Boron Trifluoride Diethyl Etherate CAS#109-63-7

Powerful Lewis acid catalytic activity:Boron trifluoride provides strong catalytic performance in key organic reactions such as polymerization, alkylation, isomerization, and hydrocarbon processing.

Highly adaptable through complex formation:It can be combined with oxygen- or nitrogen-containing compounds to form stable complexes, allowing its reactivity to be tailored to different reaction requirements.

Improved handling and stability:When converted into complexes such as boron trifluoride etherate, it becomes much easier and safer to use compared with the gaseous form.

Broad compatibility with organic compounds:It readily forms complexes with ethers, amines, phenols, thioethers, and other derivatives, making it suitable for a wide range of organic synthesis applications.

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

Boron trifluoride acts as an essential Lewis acid catalyst for organic synthesis, extensively facilitating polymerization, hydrocarbylation, alkylation, isomerization and other chemical transformations. Given the inconvenience of direct manipulation of its gaseous state, it is generally complexed with polar oxygen- or nitrogen-bearing compounds to generate stable adducts tailored to the catalytic activity demands of diverse reactions. Boron trifluoride etherate ranks among the most prevalently utilized complexes of this kind. Furthermore, boron trifluoride can form coordination complexes with thioethers, ketones, anisole, phenol, amines and a great many of their derivative compounds.

Factory Showcase

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

Inventory Display

Boron Trifluoride Diethyl Etherate CAS#109-63-7

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

It is extensively deployed as a catalyst for cationic polymerization and for the manufacturing of polybutadiene rubber and polyoxymethylene. Moreover, it acts as a fundamental feedstock for boron-hydrogen high-energy fuels and the separation of boron isotopes. Within chemical synthesis workflows, it functions as a routine catalytic agent; additionally, it serves as a critical precursor for synthesizing boron-hydrogen high-energy colorants and purifying boron-10 isotopes.

Transportation and Delivery

Boron Trifluoride Diethyl Etherate CAS#109-63-7

Online Consultation

Please fill out the form below and we will contact you as soon as possible