2-Propenamide, 2-methyl-N-(2-phenylethyl)-|

95%

Reagent Code: #226426
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CAS Number 37140-96-8

science Other reagents with same CAS 37140-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.2536 g/mol
Formula C₁₂H₁₅NO
badge Registry Numbers
MDL Number MFCD24550546
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive monomer in polymer synthesis, this compound contributes to the production of specialty adhesives and coatings with enhanced durability and thermal stability. Its acrylamide structure allows for free-radical polymerization, making it suitable for creating cross-linked polymers used in surface coatings, sealants, and binding agents. It is also employed in the development of functional polymers for controlled release systems and in modifying polymer surfaces for improved adhesion in composite materials. Due to the presence of a phenylethyl group, it imparts hydrophobic character and enhances compatibility with aromatic polymer matrices.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿8,800.00
inventory 5g
10-20 days ฿24,000.00
inventory 10g
10-20 days ฿44,000.00
inventory 25g
10-20 days ฿96,000.00

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2-Propenamide, 2-methyl-N-(2-phenylethyl)-|
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Used primarily as a reactive monomer in polymer synthesis, this compound contributes to the production of specialty adhesives and coatings with enhanced durability and thermal stability. Its acrylamide structure allows for free-radical polymerization, making it suitable for creating cross-linked polymers used in surface coatings, sealants, and binding agents. It is also employed in the development of functional polymers for controlled release systems and in modifying polymer surfaces for improved adhesio

Used primarily as a reactive monomer in polymer synthesis, this compound contributes to the production of specialty adhesives and coatings with enhanced durability and thermal stability. Its acrylamide structure allows for free-radical polymerization, making it suitable for creating cross-linked polymers used in surface coatings, sealants, and binding agents. It is also employed in the development of functional polymers for controlled release systems and in modifying polymer surfaces for improved adhesion in composite materials. Due to the presence of a phenylethyl group, it imparts hydrophobic character and enhances compatibility with aromatic polymer matrices.

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