Triethylborane

Clear colourless to light amber solution. Miscible with most organic solvents; immiscible with water.

Reagent in organic syntheses blocking agent and radical initiator.

It is used in mixtures with triethylaluminumas hypergolic igniters in rocket propulsionsystems.

Triethylborane reacted with 8-hydroxyquinoline to synthesize three 8--?hydroxyquinolato (q) boron compounds B(C2H5)?2q (1)?, BPh2q (2)?, and B(2-?naph)?2q (3).

The Journal of Organic Chemistry, 51, p. 427, 1986 DOI: 10.1021/jo00354a002

Flammable, dangerous fire risk, ignites spontaneously in air. Reacts violently with water and oxidizing materials. Toxic by inhalation, strong irritant.

Triethylboron is a toxic substance. The toxicsymptoms from chronic exposure to thiscompound are not reported. Skin contact canburn tissues.

Triethylborane is a pyrophoric substance, igniting spontaneously on exposure to air, chlorine, or bromine. Explosion may result when mixed with oxygen. Contact with ozone, peroxides and other oxidants can cause explosion. Its concentrated solutions can be pyrophoric. Flash point of 1 M solution in hexane is －23°C ( －9°F), while that in tetrahydrofuran is －17°C (1°F) (Aldrich 1996). It decomposes explosively when mixed with water.

Pyrophoric

Poison by ingestion and intraperitoneal routes. Mildly toxic by inhalation. Animal experiments show that the vapor is a poison which causes pulmonary irritation and convulsions. A very dangerous fire hazard by spontaneous chemical reaction with oxichzers. Spontaneously flammable in air. Explodes in oxygen atmospheres. Hypergolic reaction with triethylaluminum. Ignites on contact with chlorine, bromine, or other halogens. Will react with water or steam to produce toxic and flammable vapors. To fight fire, do NOT use halogenated extinguishing agents. When heated to decomposition or upon contact with air it emits toxic acrid smoke and irritating fumes. See also BORANES and BORON COMPOUNDS.

It distils at 56-57o/220mm. It can also be purified via its ammonia addition complex which is distilled in a high vacuum, decomposed with dry HCl, and the Et3B is distilled out. It is commercially available as a 15% solution in hexane or as 1M solution in hexane. [Brown J Am Chem Soc 67 376 1945, Bamford et al. J Chem Soc 471 1946, Lin et al. J Organomet Chem 312 277 1986, Beilstein 4 III 1957, 4 IV 4359.]