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Merck

436909

Diurethane dimethacrylate, mixture of isomers

contains 225 ppm±25 ppm BHT as inhibitor, ≥97%

동의어(들):

Di-HEMA trimethylhexyl dicarbamate, Diurethane dimethacrylate, Urethane dimethacrylate, methacrylate adduct

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
R'CH2[C(CH3)(R)CH2]2CH2R', R=H or CH3, R'=NHCO2CH2CH2O2CC(CH3)=CH2
CAS 번호:
Molecular Weight:
470.56
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
EC Number:
276-957-5
NACRES:
NA.23
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Quality Level

assay

≥97%

form

liquid

contains

225 ppm±25 ppm BHT as inhibitor

refractive index

n20/D 1.485 (lit.)

bp

200 °C (lit.)

density

1.11 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(CCNC(=O)OCCOC(=O)C(C)=C)CC(C)(C)CNC(=O)OCCOC(=O)C(C)=C

InChI

1S/C23H38N2O8/c1-16(2)19(26)30-10-12-32-21(28)24-9-8-18(5)14-23(6,7)15-25-22(29)33-13-11-31-20(27)17(3)4/h18H,1,3,8-15H2,2,4-7H3,(H,24,28)(H,25,29)

InChI key

UEKHZPDUBLCUHN-UHFFFAOYSA-N

General description

Diurethane dimethacrylate (DUDA) is a mixture of isomers that belongs to the class of methacrylate monomers. It is a bifunctional monomer, which contains two methacrylate groups and two urethane linkages. It is commonly used in the field of polymer chemistry as a crosslinking agent or a reactive diluent in adhesive materials, coatings, and composites. It has good mechanical and adhesive properties, which makes it suitable for various polymer applications.

Application

Diurethane dimethacrylate can be used as:
  • A monomer in the synthesis of the shape memory polymer that is used as the matrix material for the preparation of high-strength and stiffness composites. These composites show excellent shape memory behavior and mechanical strength, making them suitable for bone fixation devices.
  • A crosslinking agent to prepare the denture biomaterials, which contain antifungal drugs incorporated into the polymer matrix for controlling drug delivery.
  • A crosslinking agent in the synthesis of anion exchange membranes (AEMs) for use in electrochemical devices.
Diurethane dimethacrylate has been used as a precursor to fabricate the multifunctional polymer nanocomposite with enhanced luminescence activity. It can also be used in digital light processing (DLP) mediated 3D printing.


pictograms

Exclamation mark

signalword

Warning

hcodes

저장 등급

10 - Combustible liquids

flash_point_f

>212.0 °F

flash_point_c

> 100 °C

ppe

Eyeshields, Gloves

Hazard Classifications

Aquatic Chronic 3 - Skin Sens. 1B



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문서

Discover hydrogels, biocompatible materials for drug delivery, tissue engineering, wound care, and 3D bioprinting in innovative biomedical applications

Composite materials based on methacrylate monomers are used to provide aesthetic and functional restoration of dental tissue. Polymerization chemistries are being developed to improve the reliability of these materials.


Gaute Floer Johnsen et al.
Journal of dentistry, 56, 84-98 (2016-11-12)
This study aims at evaluating and comparing mechanical, chemical, and cytotoxicological parameters of a commercial brand name composite material against two 'own brand label' (OBL) composites. Parameters included depth of cure, flexural strength, degree of conversion, polymerization shrinkage, filler particle
Mehwish Pasha et al.
Materials science & engineering. C, Materials for biological applications, 114, 111040-111040 (2020-10-01)
Secondary caries is one of the most major cause for re-placement of dental composite restorations. Targeting the survival of cariogenic bacteria residing on the restoration surface may reduce this problem. The present study aims to evaluate the antibacterial potential as
Kyungsun Kim et al.
Materials (Basel, Switzerland), 14(4) (2021-03-07)
Concerns regarding unbound monomers in dental composites have increased with the increased usage of these materials. This study assessed the biological effects of urethane dimethacrylate (UDMA), a common monomer component of dental composite resins, on the cariogenic properties of Streptococcus