Silver acetate 563-63-3 High Purity
Product Name: | Silver acetate | ||||
Synonyms: | Silver acetate purum p.a., >=99.0% (T);Aceticacid, silver(1+) salt (1:1);Silver acetate 99.99% trace Metals basis;SILVER ACETATE REAGENTPLUS(TM) 99%;Silver acetate, 99.99% metals basis;SILVER ACETATE, REAGENTPLUS, 99%;Silveracetate,99%;silver acetate, anhydrous | ||||
CAS: | 563-63-3 | ||||
MF: | C2H3AgO2 | ||||
MW: | 166.91 | ||||
EINECS: | 209-254-9 | ||||
Product Categories: | Organic-metal salt;metal acetate salt;bc0001 | ||||
Mol File: | 563-63-3.mol | ||||
Uses | Oxidizing agent for use in liquid ammonia: Kline, Kershner, Inorg. Chem. 5, 932 (1966). | Uses | In the health field, silver acetate-containing products have been used in gum, spray, and lozenges to deter smokers from smoking. The silver in these products, when mixed with smoke, creates an unpleasant metallic taste in the smoker's mouth, thus deterring them from smoking. Lozenges containing 2.5 mg of silver acetate showed "modest efficacy" on 500 adult smokers tested over a three-month period. However, over a period of 12 months, prevention failed. In 1974, silver acetate was first introduced in Europe as an over-thecounter smoking-deterrent lozenge (Repaton) and then three years later as a chewing gum (Tabmint). | Uses | It is a reagent in the laboratory as a source of silver ions lacking an oxidizing anion. It is a reagent for direct ortho-arylation, and for conversion of organohalogen compounds into alcohols. Woodward cis-hydroxylation reaction employs silver acetate and iodine for selective conversin of alkenes into cis-diols. Silver acetate is the more preferred reagent for facile carbonylation of primary and secondary amines. It is also employed in the preparation of highly reflective, conductive silvered polymer films. |
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