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409006

Sigma-Aldrich

Di(ethylenglycol)dimethacrylat

95%, cross-linking reagent polymerization reactions, methacrylate, 300 ppm monomethyl ether hydroquinone as inhibitor

Synonym(e):

2,2′-Oxybisethanol dimethacrylate, 2,2′-Oxydiethyl dimethacrylate, Diethylene glycol, dimethacrylate, Polyethylene glycol

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About This Item

Lineare Formel:
[H2C=C(CH3)CO2CH2CH2]2O
CAS-Nummer:
2358-84-1
Molekulargewicht:
242.27
EG-Nummer:
219-099-9
MDL-Nummer:
MFCD00014931
UNSPSC-Code:
12162002
PubChem Substanz-ID:
24865615
NACRES:
NA.23

product name

Di(ethylenglycol)dimethacrylat, 95%

Qualitätsniveau

200

Assay

95%

Form

liquid

Enthält

300 ppm monomethyl ether hydroquinone as inhibitor

Eignung der Reaktion

reagent type: cross-linking reagent
reaction type: Polymerization Reactions

Brechungsindex

n20/D 1.458 (lit.)

bp

134 °C/2 mmHg (lit.)

Dichte

1.082 g/mL at 25 °C (lit.)

Ω-Ende

methacrylate

α-Ende

methacrylate

Polymerarchitektur

shape: linear
functionality: homobifunctional

SMILES String

CC(=C)C(=O)OCCOCCOC(=O)C(C)=C

InChI

1S/C12H18O5/c1-9(2)11(13)16-7-5-15-6-8-17-12(14)10(3)4/h1,3,5-8H2,2,4H3

InChIKey

XFCMNSHQOZQILR-UHFFFAOYSA-N

Anwendung

  • Urethane dimethacrylate-based photopolymerizable resins for stereolithography 3D printing: A physicochemical characterisation and biocompatibility evaluation.: This study explores the use of urethane dimethacrylate-based resins in stereolithography 3D printing. It includes an in-depth physicochemical characterization and assesses the biocompatibility of the materials, highlighting their potential for medical and dental applications (Pitzanti G et al., 2024).

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCT3327
MKCS0539
MKCN9488
MKCK9887
MKCD7013

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Die Dokumentenbibliothek aufrufen

Y Takahashi et al.
Journal of dental research, 83(4), 302-306 (2004-03-27)
Ethyleneglycol dimethacrylate monomers have been previously reported to stimulate the growth of certain caries-associated bacteria on the basis of turbidity measurements. To elucidate the detail of this effect, we examined the influence of resin monomers on the growth of Streptococcus
K S Anseth et al.
Journal of dental research, 75(8), 1607-1612 (1996-08-01)
During the polymerization of multifunctional monomers for dental restorations, typical final double-bond conversions range from 55 to 75%. The low conversion results in a large amount of extractable monomer, reduced adhesion to the filler, and the potential for increased swelling.
Liang-Qia Guo et al.
Guang pu xue yu guang pu fen xi = Guang pu, 26(8), 1483-1486 (2006-10-25)
A pH sensitive polymer was prepared by copolymerization of methacrylic acid as monomer, diethylene glycol dimethacrylate as cross-linking reagent, heptane as porogen, and fluorescent dye eosin as indicator. The factors of influence on the preparation, and the character of the
Ahmad Joumaa et al.
Polymers, 12(5) (2020-05-16)
A latex of amphiphilic star polymer particles, functionalized in the hydrophobic core with nixantphos and containing P(MAA-co-PEOMA) linear chains in the hydrophilic shell (nixantphos-functionalized core-crosslinked micelles, or nixantphos@CCM), has been prepared in a one-pot three-step convergent synthesis using reversible addition-fragmentation
S Lu et al.
Journal of controlled release : official journal of the Controlled Release Society, 57(3), 291-300 (1999-01-23)
A novel approach to immobilize nonuniform initial drug concentration profiles in multilaminated matrix devices utilizing photopolymerization techniques is presented. Solution polymerization of 2-hydroxyethyl methacrylate (HEMA) and diethylene glycol dimethacrylate (DEGDMA) in the presence of a model compound, acid orange 8
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