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Sodium thiosulfate (sodium thiosulphate) is an inorganic compound with the formula Na 2 S 2 O 3 ·(H 2 O) x. Typically it is available as the white or colorless pentahydrate (x = 5), which is a white solid that dissolves well in water. The compound is a reducing agent and a ligand, and these properties underpin its applications. [2]
Thiosulfate (IUPAC-recommended spelling; sometimes thiosulphate in British English) is an oxyanion of sulfur with the chemical formula S 2 O 2− 3.Thiosulfate also refers to the compounds containing this anion, which are the salts of thiosulfuric acid, such as sodium thiosulfate Na 2 S 2 O 3 and ammonium thiosulfate (NH 4) 2 S 2 O 3.
The first patent for an oxygen scavenger used an alkaline solution of pyrogallic acid in an air-tight vessel. [7] [8] Modern scavenger sachets use a mixture of iron powder and sodium chloride. [8] Often activated carbon is also included as it adsorbs some other gases and many organic molecules, further preserving products and removing odors.
Sulfites used in food processing (but not as a preservative) are required to be listed if they are not incidental additives (21 CFR 101.100(a)(3)), and if there are more than 10 ppm in the finished product (21 CFR 101.100(a)(4)) On July 8, 1986, sodium bisulfite (and other sulfites : "The chemicals affected by the order are sulfur dioxide ...
Antichlors include sodium bisulfite, potassium bisulfite, sodium metabisulfite, sodium thiosulfate, and hydrogen peroxide. [1] [2] [3] In the textile industry, the antichlor is usually added right before the end of the bleaching process. Antichlors are used mainly on fiber, textiles, and paper pulp.
The evidence for sodium thiosulfate's use is based on animal studies and case reports: the small quantities of cyanide present in dietary sources and in cigarette smoke are normally metabolized to relatively harmless thiocyanate by the mitochondrial enzyme rhodanese (thiosulfate cyanide sulfurtransferase), which uses thiosulfate as a substrate ...
Sodium tetrathionate is formed by the oxidation of sodium thiosulfate (Na 2 S 2 O 3), e.g. by the action of iodine: [1] 2 Na 2 S 2 O 3 + I 2 → Na 2 S 4 O 6 + 2 NaI. The reaction is signaled by the decoloration of iodine. This reaction is the basis of iodometric titrations. Other methods include the coupling of sodium bisulfite with disulfur ...
Thioglycolic acid is prepared by reaction of sodium or potassium chloroacetate with alkali metal hydrosulfide in aqueous medium. [19] It can be also prepared via the Bunte salt obtained by reaction of sodium thiosulfate with chloroacetic acid: [7] [20] ClCH 2 CO 2 H + Na 2 S 2 O 3 → Na[O 3 S 2 CH 2 CO 2 H] + NaCl Na[O 3 S 2 CH 2 CO 2 H] + H 2 ...