16926-87-7

Basic information

• Product Name: 2-HYDROXY-3-PHENOXYPROPYL METHACRYLATE
• Synonyms: 3-PHENOXY-2-HYDROXYPROPYL METHACRYLATE;2-HYDROXY-3-PHENOXYPROPYL METHACRYLATE;2-methyl-2-propenoicaci2-hydroxy-3-phenoxypropylester;2-Propenoicacid,2-methyl-,2-hydroxy-3-phenoxypropylester;3-Phenoxy-2-hydroxypropyl methacryla;3-O-Phenylglycerol 1-methacrylate;Methacrylic acid 2-hydroxy-3-phenoxypropyl ester;Einecs 240-994-5
• CAS NO: 16926-87-7
• Molecular Formula: C₁₃H₁₆O₄
• Molecular Weight: 236.26
• EINECS: 240-994-5
• Product Categories: monomer
• Mol File: 16926-87-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 392°C at 760 mmHg
• Flash Point: 147.3°C
• Appearance: /
• Density: 1.131g/cm³
• Vapor Pressure: 7.58E-07mmHg at 25°C
• Refractive Index: 1.521
• PKA: 13.02±0.20(Predicted)
• CAS DataBase Reference: 2-HYDROXY-3-PHENOXYPROPYL METHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXY-3-PHENOXYPROPYL METHACRYLATE(16926-87-7)
• EPA Substance Registry System: 2-HYDROXY-3-PHENOXYPROPYL METHACRYLATE(16926-87-7)

Safety Data

• Hazardous Substances Data: 16926-87-7(Hazardous Substances Data)

Usage

General Description

2-Hydroxy-3-phenoxypropyl methacrylate is a chemical compound used in the production of various polymer-based materials such as adhesives, coatings, and sealants. It is a methacrylate monomer that contains a hydroxy and a phenoxy group. This chemical is known for its ability to improve the adhesion and durability of polymer coatings and is commonly used in the manufacturing of acrylic resins. It is also used as a reactive diluent in the production of epoxy resins and can be found in water-based coatings and adhesives due to its hydrophilic nature. Overall, 2-Hydroxy-3-phenoxypropyl methacrylate is a versatile chemical that plays a crucial role in enhancing the performance and properties of various polymer-based materials.

InChI:InChI=1/C13H16O4/c1-10(2)13(15)17-9-11(14)8-16-12-6-4-3-5-7-12/h3-7,11,14H,1,8-9H2,2H3

Upstream product

• 106-91-2 2,3-Epoxypropyl methacrylate 
• 139-02-6 sodium phenoxide 
• 79-41-4 poly(methacrylic acid) 
• 122-60-1 Phenyl glycidyl ether 
• 79-10-7 acrylic acid 

Relevant articles and documents

AROMATIC GLYCOL ETHERS AS WRITING MONOMERS IN HOLOGRAPHIC PHOTOPOLYMER FORMULATIONS

The invention relates to a photopolymer formulation comprising specific aromatic glycol ethers as writing monomers, matrix polymers and a photoinitiator. The invention further provides an unexposed holographic medium obtainable using an inventive photopolymer formulation, and an exposed holographic medium obtainable by exposing a hologram into an inventive unexposed holographic medium. The invention likewise provides a visual display comprising an inventive exposed holographic medium, for the use of an inventive exposed holographic medium for production of chip cards, identification documents, 3D images, product protection labels, labels, banknotes or holographic optical elements, and specific aromatic glycol ethers.

CARBAMATE-METHACRYLATE MONOMERS AND THEIR USE IN DENTAL APPLICATIONS

The present invention relates, generally, to monomers containing carbamate-methacrylates or derivatives of carbamate-methacrylates, processes for making the monomers, and compositions comprising the monomers. The present invention also relates to methods of using the monomers, such as in dental applications, and in particular, dental restorative resins.

Reactivity of some carboxylic acids in reactions with some epoxides in the presence chromium (III) ethanoate

Reactivities have been compared of acetic, acrylic, and methacrylic acid in reactions with epichlorohydrin, phenylglycidyl ether, glycidyl acetate, and glycidyl methacrylate carried in the presence of chromium (III) ethanoate. The acid reactivities changed differently with respect to the oxirane series. The effect of solvents on the reactions of acids with epichlorohydrin has also been observed.