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Safety boron halides

SAFETY PROFILE A human poison by an unspecified route. Poison experimentally by inhalation. An eye, mucous membrane, and systemic irritant by inhalation. Mutation data reported. A common air contaminant. Difficult to ignite. Explosion hazard when exposed to flame or in a fire. NH3 + air in a fire can detonate. Potentially violent or explosive reactions on contact with interhalogens (e.g., bromine pentafluoride, chlorine trifluoride), 1,2-dichloroethane (with liquid NH3), boron halides, chloroformamideium nitrate, ethylene oxide (polymerization reaction), magnesium... [Pg.65]

SAFETY PROFILE A poison. Corrosive. A skin, eye, and mucous membrane irritant. Dangerous may explode when heated. This and other boron halides react with water or steam to produce toxic and corrosive fumes and may explode. Incompatible with K Na. When heated to decomposition it emits toxic fumes of Br . See also BORON COMPOUNDS and HYDROBROMIC ACID. [Pg.206]

One of the earliest methods for preparing aromatic boronic acids involved the reaction between diaryl mercury compounds and boron trichloride [198]. As organomer-curial compounds are to be avoided for safety and environmental reasons, this old method has remained unpopular. In this respect, trialkylaryl silanes and stannanes are more suitable and both can be transmetallated efficiently with a hard boron halide such as boron tribromide [199]. The apparent thermodynamic drive for this reaction is the higher stability of B-C and Si(Sn)-Br bonds of product compared to the respective B-Br and Si(Sn)-C bonds of substrates. Using this method, relatively simple arylboronic acids can be made following an aqueous acidic workup to hydrolyze the arylboron dibromide product [193]. For example, some boronic acids were synthesized more conveniently from the trimethylsilyl derivative than by a standard ortho-metallation procedure (entry 11, Table 1.3). [Pg.34]

The addition of a gas to a reaction mixture (commonly the hydrogen halides, fluorine, chlorine, phosgene, boron trifluoride, carbon dioxide, ammonia, gaseous unsaturated hydrocarbons, ethylene oxide) requires the provision of safety precautions which may not be immediately apparent. Some of these gases may be generated in situ (e.g. diborane in hydroboration reactions), some may be commercially available in cylinders, and some may be generated by chemical or other means (e.g. carbon dioxide, ozone). An individual description of the convenient sources of these gases will be found under Section 4.2. [Pg.83]

Oxidizer, Poison, Corrosive SAFETY PROFILE Poisonous and corrosive. Very reactive, a powerful oxidizer. Explosive or violent reaction with organic materials, water, acetone, ammonium halides, antimony, antimony trichloride oxide, arsenic, benzene, boron, bromine, carbon, carbon monoxide, carbon tetrachloride, carbon tetraiodide, chloromethane, cobalt, ether, halogens, iodine, powdered molybdenum, niobium, 2-pentanone, phosphoms, potassium hexachloroplatinate, pyridine, silicon, silicone grease, sulfur, tantalum, tin dichloride, titanium, toluene, vanadium, uranium, uranium hexafluoride. [Pg.211]


See other pages where Safety boron halides is mentioned: [Pg.114]    [Pg.72]    [Pg.493]    [Pg.210]    [Pg.549]    [Pg.827]    [Pg.1060]    [Pg.98]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.5 , Pg.5 , Pg.5 ]




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