2-Isocyanatoethyl methacrylate
ALDRICH/477060 - contains ≤0.1% BHT as inhibitor, 98%
Synonym: 2-
CAS Number: 30674-80-7
Empirical Formula (Hill Notation): C7H9NO3
Molecular Weight: 155.15
EC Number: 250-284-7
MDL Number: MFCD00080536
Linear Formula: H2C=C(CH3)CO2CH2CH2NCO
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 477060-50ML
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 477060-5ML
| assay | 98% |
| bp | 211 °C (lit.) |
| contains | ≤0.1% BHT as inhibitor |
| density | 1.098 g/mL at 25 °C (lit.) |
| InChI | 1S/C7H9NO3/c1-6(2)7(10)11 |
| InChI key | RBQRWNWVPQDTJJ-UHFFFAOYSA |
| mp | −45 °C (lit.) |
| refractive index | n |
| SMILES string | CC(=C)C(=O)OCCN=C=O |
| storage temp. | 2-8°C |
| Application: | 2-Isocyanatoethyl methacrylate can be used as: • A reactive monomer in the synthesis of poly(methyl urethane) acrylate oligomer for UV-curable coatings. By incorporating urethane and acrylate groups into the polymer, it enables the polymer to be utilized in UV-curable coatings, inks, and adhesives. • An additive in propylene carbonate-based electrolyte to enhance its properties, such as viscosity, conductivity, and stability. This improves the overall performance of the electrolyte and the battery. • As a modifier in the copolymerization process to prepare a bioprosthetic heart valve, which is used in the application of transcatheter aortic valve replacement. • A latent cross-linker for adhesive resins and coatings. |
| General description: | 2-Isocyanatoethyl methacrylate, belongs to the class of monomers known as isocyanate monomers. The presence of the isocyanate functional group in 2-Isocyanatoethyl methacrylate makes it highly reactive. This reactivity allows it to undergo polymerization and form cross-linked networks for the development of polymers with improved mechanical strength, chemical resistance, and adhesion properties. It is also used as a crosslinker in the manufacture of many resins, in electrodeposition, and adhesives, and as a co-monomer in crosslinked polymer polyolstyrene-acrylic resin, which is used in construction products, such as ceramic tile adhesives, fillers, putties, and elastomeric roof coatings. |
| Packaging: | 5, 50 mL in glass bottle |
| Symbol |    GHS05,GHS06,GHS08 |
| Signal word | Danger |
| Hazard statements | H302 - H315 - H317 - H318 - H330 - H334 |
| Precautionary statements | P260 - P280 - P301 + P312 - P302 + P352 - P304 + P340 + P310 - P305 + P351 + P338 |
| Hazard Codes | T |
| Risk Statements | 22-23-36/37/38-42/43 |
| Safety Statements | 23-26-36/37-45 |
| RIDADR | UN 2206PSN1B 6.1 / PGIII |
| WGK Germany | WGK 3 |
| Flash Point(F) | 210.2 °F - closed cup |
| Flash Point(C) | 99 °C - closed cup |
| Purity | 98% |
| bp | 211 °C (lit.) |
| mp | −45 °C (lit.) |
| Density | 1.098 g/mL at 25 °C (lit.) |
| Refractive Index | n |
| Storage Temp. | 2-8°C |
| UNSPSC | 12162002 |