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Sigma-Aldrich

Bisphenol A ethoxylate dimethacrylate

average Mn ~1,700, EO/phenol 15, contains 200 ppm MEHQ as inhibitor

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Synonym(s):
2,2-Bis(4-methacryloxypolyethoxyphenyl)propane, Bisphenol A-ethylene oxide adduct dimethacrylate, Ethoxylated bisphenol A dimethacrylate
Linear Formula:
[H2C=C(CH3)CO2(CH2CH2O)nC6H4-4-]2C(CH3)2
CAS Number:
41637-38-1
MDL number:
MFCD03703564
UNSPSC Code:
12162002
PubChem Substance ID:
24869017
NACRES:
NA.23

mol wt

average Mn ~1,700

Quality Level

100

contains

200 ppm MEHQ as inhibitor
200 ppm monomethyl ether hydroquinone as inhibitor

composition

EO/phenol, 15

refractive index

n20/D 1.493

density

1.12 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

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

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

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General description

Bisphenol A ethoxylate dimethacrylate is an acrylic cross-linker widely used as a precursor to fabricate tissue-mimicking materials for 3D printing, cross-linked gel electrolytes, and to synthesize copolymers via the photopolymerization process.

Application

The Progress in Development of Dental Restorative Materials

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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A study of cross-linked PEO gel polymer electrolytes using bisphenol A ethoxylate diacrylate: ionic conductivity and mechanical properties
Yongku Kang, et al.
Journal of Power Sources, 119-121, 432-437 (2003)
3D printing of noncytotoxic high-resolution microchannels in Bisphenol-a ethoxylate dimethacrylate tissue-mimicking materials
Roger Domingo-Roca, et al.
3D printing and additive manufacturing (2022)
UV light copolymerization of dimethyl vinylphosphonate with bisphenol A ethoxylate dimethacrylate
Lavinia Macarie, et al.
Iranian Polymer Journal, 25, 437-442 (2016)
Sabine H Dickens et al.
Dental materials : official publication of the Academy of Dental Materials, 26(7), 675-681 (2010-04-07)
To establish the relationship of resin composition and resin hydrophilicity (indicated by solubility parameters and logP) to water sorption (WS), solubility, and degree of double bond conversion (DC) of resin mixtures designed for adhesive restoratives by varying the concentration of
M N Mandikos et al.
The Journal of prosthetic dentistry, 85(4), 386-395 (2001-04-25)
Various new, second-generation indirect composites have been developed with claimed advantages over existing tooth-colored restorative materials. To date, little independent research has been published on these materials, and the properties specified in the advertising materials are largely derived from in-house
View All Related Papers

Articles

The Progress in Development of Dental Restorative Materials

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market.

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