Skip to Content
Merck
All Photos(1)

Documents

246794

Sigma-Aldrich

Pentaerythritol tetraacrylate, Pentaerythritol triacrylate, and Trimethylolpropane triacrylate mixture

Synonym(s):

PTA/TMPTA mixture, Pentaerythritol acrylates mixture

Sign Into View Organizational & Contract Pricing


About This Item

Beilstein:
6598752
EC Number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

contains

300-400 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.483

density

1.18 g/mL at 25 °C

SMILES string

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

General description

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.

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Effects of multifunctional acrylates and thiols on the morphology and electro-optical properties of polymer-dispersed liquid crystal films
Mohsin Hassan Saeed, et al.
Emerging Liquid Crystal Technologies V, 48, 1457-1466 (2021)
Marc Hippler et al.
Nature communications, 10(1), 232-232 (2019-01-18)
Stimuli-responsive microstructures are critical to create adaptable systems in soft robotics and biosciences. For such applications, the materials must be compatible with aqueous environments and enable the manufacturing of three-dimensional structures. Poly(N-isopropylacrylamide) (pNIPAM) is a well-established polymer, exhibiting a substantial
Erhan Bat et al.
Biomacromolecules, 11(10), 2692-2699 (2010-09-16)
Biodegradable elastomeric poly(trimethylene carbonate) (PTMC) networks were efficiently formed by gamma irradiating the linear polymer in the presence of pentaerythritol triacrylate (PETA). The properties of networks formed upon irradiation of PTMC films containing (0, 1, 5 wt %) PETA as
Ming-Luan Chen et al.
Journal of chromatography. A, 1228, 183-192 (2011-08-06)
A novel poly(N-acryloyltris(hydroxymethyl)aminomethane-co-pentaerythritol triacrylate) (NAHAM-co-PETA) monolith was prepared in the 100 μm i.d. capillary and investigated for capillary liquid chromatography (cLC). The polymer monolith was synthesized by in situ polymerization of NAHAM and PETA in the presence of polyethylene glycol
Brent Vernon et al.
Journal of biomedical materials research. Part A, 64(3), 447-456 (2003-02-13)
A novel process for the preparation of water-borne biomaterials for hard tissue repair from injectable precursors is described, where the precursors form crosslinked materials in situ under physiological conditions. The precursors react by means of a Michael-type addition reaction that

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service