2-Aminoethylacrylatehydrochloride

Reagent Code: #139274
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CAS Number 4200-86-6

science Other reagents with same CAS 4200-86-6

blur_circular Chemical Specifications

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Weight 151.59 g/mol
Formula C₅H₁₀ClNO₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as a reactive monomer in polymer chemistry, this compound enables the introduction of amine functionality into copolymers, enhancing adhesion, crosslinking, and surface reactivity. It is especially valuable in developing functional coatings, adhesives, and specialty films where improved bonding to substrates like metals, glass, or plastics is required. Its amine and acrylate groups allow dual reactivity, making it useful in UV-curable systems and hydrogels. It also finds use in modifying resins for ink formulations and in the synthesis of ion-exchange materials. Due to its hydrophilic nature, it can improve the water dispersibility of polymers, beneficial in environmentally friendly coating systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,400.00

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2-Aminoethylacrylatehydrochloride
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Used primarily as a reactive monomer in polymer chemistry, this compound enables the introduction of amine functionality into copolymers, enhancing adhesion, crosslinking, and surface reactivity. It is especially valuable in developing functional coatings, adhesives, and specialty films where improved bonding to substrates like metals, glass, or plastics is required. Its amine and acrylate groups allow dual reactivity, making it useful in UV-curable systems and hydrogels. It also finds use in modifying r

Used primarily as a reactive monomer in polymer chemistry, this compound enables the introduction of amine functionality into copolymers, enhancing adhesion, crosslinking, and surface reactivity. It is especially valuable in developing functional coatings, adhesives, and specialty films where improved bonding to substrates like metals, glass, or plastics is required. Its amine and acrylate groups allow dual reactivity, making it useful in UV-curable systems and hydrogels. It also finds use in modifying resins for ink formulations and in the synthesis of ion-exchange materials. Due to its hydrophilic nature, it can improve the water dispersibility of polymers, beneficial in environmentally friendly coating systems.

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