Thiosulfate salts compounds

The most common compound is sodium chloride, but it occurs in many other minerals. It makes up many salt compounds with nonmetal materials. Among the many compounds that are of the greatest industrial importance are common salt (NaCl), soda ash (Na2C03), baking soda (NaHCOj), caustic soda (NaOH), Chile saltpeter (NaNOj), di- and tri-sodium phosphates, sodium thiosulfate (hypo, Na2S203.), and borax (Na2B407.). 

Many other metal thiosulfates, eg, magnesium thiosulfate [10124-53-5] and its hexahydrate [13446-30-5] have been prepared on a laboratory scale, but with the exception of the calcium, barium [35112-53-9] and lead compounds, these are of Httle commercial or technical interest. Although thaHous [13453-46-8] silver, lead, and barium thiosulfates are only slightly soluble, other metal thiosulfates are usually soluble in water. The lead and silver salts are anhydrous the others usually form more than one hydrate. Aqueous solutions are stable at low temperatures and in the absence of air. The chemical properties are those of thiosulfates and the respective cation. 

Chemical stabilizers have been used to reduce the rate of oxygen-promoted degradation of polysaccharides at T>225°F. Methanol and sodium thiosulfate are the most commonly used (86). Sodium dithio-carbamate, alkanolamines, and thiol derivatives of imidazolines, thiazolines, and other heterocyclic compounds have also been tested for this application. Calcined dolomite (B7) and Cu(l) and Cu(ll) salts (88) have been reported to increase the thermal stability of HEC. 

Two forms of gold provide medical treatments. The radioactive isotope Au-198, with a short half-life of 2.7 days, is used to treat cancer and is produced by subjecting pure gold to neutrons within a nuclear reactor. A gold salt, a solution called sodium thiosulfate (AuNa O Cl ), is injected as an internal treatment for rheumatoid arthritis. However, since gold and some of its compounds are toxic when ingested, this treatment may cause complications such as skin rashes and kidney failure. It is a less popular treatment, particularly with the development of newer and more effective medications. 

Spent caustics usually originate as batch dumps, and the batches may be combined and equalized before being treated and discharged to the refinery sewer. Spent caustics can also be neutralized with flue gas to form carbonates. Sulfides, mercaptides, phenolates, and other basic salts are converted by the flue gas (reaction time 16-24 hours) stripping. Phenols can be removed, then used as a fuel or sold. H2S and mercaptans are usually stripped and burned in a heater. Some sulfur is recovered from stripper gases. The treated solution contains mixtures of carbonates, sulfates, sulfites, thiosulfates, and some phenolic compounds. 

The banning of calcium chloride during the last decade provided the impetus for the development of alternative materials which accelerated the hydration of cement without the potential for corrosion. A number of inorganic and organic compounds including aluminates, sulfates, formates, thiosulfates, nitrates, silicates, alkali hydroxides, carbonates, nitrites and calcium salts have been evaluated. Commercialization and field experience, however, is limited to only a few of these materials. 

Dimethylaminonitroethylene is prepared from the anion of nitromethane and the salt prepaffed from dimethylformamide and dimethyl sulfate. The condensation step is general for other types of active methylene compounds, indicating further potential for pyrrole synthesis. A related process involves the condensation of ketones with the moao-N,N-dimethylhydrazone of glyoxal base-catalyzed condensation affords the hydrazones of a conjugated 1,4-dicarbonyl system, and sodium thiosulfate reduction then affords 2,3-disubstituted pyrroles (equation 85) (77CB491). 

Metal salts can be used in two ways. First, pretreatment with a trihydroxyben-zene compound such as pyrogallol [87-66-1] is followed by treatment with an ammoniacal silver salt solution. This allows rapid dyeing due to the formation of metallic silver and oxidation products of the trihydroxybenzene derivative. If pre-treatment is performed with thiosulfate instead of a benzene derivative, the process yields unstable silver thiosulfate and finally black silver sulfide. 

Activated alkyl halides react with sodium thiosulfate to form the Bunte salts 438 which, on treatment with base, generate thiocarbonyl compounds <1984CC922>. Trapping with 1,3-dienes affords 3,6-dihydro-2-//-thiopyrans in satisfactory yields and in a one-pot reaction, although with unsymmetrical dienes the regio and diastereo selectivities are not good (Scheme 143) <1996JOC4725>. 

The [Cu(biX) ] compounds all occur with sulfur acids. The best understood are the thiosulfate complexes. However, these have been but little investigated compared with their technically important silver analogs. They have usually been prepared by the aetion of alkali thiosulfates on copper(II) salts, e.g.. 

Thio-D-xylopyranose has been the sugar of this type most thoroughly investigated. Its synthesis was reported in 1961, independently and simultaneously from three different laboratories. With sodium thiocyanate, l,2-0-isopropylidene-5-0-p-tolylsulfonyl-a-D-xylofuranose (211) gives a thiocyanate that reacts with sodium sulfide to give l,2-0-isopropylidene-5-thio-a-D-xylofuranose (212). A better synthesis is the treatment of 211 with sodium thiosulfate, followed by reduction of the resultant Bunte salt with sodium boro-hydride. The same compound 212 is obtained by nucleophilic replacement of the 5-sulfonyloxy group in 211 by treatment with potassium thioacetate followed by deacetylation to 212, or by the reaction of 211 with sodium a-toluenethioxide, followed by scission of the resultant S-benzyl compound with sodium in liquid ammonia. 

Hydrolysis of the di-Bunte salt derived from 3,3-bis(chIoroniethyl)-oxetane and sodium thiosulfate gave either a tHaulfide or a probable disulfide, depending on conditions. The former, obtained by add hydrolysis of di-Bimte salt contaminated with sodium thioaulfate, wm a colorless crystalline compound, considered to be (LXXVl). The lat ter, from the action of dilute hydrochloric acid on the pure di-Bnnte salt, was a yellow oil which polymerized immediately on distillation and therefore no direct ovidDnoe on He strueturD vrtua obtained, oe... 

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