N-(3,4-Dihydroxyphenethyl)acrylamide

≥95.0%(T)(HPLC)

Reagent Code: #215112
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CAS Number 201610-44-8

science Other reagents with same CAS 201610-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.23 g/mol
Formula C₁₁H₁₃NO₃
badge Registry Numbers
MDL Number MFCD18816133
thermostat Physical Properties
Melting Point 103 °C
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used in the synthesis of functional polymers and hydrogels due to its catechol group and polymerizable acrylamide moiety. The catechol structure enables strong adhesion to various surfaces, including metals and oxides, making it suitable for bioadhesives and coating materials. It is also employed in biomedical applications such as tissue engineering and drug delivery systems, where its biocompatibility and ability to form cross-linked networks are advantageous. Additionally, it serves as a monomer in developing stimuli-responsive materials that react to pH, temperature, or metal ions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,890.00
inventory 1g
10-20 days ฿16,380.00
inventory 250mg
10-20 days ฿6,390.00

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N-(3,4-Dihydroxyphenethyl)acrylamide
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Used in the synthesis of functional polymers and hydrogels due to its catechol group and polymerizable acrylamide moiety. The catechol structure enables strong adhesion to various surfaces, including metals and oxides, making it suitable for bioadhesives and coating materials. It is also employed in biomedical applications such as tissue engineering and drug delivery systems, where its biocompatibility and ability to form cross-linked networks are advantageous. Additionally, it serves as a monomer in dev

Used in the synthesis of functional polymers and hydrogels due to its catechol group and polymerizable acrylamide moiety. The catechol structure enables strong adhesion to various surfaces, including metals and oxides, making it suitable for bioadhesives and coating materials. It is also employed in biomedical applications such as tissue engineering and drug delivery systems, where its biocompatibility and ability to form cross-linked networks are advantageous. Additionally, it serves as a monomer in developing stimuli-responsive materials that react to pH, temperature, or metal ions.

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