Description
4-(6-Methacryloyloxyhexyloxy)phenol (CAS No. 142627-92-7) is a high-purity specialty monomer designed for advanced polymer and material science applications. With the molecular formula C16H22O4 and IUPAC name 6-(4-hydroxyphenoxy)hexyl 2-methylprop-2-enoate, this compound features a reactive methacrylate group and a phenolic hydroxyl group, making it ideal for copolymerization and functionalization. Its extended hexyloxy spacer enhances flexibility and compatibility in polymer matrices. Suitable for photoresists, dental materials, and biocompatible coatings, this monomer is rigorously tested for consistency and performance. Packaged under inert conditions to ensure stability, it is a critical building block for researchers developing tailored polymeric materials.
Properties
- CAS Number: 142627-92-7
- Complexity: 293
- IUPAC Name: 6-(4-hydroxyphenoxy)hexyl 2-methylprop-2-enoate
- InChI: InChI=1S/C16H22O4/c1-13(2)16(18)20-12-6-4-3-5-11-19-15-9-7-14(17)8-10-15/h7-10,17H,1,3-6,11-12H2,2H3
- InChI Key: FPIGGWXEVBMWPF-UHFFFAOYSA-N
- Exact Mass: 278.15180918
- Molecular Formula: C16H22O4
- Molecular Weight: 278.34
- SMILES: CC(=C)C(=O)OCCCCCCOC1=CC=C(C=C1)O
- Topological: 55.8
- Monoisotopic Mass: 278.15180918
- Synonyms: SCHEMBL11172057, 4-(6-methacryloyloxyhexyloxy)phenol, 142627-92-7
Application
4-(6-Methacryloyloxyhexyloxy)phenol is widely used in polymer chemistry for synthesizing functionalized resins, photopolymers, and dental composites. Its dual reactivity enables crosslinking and post-modification in coatings and adhesives. Researchers leverage its phenolic group for antioxidant or UV-stabilizing properties in advanced material formulations. The monomer is also valuable in biomedical applications, such as drug delivery systems and biocompatible scaffolds.
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