2-Aminoethyl methacrylate hydrochloride

90%

Reagent Code: #135581
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CAS Number 2420-94-2

science Other reagents with same CAS 2420-94-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.62 g/mol
Formula C₆H₁₁NO₂·HCl
badge Registry Numbers
MDL Number MFCD00078260
thermostat Physical Properties
Melting Point 102-110°C (Lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive monomer in polymer chemistry, this compound is valued for introducing amine functionality into copolymers due to its primary amine group and methacrylate moiety. It enables the creation of functional polymers for use in biomedical applications such as drug delivery systems, dental resins, and tissue engineering scaffolds. Its amine group allows for easy post-polymerization modification, including conjugation with biomolecules or dyes. Commonly employed in surface coatings and adhesives, it enhances adhesion to substrates by forming covalent bonds or electrostatic interactions. Also utilized in hydrogel formulations where biocompatibility and tunable crosslinking are required. The hydrochloride salt form improves solubility in aqueous systems, making it suitable for emulsion and solution polymerizations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿590.00
5g
10-20 days ฿2,480.00
25g
10-20 days ฿10,990.00
100g
10-20 days ฿26,500.00
2-Aminoethyl methacrylate hydrochloride
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Used primarily as a reactive monomer in polymer chemistry, this compound is valued for introducing amine functionality into copolymers due to its primary amine group and methacrylate moiety. It enables the creation of functional polymers for use in biomedical applications such as drug delivery systems, dental resins, and tissue engineering scaffolds. Its amine group allows for easy post-polymerization modification, including conjugation with biomolecules or dyes. Commonly employed in surface coatings and adhesives, it enhances adhesion to substrates by forming covalent bonds or electrostatic interactions. Also utilized in hydrogel formulations where biocompatibility and tunable crosslinking are required. The hydrochloride salt form improves solubility in aqueous systems, making it suitable for emulsion and solution polymerizations.
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