3,9-Divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane

98 %

Reagent Code: #170843
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CAS Number 78-19-3

science Other reagents with same CAS 78-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.24 g/mol
Formula C₁₁H₁₆O₄
badge Registry Numbers
MDL Number MFCD00006564
thermostat Physical Properties
Melting Point 43-46°C (Lit.)
Boiling Point 108-110°C 2mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.2510 g/cm3
Storage Room temperature, dry

description Product Description

Used primarily as a crosslinking agent in the production of specialty polymers and resins, this compound enhances thermal stability and mechanical strength in polymer networks. It is particularly effective in radiation-curable systems, including UV-curable coatings, inks, and adhesives, where it contributes to rapid curing and improved film hardness. Its spirocyclic structure provides rigidity, making it valuable in high-performance optical materials and protective coatings. Additionally, it finds use in the synthesis of functional monomers for dental composites and other biomedical materials due to its ability to form dense, durable networks.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 25g
10-20 days ฿490.00
inventory 100g
10-20 days ฿1,730.00
inventory 500g
10-20 days ฿7,260.00

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3,9-Divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane
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Used primarily as a crosslinking agent in the production of specialty polymers and resins, this compound enhances thermal stability and mechanical strength in polymer networks. It is particularly effective in radiation-curable systems, including UV-curable coatings, inks, and adhesives, where it contributes to rapid curing and improved film hardness. Its spirocyclic structure provides rigidity, making it valuable in high-performance optical materials and protective coatings. Additionally, it finds use in

Used primarily as a crosslinking agent in the production of specialty polymers and resins, this compound enhances thermal stability and mechanical strength in polymer networks. It is particularly effective in radiation-curable systems, including UV-curable coatings, inks, and adhesives, where it contributes to rapid curing and improved film hardness. Its spirocyclic structure provides rigidity, making it valuable in high-performance optical materials and protective coatings. Additionally, it finds use in the synthesis of functional monomers for dental composites and other biomedical materials due to its ability to form dense, durable networks.

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