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408263

Sigma-Aldrich

Pentaerythritol tetraacrylate

contains 350 ppm monomethyl ether hydroquinone as inhibitor

Synonym(s):

2,2-Bis[[(1-oxo-2-propenyl)oxy]methyl]-1,3-propanediyl ester, Tetramethylolmethane tetraacrylate

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About This Item

Linear Formula:
(H2C=CHCO2CH2)4C
CAS Number:
Molecular Weight:
352.34
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

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contains

350 ppm monomethyl ether hydroquinone as inhibitor

Quality Level

impurities

10-40% triester

refractive index

n20/D 1.487 (lit.)

density

1.19 g/mL at 25 °C (lit.)

SMILES string

C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C

InChI

1S/C17H20O8/c1-5-13(18)22-9-17(10-23-14(19)6-2,11-24-15(20)7-3)12-25-16(21)8-4/h5-8H,1-4,9-12H2

InChI key

KNSXNCFKSZZHEA-UHFFFAOYSA-N

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This Item
418749418730236241
contains

350 ppm monomethyl ether hydroquinone as inhibitor

contains

-

contains

-

contains

-

refractive index

n20/D 1.487 (lit.)

refractive index

n20/D 1.464

refractive index

n20/D 1.475

refractive index

-

impurities

10-40% triester

impurities

-

impurities

-

impurities

-

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

General description

Pentaerythritol tetraacrylate (PETA) is a hydrophobic tetrafunctional monomer that is majorly used as a crosslinking agent that facilitates an improvement in the surface morphology of the polymeric material. It can be synthesized by the suspension of pentaerythritol in the solution of triethylamine and dichloromethane. PETA can be used in coatings, adhesives, sealants, surface coating, and composites. Its reactivity and ability to form densely crosslinked networks make it an essential component in the formulation of UV-curable materials. PETA is also used as a key component in the preparation of biocompatible polypeptide-based interpenetrating network (IPN) hydrogels, which find applications in tissue engineering, drug delivery systems, or biomedical devices.[1][2][3]

Application

Pentaerythritol tetraacrylate can be used as a monomer:
  • To synthesize polymer electrolytes for the fabrication of lithium-sulfur batteries.
  • In the formulation of UV-curable epoxy acrylate coatings, to improve their mechanical properties and performance.
  • To prepare multifunctional silicone acrylate prepolymers for use in UV-curable coatings, to improve their mechanical and anti-oxygen inhibition properties.
  • In the UV-curable ink formulations.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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


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