Boron Trifluoride Diethyl Etherate CAS#109-63-7

Powerful Lewis Acid Catalytic Activity – Boron trifluoride is a strong catalyst for key organic reactions like polymerization, alkylation, isomerization, and hydrocarbon processing.

Highly Adaptable Through Complex Formation – It can pair up with oxygen- or nitrogen-containing compounds to form stable complexes, which lets you adjust its reactivity for different reactions.

Improved Handling and Stability – When you use it as a complex—like boron trifluoride etherate—it's much easier and safer to work with than the gas form.

Broad Compatibility with Organic Compounds – It forms complexes with ethers, amines, phenols, thioethers, and other derivatives, making it suitable for all kinds of organic synthesis work.

Product Details
Chemical Properties
Product Application

Products Description of Boron Trifluoride Diethyl Etherate CAS#109-63-7

Boron trifluoride is a key Lewis acid catalyst used in organic synthesis, especially in polymerization, hydrocarbonization, alkylation, and isomerization reactions. Since the gas form is tricky to handle, it's usually combined with polar oxygen- or nitrogen-containing compounds to make stable complexes that can be adjusted to fit different reaction needs. The most popular one is boron trifluoride etherate. It can also form complexes with thioethers, ketones, anisole, phenol, amines, and lots of their derivatives.

Boron Trifluoride Diethyl Etherate CAS#109-63-7

Boron trifluoride diethyl etherate Chemical Properties

Melting point −58 °C(lit.)
Boiling point 126-129 °C(lit.)
Density 1.15 g/mL(lit.)
Vapor density 4.9 (vs air)
Vapor pressure 4.2 mm Hg ( 20 °C)
Refractive index n20/D 1.344(lit.)
Fp 118 °F
Storage temp. Store below +30°C.
Solubility Miscible with ether and alcohol.
Form liquid
Specific Gravity1.126 (20/4℃)
Color brown
Explosive limit5.1-18.2%(V)
Water Solubility Reacts
Sensitive Moisture Sensitive
Hydrolytic Sensitivity7: reacts slowly with moisture/water
Merck 141,350
BRN 3909607
Exposure limitsACGIH: TWA 0.1 ppm; Ceiling 0.7 ppm
StabilityStable. Highly flammable. May form explosive peroxides in contact with air or oxygen. Reacts exothermically with water to form extremely flammable diethyl ether and toxic, corrosive boron trifluoride hydrates. Also incompatible with bases, amines, alkali metals.
InChIKeyMZTVMRUDEFSYGQ-UHFFFAOYSA-N
CAS DataBase Reference109-63-7(CAS DataBase Reference)
NIST Chemistry ReferenceBoron trifluoride etherate(109-63-7)
EPA Substance Registry SystemBoron, trifluoro[1,1'-oxybis[ethane]]-, (T-4)- (109-63-7)

Safety Information

Hazard Codes T,C
Risk Statements 10-14-20/22-35-48/23-34-14/15-23-22
Safety Statements 16-23-26-36/37/39-45-8-28A-43
RIDADR UN 2604 8/PG 1
WGK Germany 3
F 10
Autoignition Temperature185 °C DIN 51794
TSCA Yes
HazardClass 8
PackingGroup I
HS Code 29319090
Hazardous Substances Data109-63-7(Hazardous Substances Data)

Product Application of Boron Trifluoride Etherate CAS#109-63-7

This material is widely used as a catalyst for cationic polymerization and in making butadiene rubber and polyformaldehyde. It's also a key ingredient for boron–hydrogen high-energy fuels and for extracting boron isotopes. In chemical synthesis, it's a common catalyst, and it's also an important starting material for producing boron–hydrogen high-energy dyes and isolating the boron-10 isotope.

Boron Trifluoride Diethyl Etherate CAS#109-63-7