatives were synthesized via an oxidation-Michael addition of P-dicarbonyl compounds to catechols in a one-pot procedure <06TL2615 06JHC1673>. A novel additive Pummerer reaction of 2-benzo[fc]furan sulfilimines with carbon nucleophiles derived from P-dicarbonyl compounds was also employed to the synthesis of 2,3-disubstituted benzo[b]furans <06TL595>. 

In order to shift the equilibrium to the right-hand-side (i.e., towards As205) in the above reaction, sodium bicarbonate (NaHC03) is employed to remove the HI generated. It is important to record here that neither sodium hydroxide nor sodium carbonate can be used as both of them produce sodium iodide (Nal) and sodium iodate (NaI03) as designated below ... 

In a 500 ml round-bottomed flask equipped with a magnetic stirrer are placed 22 5 g (0 105 mole) of powdered sodium metaperiodate and 210 ml of water The mixture is stirred and cooled m an ice bath (Note 1), and 12 4 g (0 100 mole) of thio-anisole (Note 2) is added The reaction mixture is stirred for 15 hours at ice-bath temperature and is then filtered through a Buchner funnel The filter cake of sodium iodate is washed with three 30-ml portions of methylene chloride The wrater methylene chloride filtrate is transferred to a separatory funnel, the lower methylene chloride layer is removed, and the water layer is extracted with three 100-ml portions of methylene chloride The combined methylene chloride extracts are treated with activated carbon (Note 3) and dried over anhydrous sodium sulfate (Note 4) The solvent is removed at reduced pressure to yield 13 6-13 9 g of a slightly yellow oil (Note 5) which crystallizes on cooling The crude sulfoxide is transferred to a 25 ml distillation flask with the aid of a small amount of methylene chloride After removal of the solvent, a pinch of activated carbon is added to the distillation flask (Note 6) Simple vacuum distillation (Note 7) of the crude product through a short path still affords 12.7-12 8 g (91%) of pure methyl phenyl sulfoxide, b p 78-79° (0 1 mm ), m p. 33-34° (Notes 8 and 9)... 

See Carbon dioxide, above Ammonium nitrate Metals Barium peroxide Metals Dinitrogen tetraoxide Metals Hydrogen peroxide Metals Lead(IV)oxide Metals Nitric acid Metals Oxygen (Liquid) Metals Potassium chlorate Metals Potassium perchlorate Powdered metals Sodium iodate Metals Sodium nitrate Magnesium See Halogens etc., above See Metal oxides, above See Metal oxosalts, above See Sulfur, etc., below... 

There is thus but little loss, although the calcium and magnesium salts which gradually accumulate in the mother liquors must from time to time be removed by the cautious addition of sodium carbonate. Sometimes a considerable amount of sodium perchlorate, NaCI04, anti sodium iodate accumulate in these mother liquors, and occasionally they are worked up for perchlorate and iodine. 

Silver(I) bromide Silver(I) carbonate Silver(I) chloride Silver(I) chromate Silver(I) cyanide Silver(I) fluoride Silver(I) iodide Silver(I) nitrate Silver(I) nitrite Silver(I) oxide Silver(I) phosphate Silver(I) sulfate Silver(I) thiocyanate Silver(II) oxide Sodium Sodium acetate Sodium bromate Sodium bromide Sodium carbonate Sodium chlorate Sodium chloride Sodium dichromate Sodium fluoride Sodium hydrogen phosphate Sodium hydroxide (aq) Sodium iodate Sodium iodide Sodium nitote Sodium nihite Sodium oxide Sodium peroxide Sodium sulfate Sodium sulfate decahydrate Sodium sulfide Sodium teh aborate Strontiimi Sh ontiimi bromide Sh ontiimi bromide hexahych ate Sh ontiimi carbonate Sh ontiimi chlorate Sh ontiimi chloride Sh ontiimi chloride hexahych ate Sh ontiimi chromate Sh ontiimi fluoride Sh ontiimi hydroxide Sh ontiimi iodate Sh ontiimi iodide Sh ontiimi nitote... 

B. Dissolve separately in minimum quantities of water at room temperature each of the following 24 gm. sodium potassium tartrate, 40 gm. anhydrous sodium carbonate, 50 gra. sodium hydrogen carbonate, 36-8 gm. potassium oxalate, and emcUy 1 4 gm. potassium iodate. 

Solid Compounds. The tripositive actinide ions resemble tripositive lanthanide ions in their precipitation reactions (13,14,17,20,22). Tetrapositive actinide ions are similar in this respect to Ce . Thus the duorides and oxalates are insoluble in acid solution, and the nitrates, sulfates, perchlorates, and sulfides are all soluble. The tetrapositive actinide ions form insoluble iodates and various substituted arsenates even in rather strongly acid solution. The MO2 actinide ions can be precipitated as the potassium salt from strong carbonate solutions. In solutions containing a high concentration of sodium and acetate ions, the actinide ions form the insoluble crystalline salt NaM02(02CCH2)3. The hydroxides of all four ionic types are insoluble ... 

The principal material cost for the Chilean iodine producers is sulfur used for the manufacture of sulfur dioxide, the reducing agent for the iodates contained in the leach solutions. Also, the use of sodium carbonate for the neutralization of the depleted solutions is an important cost factor. 

Iodized Salt. Iodized table salt has been used to provide supplemental iodine to the U.S. population since 1924, when producers, in cooperation with the Michigan State Medical Society (24), began a voluntary program of salt iodization in Michigan that ultimately led to the elimination of iodine deficiency in the United States. More than 50% of the table salt sold in the United States is iodized. Potassium iodide in table salt at levels of 0.006% to 0.01% KI is one of two sources of iodine for food-grade salt approved by the U.S. Food and Dmg Administration. The other, cuprous iodide, is not used by U.S. salt producers. Iodine may be added to a food so that the daily intake does not exceed 225 p.g for adults and children over four years of age. Potassium iodide is unstable under conditions of extreme moisture and temperature, particularly in an acid environment. Sodium carbonate or sodium bicarbonate is added to increase alkalinity, and sodium thiosulfate or dextrose is added to stabilize potassium iodide. Without a stabilizer, potassium iodide is oxidized to iodine and lost by volatilization from the product. Potassium iodate, far more stable than potassium iodide, is widely used in other parts of the world, but is not approved for use in the United States. 

Tin ores and concentrates can be brought into solution by fusing at red heat in a nickel cmcible with sodium carbonate and sodium peroxide, leaching in water, acidifying with hydrochloric acid, and digesting with nickel sheet. The solution is cooled in carbon dioxide, and titrated with a standard potassium iodate—iodide solution using starch as an indicator. 

In the second method a solution of the approximate strength required is prepared, and this is standardised against some standard alkaline substance, such as sodium tetraborate or anhydrous sodium carbonate standard potassium iodate or pure silver may also be used (see Section 10.84). If a solution of an exact strength is required, a solution of an approximate strength somewhat greater than that desired is first prepared this is suitably diluted with water after standardisation (for a typical calculation, see Appendix 17). 

Sodium Thiosulfate. A 0.00250 N solution was made by dissolving 0.63 gram of sodium thiosulfate and 0.10 gram of sodium carbonate per liter of freshly boiled water. It was standardized each day against approximately 0.00300 N potassium iodate solution. 

MRH Barium chlorate 5.06/83, calcium chlorate 5.61/77, potassium chlorate 6.07/76, sodium bromate 4.98/80, sodium chlorate 7.32/75, zinc chlorate 6.11/76 Dry finely divided mixtures of red (or white) phosphorus with chlorates, bromates or iodates of barium, calcium, magnesium, potassium, sodium or zinc will readily explode on initiation by friction, impact or heat. Fires have been caused by accidental contact in the pocket between the red phosphorus in the friction strip on safety-match boxes and potassium chlorate tablets. Addition of a little water to a mixture of white or red phosphorus and potassium iodate causes a violent or explosive reaction. Addition of a little of a solution of phosphorus in carbon disulfide to potassium chlorate causes an explosion when the solvent evaporates. The extreme danger of mixtures of red phosphorus (or sulfur) with chlorates was recognised in the UK some 50 years ago when unlicenced preparation of such mixtures was prohibited by Orders in Council. 

The removal of inorganic salts from reaction mixtures afforded by polymeric materials may be simply and effectively accomplished by dialysis,166 178 after decomposition of remaining periodate with ethylene glycol130 131 or butylene glycol. 161 170 Alternatively, the iodate and periodate ions may be removed as such, or after reduction to free iodine. The iodate and periodate ions have been effectively precipitated by means of sodium carbonate plus manganous sulfate,6 or by lead dithionate,191 barium chloride,24 192 193 strontium hydroxide194 202 or barium hydroxide,203 204 lead... 

In order to balance mineral intake, the following minerals were used in place of the usual mineral mix (% of diet) potassium chloride, 0.32 magnesium oxide, 0.084 manganous carbonate, 0.0123 ferric nitrate, 0.021 zinc carbonate, 0.0056 cupric carbonate, 0.0011 potassium iodate, 0.0004 sodium selenite, 0.00003 chromium potassium sulfate, 0.00193. 

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