2-Vinylpyridin-4-amine

≥95%

Reagent Code: #245470
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CAS Number 102000-57-7

science Other reagents with same CAS 102000-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 120.15 g/mol
Formula C₇H₈N₂
badge Registry Numbers
MDL Number MFCD11656644
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used primarily as a monomer in the synthesis of functional polymers, this compound contributes to the development of specialty resins with applications in coatings, adhesives, and ion-exchange materials. Its amine and vinyl groups enable cross-linking and copolymerization, enhancing the thermal and chemical resistance of resulting polymers. It is also explored in the preparation of adsorbent materials for metal ion recovery and in catalysis support due to its nitrogen-containing structure. Additionally, derivatives find use in pharmaceutical intermediates where nitrogen-rich heterocyclic systems are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿58,550.00
inventory 50mg
10-20 days ฿5,580.00
inventory 250mg
10-20 days ฿16,740.00

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2-Vinylpyridin-4-amine
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Used primarily as a monomer in the synthesis of functional polymers, this compound contributes to the development of specialty resins with applications in coatings, adhesives, and ion-exchange materials. Its amine and vinyl groups enable cross-linking and copolymerization, enhancing the thermal and chemical resistance of resulting polymers. It is also explored in the preparation of adsorbent materials for metal ion recovery and in catalysis support due to its nitrogen-containing structure. Additionally,

Used primarily as a monomer in the synthesis of functional polymers, this compound contributes to the development of specialty resins with applications in coatings, adhesives, and ion-exchange materials. Its amine and vinyl groups enable cross-linking and copolymerization, enhancing the thermal and chemical resistance of resulting polymers. It is also explored in the preparation of adsorbent materials for metal ion recovery and in catalysis support due to its nitrogen-containing structure. Additionally, derivatives find use in pharmaceutical intermediates where nitrogen-rich heterocyclic systems are required.

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