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Bismuth subsalicylate, sold generically as pink bismuth and under brand names including Pepto-Bismol, Pepti-Calm and BisBacter, is a medication used to treat temporary discomfort of the stomach and gastrointestinal tract. This includes an upset stomach, heartburn or other similar symptoms.
Bismuth is an ingredient in some pharmaceuticals, [9] although the use of some of these substances is declining. [56] Bismuth subsalicylate is used to treat diarrhea; [9] it is the active ingredient in such "pink bismuth" preparations as Pepto-Bismol, as well as the 2004 reformulation of Kaopectate.
2.2 A07BB Bismuth preparations. ... ATCvet codes without corresponding human ATC codes are cited with the leading Q in the following list.
Unlike the lighter pnictogens nitrogen, phosphorus, and arsenic, but similar to antimony, bismuth does not form a stable hydride. Bismuth hydride, bismuthine (BiH 3), is an endothermic compound that spontaneously decomposes at room temperature. It is stable only below −60 °C. [5] Bismuthides are intermetallic compounds between bismuth and ...
C05AX02 Bismuth preparations, combinations C05AX03 Other preparations, combinations C05AX04 Zinc preparations C05AX05 Tribenoside C05AX06 Phenylephrine.
Pages in category "Bismuth compounds" The following 53 pages are in this category, out of 53 total. This list may not reflect recent changes. A. Aurivillius phases; B.
Triphenylbismuth, an example of an organometallic bismuth(III) compound. Organobismuth chemistry is the chemistry of organometallic compounds containing a carbon to bismuth chemical bond. Applications are few. [1] [2] The main bismuth oxidation states are Bi(III) and Bi(V) as in all higher group 15 elements.
Preparation [ edit ] Dragendorff's reagent is prepared by mixing a concentrated solution of potassium iodide with a solution of bismuth subnitrate in a diluted acid ( acetic acid or tartaric acid , hydrochloric acid or sulfuric acid is rarely being used) as a low pH is mandatory for this reagent.