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

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

Uses

Used in Polymer and Adhesive Production:
3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE is used as a key component in the production of polymers and adhesives for its ability to enhance the properties of these materials, such as adhesion, flexibility, and durability.
Used in Coatings Industry:
In the coatings industry, 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE is used as a binder or additive to improve the performance characteristics of coatings, such as water resistance, adhesion, and durability.
Used in Textile Industry:
3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE is used as a finishing agent in textiles to provide properties like water resistance, softness, and improved durability to fabrics.
Used in Healthcare Industry:
In healthcare, 3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE is used as a component in the formulation of hydrogels and other biomaterials for medical applications, such as drug delivery systems and tissue engineering, due to its biocompatibility and hydrophilic nature.
Used in Hydrogel Formulation:
3-(ACRYLOYLOXY)-2-HYDROXYPROPYL METHACRYLATE is used as a monomer in the formulation of hydrogels for its ability to form stable, water-absorbing networks that can be tailored for specific applications, such as wound dressings or contact lenses.

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)

A dental repair material for methyl acrylate monomer and its preparation method

The invention discloses a dental repair material for methyl acrylate monomer, involves the high molecular material synthesis field, based on the existing light curing system for use in the medicinal preparation is easy from the amine helps initiate curing system in question of the migration, it has the following Chemical structural formula: The invention also discloses the preparation method of the monomer, comprising the following steps: (1) weighing methyl glycidyl acrylate and acrylic acid, the reaction is carried out to add catalyst and polymerization inhibitor; (2) to the reaction system to continue the reaction drop [...] compound; (3) after the reaction, reaction product to washing and drying; the beneficial effect of the present invention is characterized in that the: effective to avoid amine migration, thus prevent from dental repair material migrate in the precipitation, affect the applicability of the dental restoration material.

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.

Process for preparing hydroxyalkyl(meth) acrylates using Lewis acid catalysts

The present invention relates to a process for preparing hydroxyalkyl (meth)acrylates by reacting at least one compound A which contains at least one epoxide group with at least one compound B which contains at least one carboxylic acid group, wherein A and/or B also contains at least one (meth)acrylate group, in the presence of Lewis acid catalysts, each of which contains at least one directly bonded di(cyclo)alkylamino group.

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.