N-(2-Hydroxyethyl)methacrylamide

98%

Reagent Code: #218409
fingerprint
CAS Number 5238-56-2

science Other reagents with same CAS 5238-56-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.16 g/mol
Formula C₆H₁₁NO₂
thermostat Physical Properties
Boiling Point 323.434 ºC at 760mmHg
inventory_2 Storage & Handling
Density 0.95 g/cm3
Storage Room temperature

description Product Description

Used as a reactive monomer in the synthesis of hydrophilic hydrogels and polymer networks due to its ability to form covalent bonds during polymerization. Commonly employed in biomedical applications such as contact lenses, drug delivery systems, and tissue engineering scaffolds because of its hydrophilic nature and biocompatibility. Its hydroxyl group allows for further chemical modification, enabling tailored polymer properties. Also utilized in copolymer formulations to enhance hydrophilicity, flexibility, and surface adhesion. May be incorporated into coatings and adhesives for improved durability and specific performance characteristics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿490.00
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿1,720.00
inventory 5g
10-20 days ฿5,210.00
inventory 25g
10-20 days ฿17,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(2-Hydroxyethyl)methacrylamide
No image available

Used as a reactive monomer in the synthesis of hydrophilic hydrogels and polymer networks due to its ability to form covalent bonds during polymerization. Commonly employed in biomedical applications such as contact lenses, drug delivery systems, and tissue engineering scaffolds because of its hydrophilic nature and biocompatibility. Its hydroxyl group allows for further chemical modification, enabling tailored polymer properties. Also utilized in copolymer formulations to enhance hydrophilicity, flexibi

Used as a reactive monomer in the synthesis of hydrophilic hydrogels and polymer networks due to its ability to form covalent bonds during polymerization. Commonly employed in biomedical applications such as contact lenses, drug delivery systems, and tissue engineering scaffolds because of its hydrophilic nature and biocompatibility. Its hydroxyl group allows for further chemical modification, enabling tailored polymer properties. Also utilized in copolymer formulations to enhance hydrophilicity, flexibility, and surface adhesion. May be incorporated into coatings and adhesives for improved durability and specific performance characteristics.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...