Boron Trifluoride Dibutyl Etherate

GTC-250

Boron Compounds

Boron Trifluoride Dibutyl Etherate

CAS No.
593-04-4
Catalogue ID
GTC-250

Boron Trifluoride Dibutyl Etherate, CAS 593-04-4. Source-derived identification, physical data and applications are provided for catalogue reference; request the current specification, COA and SDS for the required grade.

Catalogue aliases / related identifiers

(Dibutyl ether)trifluoroboron; Trifluoroborane dibutyl etherate; Dibutyl ether-boron trifluoride; Boron trifluoride-dibutyl ether adduct; BF3-Dibutyl Etherate; Boron, (dibutyl ether)trifluoro-, (T-4)-

Supplied catalogue source: GTC-250 · Page 87

Reference data — confirm before ordering or use

The information below is a structured migration from the supplied catalogue snapshot. It is not a current product specification, COA or SDS. Confirm the actual supplier, grade, batch documents, classification, packing and destination requirements for your enquiry.


Basic Information of Boron Trifluoride Dibutyl Etherate

Boron Trifluoride Dibutyl Etherate (CAS No. 593-04-4) is characterized by the following properties:

CAS No.:593-04-4
EC No.:209-783-5
Linear Formula:C₈H₁₈BF₃O
Molecular Weight:198.03
Appearance:Pale yellow to brown liquid
Density:0.959 g/mL at 25 °C(lit.)
SolubilitySoluble in many organic solvents; reacts with water and protic solvents.
Flash Point:70 °C
Nature:Strong Lewis acid.
RIDADR:UN 2922 or UN 3264 8(6.1)/PG 2(3)
Chemical Structure:Molecular Structure of Boron Trifluoride Dibutyl Etherate

These attributes make it a preferred catalyst in processes requiring efficient and controlled Lewis acid activity.


Main Functions and Applications of Boron Trifluoride Dibutyl Etherate

  1. Synthesis of Polyformaldehyde Resin: Boron trifluoride dibutyl etherate is widely employed as a highly effective catalyst for the synthesis of polyformaldehyde resin, also known as polyoxymethylene (POM). It drives the cationic polymerization of formaldehyde or its cyclic oligomers (like trioxane) to produce this important engineering plastic.

  2. Preparation of Ethylene-Oxygen Methylene Copolymer: This complex also plays a crucial role as a catalyst in the preparation of ethylene-oxygen methylene copolymers, and more broadly, in the cationic ring-opening polymerization of cyclic ethers like ethylene oxide. These copolymers find applications in various specialty polymers and materials.


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Hazards Classification

  • GHS Classification: Acute Toxicity (GHS06), Corrosive (GHS05), Flammable Liquid (GHS02)

  • Hazard Statements: Toxic if swallowed, in contact with skin or if inhaled; Causes severe skin burns and eye damage; Combustible liquid.

  • UN Number: UN 2922 or UN 3264

  • Hazard Class: 8 (Corrosive Substances)

  • Subsidiary Hazard Class (for UN 2922): 6.1 (Toxic Substances)

  • Packing Group: II or III

GHS06: Acute toxicity pictogram
GHS06: Acute toxicity
GHS05: Corrosive pictogram
GHS05: Corrosive
GHS02: flammable pictogram
GHS02: Flammable



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