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246794

Sigma-Aldrich

Pentaerythritol tetraacrylate, Pentaerythritol triacrylate, and Trimethylolpropane triacrylate mixture

Synonyme(s) :

PTA/TMPTA mixture, Pentaerythritol acrylates mixture

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About This Item

Numéro Beilstein :
6598752
Numéro CE :
222-540-8
Code UNSPSC :
12162002
ID de substance PubChem :
24854825
Nomenclature NACRES :
NA.23

Contient

300-400 ppm monomethyl ether hydroquinone as inhibitor

Indice de réfraction

n20/D 1.483

Densité

1.18 g/mL at 25 °C

Chaîne SMILES 

O=C(C=C)OCC(COC(C=C)=O)(COC(C=C)=O)COC(C=C)=O.OCC(COC(C=C)=O)(COC(C=C)=O)COC(C=C)=O.CCC(COC(C=C)=O)(COC(C=C)=O)COC(C=C)=O

Description générale

Pentaerythritol tetraacrylate, Pentaerythritoltriacrylate, and Trimethylolpropane triacrylate mixture is a combination of three acrylate monomers widely used for cross-linking. The Pentaerythritol-based acrylate mixtureoffers advantages such as improved mechanical strength, flexibility, chemical resistance, and UV-curing properties. It finds applications in industries such as automotive coatings, electronics, packaging, and 3D bioprinting.

Application

Pentaerythritol tetraacrylate, Pentaerythritol triacrylate, and Trimethylolpropane triacrylate mixture can be used:

  • As a cross-linking agent to synthesize biodegradable poly (1,3-trimethylene carbonate) (PTMC) networks with improved creep resistance and thermal stability. PMTC networks find application in the field of soft tissue engineering.
  • As a monomer precursor to prepare light-curing dental composites via photopolymerization.
  • To fabricate polymer-dispersed liquid crystal(PDLC) films with low driving voltage, moderately high contrast ratio, and fast response time. These PDLC films are utilized in optoelectronic devices such as OLEDs, FET, and solar cells.
  • As a monomer mixture to prepare 3D bioprinting resins viaphotopolymerization.

Pictogrammes

Health hazardExclamation markEnvironment
GHS08,GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H315,H317,H319,H351,H410

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

230.0 °F - closed cup

Point d'éclair (°C)

110 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificats d'analyse (COA)

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Biodegradable cross-linked poly (1, 3-trimethylene carbonate) networks formed by gamma irradiation under vacuum
Xiliang Liu, et al.
Polymers For Advanced Technologies, 32, 4373-4385 (2021)
Hui Huang et al.
Journal of chromatography. A, 1251, 82-90 (2012-07-06)
A mixed-mode monolithic stationary phase was prepared for capillary liquid chromatography (cLC) by in situ copolymerization of 4-vinylphenylboronic acid (VPBA) and pentaerythritol triacrylate (PETA) in a binary porogenic solvent consisting of ethylene glycol/cyclohexanol. The monomer of VPBA functioned as ion-exchange
Salvatore Surdo et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(14), 1900304-1900304 (2019-08-06)
Light interference is the primary enabler of a number of optical maskless techniques for the large-scale processing of materials at the nanoscale. However, methods controlling interference phenomena can be limited in speed, ease of implementation, or the selection of pattern
Xiaochun Wang et al.
Journal of chromatography. A, 1216(21), 4611-4617 (2009-04-04)
A polar and neutral polymethacrylate-based monolithic column was evaluated as a hydrophilic interaction capillary electrochromatography (HI-CEC) stationary phase with small polar-neutral or charged solutes. The polar sites on the surface of the monolithic solid phase responsible for hydrophilic interactions were
Mohammad Mahdi Moein
Talanta, 224, 121794-121794 (2021-01-01)
Since chiral recognition mechanism based on molecularly imprinted polymers immerged, it has assisted countless chemical and electrochemical analytical sample preparation techniques. It has done this by enhancing the enatioseparation abilities of these techniques. The preparation and optimization of chiral molecularly
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