Boron Trifluoride Diethyl Etherate

1.Superior Lewis acid catalytic performance: Boron trifluoride delivers potent catalytic effects in critical organic reactions including polymerization, alkylation, isomerization, and hydrocarbon conversion processes.

2.Tunable reactivity via complexation: It is capable of forming stable complexes with oxygen or nitrogen containing compounds, enabling adjustment of its reactivity to match diverse reaction specifications.

3.Enhanced usability and stability: Complex forms such as boron trifluoride etherate offer far greater ease of operation and safety relative to its gaseous counterpart.

4.Excellent compatibility with organic substances: It readily complexes with ethers, amines, phenols, thioethers and other derivatives, suiting it for extensive use in organic synthesis.

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

Boron trifluoride functions as an essential Lewis acid catalyst for organic synthesis, extensively applied in reactions including polymerization, hydrocarbon conversion, alkylation and isomerization. Given the challenges in handling its gaseous state, it is frequently complexed with polar oxygen or nitrogen-bearing compounds to yield stable adducts tailored to varying reaction activity demands. Boron trifluoride etherate ranks among the most commonly utilized such complexes. Furthermore, boron trifluoride can form complexes with thioethers, ketones, anisole, phenol, amines and numerous related derivatives.

Boron Trifluoride Diethyl Etherate

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)

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

It is extensively adopted as a catalyst for cationic polymerization, as well as in the manufacturing of butadiene rubber and polyoxymethylene. Moreover, it acts as a critical feedstock for boron-hydrogen high-energy fuels and the separation of boron isotopes. Within chemical synthesis, it is frequently utilized as a catalyst, and also functions as a vital precursor for synthesizing boron-hydrogen high-energy materials and extracting boron-10 isotopes.

Boron Trifluoride Diethyl Etherate

Online Consultation

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