This information is only displayed if the substance is well-defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. EC Number 209-254-9. [7], Silver acetate is also a well known precursor used in printed electronics. Bull. Required fields are marked *. To install click the Add extension button. The ‘Substance identity’ section is calculated from substance identification information from all ECHA databases. Substances may have impurities and additives that lead to different classifications. The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. The Support section provides tools and practical guidance to companies which have responsibilities under the EU chemicals legislation. It is possible that a harmonisation is introduced through an amendment to the CLP Regulation. Oral administration is a relevant route ... A method to prepare (Z)-2-methylene-1-sulfonylindolin-3-ols efficiently that relies on silver acetate catalyzed hydroamination of 1-(2-(sulfonylamino)phenyl)prop-2-yn-1-ols is reported. In 1974, silver acetate was first introduced in Europe as an over-the-counter smoking-deterrent lozenge (Repaton) and then three years later as a chewing gum (Tabmint). Silver acetate Ag(OAc) NSC112212. What is the reflection of the story the mats by francisco arcellana? If at least one company has indicated that the substance classification is affected by impurities or additives, this will be indicated by an informative sentence. Substances for which classification and labelling data have been notified to ECHA by manufacturers or importers. [8], The LD50 of silver acetate in mice is 36.7 mg/kg. This information is only displayed if the substance is well–defined, its identity is not claimed confidential and there is sufficient information available in ECHA’s databases for ECHA’s algorithms to generate a molecular structure. More information about CAS and the CAS registry can be found here. Absorption Disposition Metabolism Elimination (Gavage) (K00073C) Completed . Acetic acid, silver(1+) salt (1:1) 19PPS85F9H. Silver acetate is an coordination compound with the empirical formula CH3CO2Ag (or AgC2H3O2). Please upgrade your Internet Explorer to a newer version. InfoCards are updated when new information is available. Acetic acid, silver(1+) salt; Silver(I) acetate; Silver monoacetate; Special Studies. It is the responsibility of the substance manufacturers and importers to consult official publications, e.g. The molecular formula identifies each type of element by its chemical symbol and identifies the number of atoms of each element found in one discrete molecule of the substance. Silver acetate is a reagent for direct ortho-arylation (to install two adjacent substituents on an aromatic ring) of benzylamines and N-methylbenzylamines. The structural formula of Silver Acetate is as shown below in the picture. Some substance identifiers may have been claimed confidential, or may not have been provided, and therefore not be displayed. Why is melted paraffin was allowed to drop a certain height and not just rub over the skin? We have created a browser extension. What is the Classification and Labelling Inventory? This site is not fully supported in Internet Explorer 7 (and earlier versions). 9 , CD000191, (2012). Download Product Safety Card; Recommended Products. It is a photosensitive, white, crystalline solid. 5, p. 932 - 934 Ag: MVol.B5, 2.2.1, page 121 - 122, Literature: Chemische Berichte, , vol. More information about Classification and Labelling is available in the Regulations section of ECHA website. Silver(1+) acetate. errors or omissions in the Database. Low doses of silver acetate in mice produced hyper-excitability, ataxia, central nervous system depression, labored breathing, and even death.

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