N-(4-Acetylphenyl)acrylamide

98%

Reagent Code: #215068
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CAS Number 22535-53-1

science Other reagents with same CAS 22535-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD12091311
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used in polymer chemistry as a reactive monomer for synthesizing functional polymers with temperature or pH-responsive behavior. Its acrylamide group enables free-radical polymerization, making it suitable for creating copolymers in stimuli-responsive hydrogels and drug delivery systems. The ketone group in the structure allows for post-polymerization modifications via conjugation reactions, useful in bioconjugation and labeling applications. Also investigated as a building block in the development of specialty coatings and adhesives where tunable polarity and hydrogen bonding are required. Shows potential in textile and fiber treatments due to its ability to enhance binding and durability through covalent attachment to surfaces.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,500.00
inventory 1g
10-20 days ฿44,550.00
inventory 5g
10-20 days ฿155,930.00

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N-(4-Acetylphenyl)acrylamide
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Used in polymer chemistry as a reactive monomer for synthesizing functional polymers with temperature or pH-responsive behavior. Its acrylamide group enables free-radical polymerization, making it suitable for creating copolymers in stimuli-responsive hydrogels and drug delivery systems. The ketone group in the structure allows for post-polymerization modifications via conjugation reactions, useful in bioconjugation and labeling applications. Also investigated as a building block in the development of sp

Used in polymer chemistry as a reactive monomer for synthesizing functional polymers with temperature or pH-responsive behavior. Its acrylamide group enables free-radical polymerization, making it suitable for creating copolymers in stimuli-responsive hydrogels and drug delivery systems. The ketone group in the structure allows for post-polymerization modifications via conjugation reactions, useful in bioconjugation and labeling applications. Also investigated as a building block in the development of specialty coatings and adhesives where tunable polarity and hydrogen bonding are required. Shows potential in textile and fiber treatments due to its ability to enhance binding and durability through covalent attachment to surfaces.

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