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Merck
CN

771562

Sigma-Aldrich

Tetraethylene glycol dimethacrylate

contains ≤1500 ppm MEHQ as inhibitor, 95%

Synonym(s):

PEG bismethacrylate, PEG dimethacrylate, PEG hydrogel

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About This Item

Linear Formula:
O[CH2CH2OCH2CH2OCOC(CH3)=CH2]2
CAS Number:
109-17-1
Molecular Weight:
330.37
Beilstein:
1803537
EC Number:
203-653-1
MDL number:
MFCD00014932
UNSPSC Code:
12162002
PubChem Substance ID:
329767504
NACRES:
NA.23

Key Documents

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Assay

95%

form

liquid

contains

≤1500 ppm MEHQ as inhibitor

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.465

density

1.082 g/mL at 20 °C (lit.)
1.089 g/mL at 25 °C

storage temp.

−20°C

SMILES string

C=C(C)C(OCCOCCOCCOCCOC(C(C)=C)=O)=O

InChI

1S/C16H26O7/c1-13(2)15(17)22-11-9-20-7-5-19-6-8-21-10-12-23-16(18)14(3)4/h1,3,5-12H2,2,4H3

InChI key

LTHJXDSHSVNJKG-UHFFFAOYSA-N

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Application

High purity PEG dimethacrylates are commonly used in PEG-based hydrogels and crosslinking hydrophilic polymers.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBP7506V

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Mariah S. Hahn
Material Matters, 5(3), 62-62 (2010)
Andrea Kasko
Material Matters, 6(3), 67-67 (2011)
Nívea Regina de Godoy Fróes-Salgado et al.
Odontology, 103(2), 160-168 (2014-04-15)
This study evaluated the effect of the combination of two dimethacrylate-based monomers [bisphenol A diglycidyl dimethacrylate (BisGMA) or bisphenol A ethoxylated dimethacrylate (BisEMA)] with diluents either derived from ethylene glycol dimethacrylate (ethylene glycol dimethacrylate, diethylene glycol dimethacrylate, triethylene glycol dimethacrylate
Jin-Oh You et al.
Biomaterials, 57, 22-32 (2015-05-10)
A principal challenge in wound healing is a lack of cell recruitment, cell infiltration, and vascularization, which occurs in the absence of temporal and spatial cues. We hypothesized that a scaffold that expands due to local changes in pH may
E A Dailing et al.
Journal of dental research, 93(12), 1326-1331 (2014-09-25)
Polymeric dental adhesives require the formation of densely crosslinked network structures to best ensure mechanical strength and durability in clinical service. Monomeric precursors to these materials typically consist of mixtures of hydrophilic and hydrophobic components that potentially undergo phase separation
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