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Boron Trifluoride Diethyl Ether CAS No. 109-63-7

Product NameBoron Trifluoride Diethyl EtherMultiple NamesBoron Trifluoride Ethyl Ether;Diethyl Ether

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Content

It is used as a catalyst for alkylation and condensation reactions in organic synthesis, as well as a basic raw material for producing boron-hydrogen high-energy fuel or extracting isotope boron, and as a curing agent for epoxy resin. Advantage of Boron Trifluoride Diethyl Ether CAS No. 109-63-7 A widely used complex. Application in catalyst industry Easy storage and stable performance.


NameBoron trifluoride diethyl etherate
SynonymsBoronfluoride3
bf3-ethercomplex
Boron fluoride etherate
Boron trifluoride etherate
Boron fluoride monoetherate
Boron trifluoride ethyl ether
Boron fluoride diethyl etherate
diethyl ether--boron trifluoride
Boron trifluoride diethyl etherate
Boron Trifluoride Ethyl Ether Complex
Boron(III) fluoride ethylether complex
Boron trifluoride diethyl ether complex
1'-oxybis[ethane]]-trifluoro[(beta-4)-boro
1'-oxybis[ethane]]-trifluoro[(beta-4)-boro
CAS109-63-7
EINECS203-689-8
InChIInChI:1S/C4H10BF3O/c1-3-9(4-2)5(6,7)8/h3-4H2,1-2H3
InChIKeyMZTVMRUDEFSYGQ-UHFFFAOYSA-N


Molecular FormulaC4H10BF3O
Molar Mass141.93
Density1.15g/mL(lit.)
Melting Point−58°C(lit.)
Boling Point126-129°C(lit.)
Flash Point118°F
Water SolubilityReacts
SolubilityMiscible with ether and alcohol.
Vapor Presure4.2 mm Hg ( 20 °C)
Vapor Density4.9 (vs air)
Appearanceliquid
Specific Gravity1.126 (20/4℃)
Colorbrown
Exposure LimitACGIH: TWA 0.1 ppm; Ceiling 0.7 ppm
Merck14,1350
BRN3909607
Storage ConditionStore below +30°C.
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
Sensitive7: reacts slowly with moisture/water
Explosive Limit5.1-18.2%(V)
Refractive Indexn20/D 1.344(lit.)
Physical and Chemical PropertiesColorless fuming liquid.
UseIt can be used as a common analytical reagent, and can also be used as a catalyst for alkylation and condensation reactions in organic synthesis.

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