α-Vinylbenzyl alcohol

97%

Reagent Code: #245390
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CAS Number 42273-76-7

science Other reagents with same CAS 42273-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 134.18 g/mol
Formula C₉H₁₀O
badge Registry Numbers
MDL Number MFCD00093987
thermostat Physical Properties
Boiling Point 101-102 °C/12 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.021g/mL
Storage Room temperature, dry

description Product Description

Used as a reactive monomer in polymer synthesis, α-Vinylbenzyl alcohol contributes to the production of specialty resins and copolymers with enhanced adhesion and compatibility properties. Its hydroxyl and vinyl groups allow dual reactivity, making it valuable in crosslinking applications for coatings, adhesives, and sealants. It is also employed in modifying epoxy and acrylic systems to improve flexibility and cure response. Due to its ability to participate in free radical and cationic curing, it finds use in radiation-curable formulations such as UV-curable inks and coatings. Additionally, it serves as an intermediate in synthesizing esters and ethers for agrochemicals and pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿1,890.00
inventory 5g
10-20 days ฿12,450.00
inventory 1g
10-20 days ฿4,020.00

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α-Vinylbenzyl alcohol
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Used as a reactive monomer in polymer synthesis, α-Vinylbenzyl alcohol contributes to the production of specialty resins and copolymers with enhanced adhesion and compatibility properties. Its hydroxyl and vinyl groups allow dual reactivity, making it valuable in crosslinking applications for coatings, adhesives, and sealants. It is also employed in modifying epoxy and acrylic systems to improve flexibility and cure response. Due to its ability to participate in free radical and cationic curing, it finds

Used as a reactive monomer in polymer synthesis, α-Vinylbenzyl alcohol contributes to the production of specialty resins and copolymers with enhanced adhesion and compatibility properties. Its hydroxyl and vinyl groups allow dual reactivity, making it valuable in crosslinking applications for coatings, adhesives, and sealants. It is also employed in modifying epoxy and acrylic systems to improve flexibility and cure response. Due to its ability to participate in free radical and cationic curing, it finds use in radiation-curable formulations such as UV-curable inks and coatings. Additionally, it serves as an intermediate in synthesizing esters and ethers for agrochemicals and pharmaceuticals.

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