6729-79-9

Basic information

• Product Name: 1,4-PHENYLENE DIACRYLATE
• Synonyms: P-PHENYLENE DIACRYLATE;1,4-PHENYLENE DIACRYLATE;HYDROQUINONE DIACRYLATE;Hydroquinone diacrylate (p-Phenylene diacrylate);1,4-Phenylene bisacrylate;Benzene-1,4-diol diacrylate;Bis(acrylic acid)p-phenylene ester;Bisacrylic acid benzene-1,4-diyl ester
• CAS NO: 6729-79-9
• Molecular Formula: C₁₂H₁₀O₄
• Molecular Weight: 218.21
• EINECS: 229-780-2
• Product Categories: monomer
• Mol File: 6729-79-9.mol
• Article Data: 5

Chemical Properties

• Melting Point: 88-89°C
• Boiling Point: 352.6°C at 760 mmHg
• Flash Point: 178.4°C
• Appearance: /
• Density: 1.161g/cm³
• Vapor Pressure: 3.81E-05mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: 1,4-PHENYLENE DIACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-PHENYLENE DIACRYLATE(6729-79-9)
• EPA Substance Registry System: 1,4-PHENYLENE DIACRYLATE(6729-79-9)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 6729-79-9(Hazardous Substances Data)

Usage

General Description

1,4-Phenylene diacrylate is a chemical compound commonly used in the production of various polymers and resins. It belongs to the group of diacrylate monomers, which are known for their use in the formulation of light-cured materials, adhesives, and coatings. Due to its high reactivity and ability to polymerize quickly when exposed to ultraviolet light, 1,4-phenylene diacrylate is widely used as a crosslinking agent in the manufacture of dental composites, optical adhesives, and other light-cured materials. It is also known for its exceptional adhesive properties and resistance to abrasion, making it a valuable component in the production of durable and high-performance polymer materials.

InChI:InChI=1/C12H10O4/c1-3-11(13)15-9-5-7-10(8-6-9)16-12(14)4-2/h3-8H,1-2H2

Upstream product

• 123-31-9 hydroquinone 
• 814-68-6 acryloyl chloride 
• 3233-36-1 p-hydroxyphenyl acrylate 
• 74-86-2 acetylene 

Downstream Products

• 86860-32-4 3-[1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-propionic acid 4-{3-[1-(3,4-dimethoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-propionyloxy}-phenyl ester 
• 86881-84-7 3-Diethylamino-propionic acid 4-(3-diethylamino-propionyloxy)-phenyl ester 
• 86860-37-9 1,4-bis-(3-dimethylaminopropionyloxy)benzene 

Relevant articles and documents

A facile approach to bis(Isoxazoles), promising ligands of the ampa receptor

A convenient synthetic approach to novel functionalized bis(isoxazoles), the promising bivalent ligands of the AMPA receptor, was elaborated. It was based on the heterocyclization reactions of readily available electrophilic alkenes with the tetranitromethane-triethylamine complex. The structural diversity of the synthesized compounds was demonstrated. In the electrophysi-ological experiments using the patch clamp technique on Purkinje neurons, the compound 1,4-phenylenedi(methylene)bis(5-aminoisoxazole-3-carboxylate) was shown to be highly potent positive modulator of the AMPA receptor, potentiating kainate-induced currents up to 70% at 10?11 M.

Synthesis and characterization of triptycene type cross-linker and its use in photoinduced curing applications

A novel triptycene type diacrylate cross-linker, triptycene hydroquinone diacrylate (THDA) was synthesized from the reaction of triptycene hydroquinone with acryloyl chloride and characterized. The photocuring behaviour and the reaction kinetics of the synthesized cross-linker were investigated by means of photo-differential scanning calorimetry (photo-DSC) experiments. Formulations containing monofunctional (meth)acrylate monomers, namely glycidyl methacrylate (GMA), 2-hydroxyethyl acrylate (HEA), 2-hydroxyethyl methacrylate (HEMA), and 2-ethylhexyl methacrylate (EHMA), cross-linker, THDA and 2,2-dimethoxy-2-phenylacetophenone (DMPA) as a photoinitiator were irradiated. A?conventional cross-linker without triptycene unit such as hydroquinone diacrylate (HDA) was used under the same conditions for comparison. The effects of the structure of the monofunctional monomer and triptycene moiety on the photopolymerization kinetics were evaluated and discussed.

Biodegradable neuromuscular blocking agents. Part V. α,ω-bisquaternary polyalkylene phenolic esters

A small group of α,ω-bisquaternary polyalkylene esters of quinol, catechol, and pyrogallol have been synthesised, and tested as potential biodegradable neuromuscular blocking agents. Three of the compounds were virtually inactive and the remainder of low potency compared to that of tubocuranine. Duration of action and vagal blockade have also been recorded.