N-Benzylacrylamide

97%

Reagent Code: #218483
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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 primarily as a reactive monomer in polymer synthesis, enabling the creation of functional polymers with cross-linking capabilities. Its acrylamide group participates in free radical polymerization, while the benzyl group imparts hydrophobic character and stability. Commonly applied in the development of specialty coatings, adhesives, and hydrogels where tailored solubility and mechanical strength are required. Also serves as an intermediate in synthesizing pharmaceuticals and agrochemicals due to its ability to form stable amide bonds. Its reactivity allows for post-polymerization modifications, making it useful in research settings for designing stimuli-responsive materials.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿530.00
inventory 25g
10-20 days ฿2,580.00
inventory 100g
10-20 days ฿8,900.00
inventory 500g
10-20 days ฿44,090.00

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N-Benzylacrylamide
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Used primarily as a reactive monomer in polymer synthesis, enabling the creation of functional polymers with cross-linking capabilities. Its acrylamide group participates in free radical polymerization, while the benzyl group imparts hydrophobic character and stability. Commonly applied in the development of specialty coatings, adhesives, and hydrogels where tailored solubility and mechanical strength are required. Also serves as an intermediate in synthesizing pharmaceuticals and agrochemicals due to it

Used primarily as a reactive monomer in polymer synthesis, enabling the creation of functional polymers with cross-linking capabilities. Its acrylamide group participates in free radical polymerization, while the benzyl group imparts hydrophobic character and stability. Commonly applied in the development of specialty coatings, adhesives, and hydrogels where tailored solubility and mechanical strength are required. Also serves as an intermediate in synthesizing pharmaceuticals and agrochemicals due to its ability to form stable amide bonds. Its reactivity allows for post-polymerization modifications, making it useful in research settings for designing stimuli-responsive materials.

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