1709-71-3

Basic information

• Product Name: 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE
• Synonyms: 1-(ACRYLOYLOXY)-3-(METHACRYLOYLOXY)-2-PROPANOL;3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE;2-Propenoicacid,2-hydroxy-1,3-propanediylester;2-Propenoic acid, 2-methyl-, 2-hydroxy-3-(1-oxo-2-propenyl)oxypropyl ester;1-Acryloyloxy-2-hydroxy-3-methacryoyloxypropane;2-HYDROXY-3-ACRYLOXY PROPYL METHACRYLATE;2-HYDROXY-3-ACRYLOYLOXY PROPYL METHACRYLATE;1-(Acryloyloxy)-3-(methacryloyloxy)-2-propanol (stabilized with MEHQ)
• CAS NO: 1709-71-3
• Molecular Formula: C₁₀H₁₄O₅
• Molecular Weight: 214.22
• Product Categories: Diacrylates & Dimethacrylates;Functional Materials;Reagent for High-Performance Polymer Research;Acrylic Monomers;Monomers;Polyfunctional Acrylics
• Mol File: 1709-71-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 301.7°C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.14 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000101mmHg at 25°C
• Refractive Index: n20/D 1.473(lit.)
• Storage Temp.: 2-8°C
• PKA: 12.51±0.20(Predicted)
• Water Solubility: Insoluble in water
• CAS DataBase Reference: 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE(1709-71-3)
• EPA Substance Registry System: 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE(1709-71-3)

Safety Data

• Hazard Codes: Xi
• Statements: 38-41-43
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 1709-71-3(Hazardous Substances Data)

Usage

General Description

3-(Acryloyloxy)-2-hydroxypropyl methacrylate is a chemical compound that is used in various industrial applications, such as in the production of polymers and adhesives. It is a derivative of methacrylate, a type of acrylic resin, and contains both acrylate and methacrylate functional groups. The presence of the hydroxypropyl group gives the compound additional hydrophilic properties, making it useful for formulating hydrogels and other water-based materials. Its acryloyloxy group makes it suitable for polymerization reactions, allowing it to be incorporated into various polymer compositions. Overall, this chemical has versatile properties that make it valuable for a wide range of applications in industries such as coatings, textiles, and healthcare.

InChI:InChI=1/C10H14O5/c1-4-9(12)14-5-8(11)6-15-10(13)7(2)3/h4,8,11H,1-2,5-6H2,3H3

Upstream product

• 106-91-2 2,3-Epoxypropyl methacrylate 
• 79-10-7 acrylic acid 

Downstream Products

• 1096159-24-8 2-methylacrylic acid 2-hydroxy-3-[3-(2-methylaziridin-1-yl)propionyloxy]propyl ester 

Relevant articles and documents

A contains the amine structure light-cured monomer and its preparation method (by machine translation)

The invention discloses a containing amine structure photo-polymerization of the monomer, involves the high molecular material synthesis field, based on the existing light curing system to initiate the medicinal preparation is easy from solidifying the coating in question of the migration, it has the following chemical structural formula: The invention also discloses the above-mentioned optical polymerization monomer preparation method, comprises the following steps: (1) methyl glycidyl acrylate and acrylic acid in the catalyst and the polymerization inhibitor of reaction; (2) instillment zhongzhong amine; (3) the purification of the reaction product; the beneficial effect of the present invention is characterized in that: the reaction process is simple, easy to control the process conditions, severe corrosion structure introduced into the polymerization system, can obtain certain property of antioxidant polymerization, so as to obtain better surface curing performance, while avoiding the migration of small molecule compounds, to prevent adverse effects on the light curing system. (by machine translation)

METHOD FOR PRODUCING HYDROXYALKYL(METH)ACRYLATES

The present invention relates to a continuous process for preparing hydroxyalkyl (meth)acrylates, more particularly those hydroxyalkyl (meth)acrylates which have more than one (meth)acrylate group per molecule.

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.