N-(2-Propenyl)-N-tert-butylacrylamide

95%

Reagent Code: #215272
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CAS Number 116628-43-4

science Other reagents with same CAS 116628-43-4

blur_circular Chemical Specifications

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Weight 167.25 g/mol
Formula C₁₀H₁₇NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a reactive monomer in polymer synthesis, particularly in the development of functional polymers with stimuli-responsive properties. Its structure allows for copolymerization with other vinyl monomers, making it suitable for creating smart hydrogels and temperature-sensitive materials. Commonly applied in drug delivery systems and controlled release applications due to the thermal responsiveness of resulting polymers. Also utilized in surface coatings and adhesives where enhanced crosslinking and stability are required. Its allyl and acrylamide groups enable dual reactivity, supporting use in advanced material design and specialty resins.

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inventory 1g
10-20 days ฿35,000.00

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N-(2-Propenyl)-N-tert-butylacrylamide
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Used as a reactive monomer in polymer synthesis, particularly in the development of functional polymers with stimuli-responsive properties. Its structure allows for copolymerization with other vinyl monomers, making it suitable for creating smart hydrogels and temperature-sensitive materials. Commonly applied in drug delivery systems and controlled release applications due to the thermal responsiveness of resulting polymers. Also utilized in surface coatings and adhesives where enhanced crosslinking and

Used as a reactive monomer in polymer synthesis, particularly in the development of functional polymers with stimuli-responsive properties. Its structure allows for copolymerization with other vinyl monomers, making it suitable for creating smart hydrogels and temperature-sensitive materials. Commonly applied in drug delivery systems and controlled release applications due to the thermal responsiveness of resulting polymers. Also utilized in surface coatings and adhesives where enhanced crosslinking and stability are required. Its allyl and acrylamide groups enable dual reactivity, supporting use in advanced material design and specialty resins.

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