Chem Lab Worx
Compound profile · Acrylics

2-Hydroxyethyl Methacrylate (HEMA)

2-Hydroxyethyl methacrylate

The functional monomer that puts hydroxyl groups on acrylic resins, turning them into polyols that crosslink with isocyanates.

CAS868-77-9
FormulaC₆H₁₀O₃
Function–OH site

What it is

2-Hydroxyethyl methacrylate is a methacrylate ester carrying a primary hydroxyl group (molecular weight about 130.1 g/mol). It is a clear liquid miscible with water and many solvents.

Role in coatings

HEMA is copolymerized into acrylic polyols for 2K polyurethane topcoats and clearcoats, and into some latex and UV-cure resins to add adhesion and crosslinking sites. The amount used sets the polyol’s hydroxyl content and crosslink density.

Chemistry & key properties

Its methacrylate double bond polymerizes into the acrylic backbone, leaving the –OH group pendant. Those hydroxyls react with isocyanate hardeners to form urethane crosslinks, or with melamine resins in baked finishes.

Handling & storage

HEMA is a well-documented skin sensitizer and allergic contact dermatitis is common with uncured (meth)acrylates. Avoid all skin contact and use suitable gloves, since some glove materials are quickly permeated by acrylates.

Safety noteSummary information only. Always read the supplier’s Safety Data Sheet for the specific grade you use and follow local regulations.
FAQ

Common questions

Why does HEMA matter for urethane topcoats?

It supplies the hydroxyl groups on acrylic polyols that react with HDI or IPDI hardeners, forming the crosslinked network of a 2K acrylic urethane.

Is cured HEMA a sensitizer?

The concern is mainly uncured monomer. Fully cured polymers contain very little free monomer, but raw material handling requires strict skin protection.

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