N-Benzylacrylamide

99%

Reagent Code: #217539
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CAS Number 13304-62-6

science Other reagents with same CAS 13304-62-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.21 g/mol
Formula C₁₀H₁₁NO
badge Registry Numbers
MDL Number MFCD00015333
thermostat Physical Properties
Melting Point 59-62 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in polymer chemistry as a crosslinking agent to enhance mechanical and thermal stability of polymer networks. Commonly employed in the synthesis of hydrogels for biomedical applications such as drug delivery and tissue engineering. Acts as a reactive monomer in copolymerization processes to introduce functional benzyl groups, improving compatibility and adhesion in coatings and adhesives. Also utilized in the development of stimuli-responsive materials due to its ability to participate in controlled radical polymerization techniques.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿4,450.00
inventory 100g
10-20 days ฿13,500.00

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N-Benzylacrylamide
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Used in polymer chemistry as a crosslinking agent to enhance mechanical and thermal stability of polymer networks. Commonly employed in the synthesis of hydrogels for biomedical applications such as drug delivery and tissue engineering. Acts as a reactive monomer in copolymerization processes to introduce functional benzyl groups, improving compatibility and adhesion in coatings and adhesives. Also utilized in the development of stimuli-responsive materials due to its ability to participate in controlled

Used in polymer chemistry as a crosslinking agent to enhance mechanical and thermal stability of polymer networks. Commonly employed in the synthesis of hydrogels for biomedical applications such as drug delivery and tissue engineering. Acts as a reactive monomer in copolymerization processes to introduce functional benzyl groups, improving compatibility and adhesion in coatings and adhesives. Also utilized in the development of stimuli-responsive materials due to its ability to participate in controlled radical polymerization techniques.

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