TRIETHYL BORANE

PRODUCT IDENTIFICATION

CAS NO.

97-94-9

TRIETHYLBORANE

EINECS NO.

202-620-9

FORMULA

(C2H5)3B

MOL WT. 97.994
H.S. CODE  

TOXICITY

Oral rat LD50: 235 mg/kg
SYNONYMS TEB; Triethylboron; Triethylborine;
Triethylborane 1M solution in Tetrahydrofuran or in Hexane;

SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE  
MELTING POINT  
BOILING POINT 95 C
SPECIFIC GRAVITY

0.677

SOLUBILITY IN WATER Reacts
pH

 

VAPOR DENSITY  
AUTOIGNITION

 

NFPA RATINGS Health: 3; Flammability: 2; Reactivity: 2

REFRACTIVE INDEX

 

FLASH POINT

 

STABILITY Prolonged exposure to air may form unstable peroxides. Triethylborane is a spontaneously combustible burning with a green flame. The solutions in hexane or THF are not pyrophoric.The solutions wills not react readily with atmospheric water. Polymerization may occur in the presence of cationic initiators. It is explosive with potassium hydroxide, sodium hydroxide, and sodium tetrahydroaluminate since caustic alkalies deplete the inhibitor.

GENERAL DESCRIPTION AND APPLICATIONS

Borane (boron hydride): any binary compound of boron and hydrogen.  The term borane describe sometimes denote substances considered to be derivatives of the boron-hydrogen compounds, such as BCl3 and B10H12I2. Borane can be made from magnesium boride (MgB2) with the action of acid or can be prepared by the breaking apart of complex molecules into simpler products on heating in the presence of hydrogen. Boranes form interesting structures which cannot be described by the conventional two-electron covalent bond model. There are fewer electrons forming the chemical bonds than required in normal electron-pair bonds. An electron pair bonds both boron and the bridging hydrogen atom to create three atoms bond. There are two major general formula system; BnHn+4 (nidoboranes) and BnHn+6 (arachnoboranes). The simplest is diborane (B2H6), highly reactive gas; used as a rocket fuel and in hydroboration process to prepare organoboranes which have application as intermediates for organic synthesis. Boranes are all reactive and oxidize readily in air. There is a wide range of boranes with shapes ranging from delicate spiders' webs to untidy birds' nests. There is also a wide range of borane derivatives containing other atoms, such as carbon and phosphorus. Carborane is a class of stable cluster compounds containing carbon,  boron and hydrogen external to the framework of the cluster; with general formula C2BnHn+2. Carborane bonds are non-classical but have thermal stability and neutron capture ability, when containing the 10B isotope. A cluster compound is one with insufficient electrons to allow for classical two-center two-electron bonds between all adjacent atoms. Boranes including borane (BH3), borobutane (B4H10), and borodecane (B10H14) are used as fuels for air breathing engines and rockets as thery have higher calorific values than hydroborons fuels, once proposed as high-energy fuels for aircraft and missiles. Boranes are used in the synthesis of other organic boron compounds and metal borohydrides. They are used as chemo- or stereo-selective reductants. They convert aldehydes (chemoselective), ketones (stereoselective) to the corresponding alcohols in the manufacture of pharmaceuticals and other fine chemicals. They are used in the reductive alkylation of amines, novel metals and oximes. They are used as polymerization initiators (especially Trialkylboranes) for many monomers. They are used in extracting metals (Ag, Pd, Au, Ni). Applications include metal coatings, fogging agents in photographic emulsions, polymer additives and nitride-boron coatings.
SALES SPECIFICATION (1.0 m SOLUTION)

APPEARANCE

Clear liquid
CONTENT

15.0% min in Hexane or 14.0% min in Tetrahydrofuran

WATER

0.1% max

TRANSPORTATION
PACKING 60kgs in drum
HAZARD CLASS 4.3 (Packing Group: I)
UN NO. 3194
OTHER INFORMATION
Hazard Symbols: XI F C, Risk Phrases: 11-17-19-34-36/37, Safety Phrases: 16-33-36/37/39-43A-45