Trimethyl bismuth

BiN3Si6C)8HS7, Silanamine, 1,1,1 -trimethyl-M-(thmethylsilyl)-, bismuth(3+) salt, [76505-24-3], 31 100... 

Other metal compounds that are capable of decomposing at end gas temperatures to produce oxide smokes also can act as anti-knocks. These include iron and nickel carbonyls, trimethyl bismuth and methyl cyclopen-tadienyl manganese tricarbonyl [6]. The last has been used commercially for some years in Canada. Its anti-knock properties also can be amplified by organic co-anti-knocks (diketones in this case) [47]. Concerns over the possible toxicity of fine aerosols which are emitted in the exhaust will limit the acceptability of these metal containing materials in the future. 

Trimethyl bismuth occurring in the environment was detected in several environmental sources [27]. Biomethylation of bismuth very likely involves non oxidative methyl transfer, suggesting that 2 c is the most likely methyl source. 

Dimethylhydroxybismuthine, (CH3)26iOH.—When trimethyl-bismuthine (2 mols.) and bismuth bromide (1 mol.) are allowed to react m ether solution, an oil is produced, which yields the hydroxide when treated with water. The compound is not stable when dry, and with hydrochloric acid it reacts as follows —... 

Benzyl trimethyl ammonium chioride Bismuth, subsalicylate trans-1,2-Bis (n-propylsulfonyl) ethene Bromine p-Chioroaniiine 4-Chloronitrobenzene Chlorophene Climbazole Dibutyl adipate 4,6-Dinitro-o-s-butylphenol ammonium salt 1,4-Dioxane Fenarimol Glyceryl-o-monochlorohydrin ... 

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