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1,2,3-propanetriyl triacrylate, also known as triacrylate, is a versatile chemical compound commonly used in the production of polymers and adhesives. It is a clear, colorless liquid that is highly reactive and forms strong bonds when polymerized.

5459-38-1

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5459-38-1 Usage

Uses

Used in Polymer and Adhesive Production:
1,2,3-propanetriyl triacrylate is used as a crosslinking agent for the production of acrylic polymers, enhancing their strength and durability.
Used in UV Curable Coatings and Inks:
1,2,3-propanetriyl triacrylate is used as a component in UV curable coatings and inks, providing excellent adhesion and curing properties.
Used in Dental Materials:
1,2,3-propanetriyl triacrylate is used in the manufacturing of dental materials, such as fillings and crowns, due to its strong bonding properties and biocompatibility.
Used in Optical Lenses and Contact Lenses:
1,2,3-propanetriyl triacrylate is utilized in the production of optical lenses and contact lenses, taking advantage of its excellent optical properties and biocompatibility.
Overall, 1,2,3-propanetriyl triacrylate is a crucial chemical in the field of polymer and material science, with applications spanning various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5459-38-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5459-38:
(6*5)+(5*4)+(4*5)+(3*9)+(2*3)+(1*8)=111
111 % 10 = 1
So 5459-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O6/c1-4-10(13)16-7-9(18-12(15)6-3)8-17-11(14)5-2/h4-6,9H,1-3,7-8H2

5459-38-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-di(prop-2-enoyloxy)propyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 1,2,3-Propanetriyl triacrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5459-38-1 SDS

5459-38-1Downstream Products

5459-38-1Relevant academic research and scientific papers

Modified acrylate, preparation method thereof and application of modified acrylate in preparation of conductive adhesive

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Paragraph 0061-0066, (2019/11/28)

The invention discloses modified acrylate, a preparation method thereof and application of modified acrylate in preparation of a conductive adhesive. Hydroxyl groups in a polyol acrylate monomer is converted into alpha-H-containing acetal groups so as to obtain the modified acrylate. The modified acrylate obtained through reduction of hydroxyl groups has low viscosity, and can be effectively usedas a reactive diluent in a photo-cured coating formula, and since the modified acrylate contains the alpha-H-containing acetal groups which can promote photopolymerization activity, the photo-curing activity can be improved, so that photocrosslinking is promoted without addition of a hydrogenation donor assistant, and the problem of oxygen inhibition is avoided. When the modified acrylate is applied to preparation of a photo-cured composition, the prepared photo-cured composition has easy curing and fast surface drying; and the invention also provides a method for preparing the alpha-H-containing acetal groups through a reaction between enol ether and hydroxyl groups of the polyol acrylate monomer, and provides application of the modified acrylate in preparation of the photo-cured composition and the conductive adhesive of the photo-cured composition.

Multifunctional monomers based on vinyl sulfonates and vinyl sulfonamides for crosslinking thiol-Michael polymerizations: Monomer reactivity and mechanical behavior

Sinha, Jasmine,Podgórski, Maciej,Huang, Sijia,Bowman, Christopher N.

supporting information, p. 3034 - 3037 (2018/03/28)

Multifunctional vinyl sulfonates and vinyl sulfonamides were conveniently synthesized and assessed in thiol-Michael crosslinking polymerizations. The monomer reactivities, mechanical behavior and hydrolytic properties were analyzed and compared with those of analogous thiol-acrylate polymerizations. Materials with a broad range of mechanical properties and diverse hydrolytic stabilities were obtained.

PH-SENSITIVE NANOPARTICLES FOR DETECTING AND PREVENTING FOOD SPOILAGE

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Paragraph 0122; 0123, (2018/10/21)

Nanoparticles and compositions thereof are provided for detecting and/or preventing food spoilage. Methods of making the nanoparticles and compositions, and methods of using the nanoparticles and compositions, e.g. in food packaging, are also provided. The nanoparticles can have a hydrophobic core containing a hydrophobic active agent, e.g. a hydrophobic dye and/or an antimicrobial agent, for detecting and/or preventing food spoilage. The nanoparticles can also have a copolymer of a hydrophobic polymer repeat unit, e.g. styrene or lactic acid, and a pH responsive dendrimer repeat unit. The pH responsive dendrimer repeat unit can have a pH responsive amine core having a plurality of branched acrylate arms extending therefrom. The nanoparticles can be chemically stable at neutral pH, and then release the hydrophobic active agent at a pH range indicative of food spoilage. By releasing the hydrophobic dye and/or antimicrobial agent, the nanoparticles can detect and/or inhibit food spoilage.

Organic phosphaphenanthrene derivatives, and preparation method and application thereof

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Paragraph 0071; 0072; 0073, (2016/10/09)

The invention discloses organic phosphaphenanthrene derivatives, and a preparation method and application thereof. The structural formula of the organic phosphaphenanthrene derivatives is disclosed as Formula I, wherein the group disclosed as Formula II is from carboxylic acid derivatives or acyl chloride derivatives, the group A is from organic phosphaphenanthrene compounds, and the group A is connected with the group disclosed as Formula II through a P-C bond. The preparation method of the organic phosphaphenanthrene derivatives comprises the following steps: carrying out esterification reaction on glycerol and carboxylic acid derivatives or acyl chloride derivatives to obtain glycerol ester derivatives; and under the action of a catalyst, carrying out reaction on the glycerol ester derivatives and organic phosphaphenanthrene compounds. The organic phosphaphenanthrene derivatives can enhance the flame retardancy of the polymer, and can enhance the flame retardancy of the prepared material when being added as a functional aid for preparing high-polarity engineering plastics of PET (polyethylene terephthalate), PBT (polybutylene terephthalate) and other polyesters and PA6 (polyamide 6), PA66 (polyamide 66) and other polyamides.

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