2-(((4-Vinylbenzyl)oxy)methyl)oxirane

95% mix TBC as stabilizer

Reagent Code: #245492
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CAS Number 113538-80-0

science Other reagents with same CAS 113538-80-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.24 g/mol
Formula C₁₂H₁₄O₂
badge Registry Numbers
MDL Number MFCD00674039
thermostat Physical Properties
Boiling Point 299.22 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 1.088 g/cm3 at 25 °C (lit.)
Storage 2-8°C, dry

description Product Description

Used primarily as a reactive diluent and crosslinking agent in epoxy resin systems. Enhances the mechanical properties and thermal stability of coatings, adhesives, and composites. Its vinyl and epoxy functional groups allow for dual-cure mechanisms through radical and cationic polymerization, making it suitable for UV-curable formulations. Commonly employed in electronics encapsulation, printing inks, and high-performance composite materials where improved toughness and adhesion are required. Also utilized in the synthesis of functional polymers and modified resins for specialty applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,420.00
inventory 1g
10-20 days ฿1,840.00
inventory 25g
10-20 days ฿22,450.00

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2-(((4-Vinylbenzyl)oxy)methyl)oxirane
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Used primarily as a reactive diluent and crosslinking agent in epoxy resin systems. Enhances the mechanical properties and thermal stability of coatings, adhesives, and composites. Its vinyl and epoxy functional groups allow for dual-cure mechanisms through radical and cationic polymerization, making it suitable for UV-curable formulations. Commonly employed in electronics encapsulation, printing inks, and high-performance composite materials where improved toughness and adhesion are required. Also utili

Used primarily as a reactive diluent and crosslinking agent in epoxy resin systems. Enhances the mechanical properties and thermal stability of coatings, adhesives, and composites. Its vinyl and epoxy functional groups allow for dual-cure mechanisms through radical and cationic polymerization, making it suitable for UV-curable formulations. Commonly employed in electronics encapsulation, printing inks, and high-performance composite materials where improved toughness and adhesion are required. Also utilized in the synthesis of functional polymers and modified resins for specialty applications.

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