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Merck
CN

412090

Bisphenol A ethoxylate diacrylate

average Mn ~512, EO/phenol 2

Synonym(s):

Bis(4-acryloxypolyethoxyphenyl)propane, Bisphenol A polyethylene glycol diether diacrylate, Ethoxylated bisphenol A diacrylate

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About This Item

Linear Formula:
[H2C=CHCO2(CH2CH2O)nC6H4-4-]2C(CH3)2
CAS Number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
MDL number:
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InChI

1S/C15H16O2.C3H4O2.C2H6O2/c1-15(2,11-3-7-13(16)8-4-11)12-5-9-14(17)10-6-12;1-2-3(4)5;3-1-2-4/h3-10,16-17H,1-2H3;2H,1H2,(H,4,5);3-4H,1-2H2

InChI key

HGARWRTUWINPJC-UHFFFAOYSA-N

SMILES string

OCCO.OC(=O)C=C.CC(C)(c1ccc(O)cc1)c2ccc(O)cc2

form

viscous liquid

mol wt

average Mn ~512

contains

1,000 ppm monomethyl ether hydroquinone as inhibitor

composition

EO/phenol, 2

refractive index

n20/D 1.534

density

1.14 g/mL at 25 °C

Quality Level

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General description

Bisphenol A ethoxylate diacrylate (BAED) features two acrylate groups derived from bisphenol A, which enhance its reactivity and allows formation of high-performance epoxy resins via free radical polymerizaton. The presence of the bisphenol moiety contributes to exceptional thermal stability, making BAED suitable for high-performance applications.

Application

Bisphenol A ethoxylate diacrylate can be used:
  • As a cross linker to prepare quaternary gel electrolyte system for energy storage application via a photo-initiated phase separation process. BAED enhances ionic conductivity and thermal stability.
  • As a cross-linking agent in the formulation of dental sealants.
  • As a precursor to synthesize polymer nano coatings for flexible packaging.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup


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