Boron Trifluoride Diethyl Etherate CAS#109-63-7

Robust Lewis Acid Catalytic Activity:
Boron trifluoride exhibits exceptional catalytic efficiency in pivotal organic transformations, including polymerization, alkylation, isomerization, and hydrocarbon processing.

Versatile Complexation Capability:
It readily forms stable complexes with oxygen- or nitrogen-containing compounds, enabling the fine-tuning of its reactivity to align with specific reaction requirements.

Enhanced Handling & Stability:
When complexed (e.g., as boron trifluoride etherate), its handling becomes significantly more convenient and safer compared to its gaseous state.

Broad Organic Compatibility:
It easily forms adducts with ethers, amines, phenols, thioethers, and numerous other derivatives, making it a versatile component for a diverse array of organic synthesis processes.

Product Details

Boron trifluoride stands as a crucial Lewis acid catalyst in organic synthesis, playing a widespread role in various key reactions such as polymerization, hydrocarbonization, alkylation, and isomerization. Due to the challenges associated with handling its gaseous form, it is typically combined with polar oxygen- or nitrogen-containing compounds to form stable complexes—these complexes are designed to meet the specific activity demands of different reaction processes.
Among these complexes, boron trifluoride diethyl etherate is one of the most extensively utilized. Furthermore, boron trifluoride possesses the ability to form complexes with a range of substances, including thioethers, ketones, anisole, phenol, amines, and numerous derivatives of these compounds.

Boron Trifluoride Diethyl Etherate CAS#109-63-7

 

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

Boron trifluoride etherate is widely utilized as a cationic polymerization catalyst, and also serves as a catalyst in the production of butadiene rubber and polyformaldehyde. Additionally, it acts as a key raw material for boron-hydrogen high-energy fuels and the extraction of boron isotopes. In chemical synthesis processes, it is commonly employed as a catalyst, and it also plays an important role as a starting material for the production of boron-hydrogen high-energy dyes and the isolation of boron-10 isotopes.

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)

Boron trifluoride diethyl etherate Chemical PropertiesSafety 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
10
Autoignition Temperature185 °C DIN 51794
TSCA Yes
HazardClass 8
PackingGroup I
HS Code 29319090
Hazardous Substances Data109-63-7(Hazardous Substances Data)

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