16969-10-1

Basic information

• Product Name: 2-HYDROXY-3-PHENOXYPROPYL ACRYLATE
• Synonyms: 2-Propenoicacid,2-hydroxy-3-phenoxypropylester;2-HYDROXY-3-PHENOXYPROPYL ACRYLATE;3-PHENOXY-2-HYDROXYPROPYL ACRYLATE;2-Hydroxy-3-phenoxypropyl acrylate contains 250 ppm monomethyl ether hydroquinone as inhibitor;2-Hydroxy-3-phenoxypropyl Acrylate (stabilized with MEHQ)
• CAS NO: 16969-10-1
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.24
• EINECS: 241-045-8
• Product Categories: monomer;AcrylateCarbonyl Compounds;Acrylic Monomers;C12 to C63;Esters;Monomers;Acrylate;Acrylic Monomers;Building Blocks;C12 to C63;Carbonyl Compounds;Chemical Synthesis;Materials Science;Organic Building Blocks;Polymer Science
• Mol File: 16969-10-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 325.4 °C at 760 mmHg
• Flash Point: 192 °F
• Appearance: /
• Density: 1.16 g/mL at 25 °C(lit.)
• Vapor Pressure: 1.76E-06mmHg at 25°C
• Refractive Index: n20/D 1.528(lit.)
• PKA: 13.04±0.20(Predicted)
• Water Solubility: 5.3g/L at 20℃
• CAS DataBase Reference: 2-HYDROXY-3-PHENOXYPROPYL ACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXY-3-PHENOXYPROPYL ACRYLATE(16969-10-1)
• EPA Substance Registry System: 2-HYDROXY-3-PHENOXYPROPYL ACRYLATE(16969-10-1)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 16969-10-1(Hazardous Substances Data)

Usage

Uses

Polymeric membranes for controlled drug release systems may be prepared by the photosynthesis of 2-hydroxy-3-phenoxypropyl acrylate by UV radiation. Tthe product can be used as a curing agent during the fabrication of poly (phenylene ether)-based substrate materials.

InChI:InChI=1/C12H14O4/c1-2-12(14)16-9-10(13)8-15-11-6-4-3-5-7-11/h2-7,10,13H,1,8-9H2

Upstream product

• 122-60-1 Phenyl glycidyl ether 
• 79-10-7 acrylic acid 
• 108-95-2 phenol 

Downstream Products

• 109359-23-1 C₃₉H₅₀N₂O₁₀ 
• 94041-14-2 (+/-)-5-(phenoxymethyl)-3-phenyl-1,3-oxazolidine-2-thione 

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.

Epoxy-acrylic macromolecular compounds on the basis of phenol and para-alkyl substituted phenol

Some phenolic glycidyl ethers and suitable acrylic monomers on the basis of phenol and para-alkyl [-CH3, -C(CH3)3, -C9H19] substituted phenols were synthesized and characterized. The monomers were thermally polymerized in the presence of benzoyl peroxide. The polymerization reaction was studied by viscometry, as well as by curing process. The synthesized polymers degrade statistically by a radical mechanism. The apparent thermal stability is higher for para-tert-butylphenol epoxy-acrylic polymer and lower for phenol epoxy-acrylic polymer.