Diurethane dimethacrylate - CAS 103597-45-1
Catalog number: 103597-45-1
Category: Inhibitor
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C41H50N6O2
Molecular Weight:
658.87
COA:
Inquire
Targets:
Others
Description:
Bisoctrizole, a benzotriazole derivative, is a broad-spectrum ultraviolet radiation absorber, absorbing UVB as well as UVA ray. It could also reflect and scatter UV.
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Purity:
98%
Appearance:
Off-White Solid
Synonyms:
2,2'-METHYLENEBIS[6-(2H-BENZOTRIAZOL-2-YL)-4-(1,1,3,3-TETRAMETHYLBUTYL)PHENOL];2,2'-METHYLENEBIS[6-(BENZOTRIAZOL-2-YL)-4-TERT-OCTYLPHENOL];BIS[3-(BENZOTRIAZOL-2-YL)-2-HYDROXY-5-TERT-OCTYLPHENYL]METHANE;2,2-methylenebis(6-(2H-benzotriazol-2-yl) -4-(1,;Met
Solubility:
10 mM in DMSO
Storage:
-20ºC Freeze
MSDS:
Inquire
Application:
Bisoctrizole is a broad-spectrum ultraviolet radiation absorber, absorbing UVB as well as UVA ray.
Shelf Life:
As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly
Quantity:
Grams-Kilos
Density:
1.16 g/cm3
InChIKey:
ZRFPPIQVEQSFRV-UHFFFAOYSA-N
InChI:
InChI=1S/C41H50N6O2/c1-38(2,3)24-40(7,8)26-19-34(46-42-30-15-11-12-16-31(30)43-46)28(36(48)21-26)23-29-35(47-44-32-17-13-14-18-33(32)45-47)20-27(22-37(29)49)41(9,10)25-39(4,5)6/h11-22,48-49H,23-25H2,1-10H3
Canonical SMILES:
CC(C)(C)CC(C)(C)C1=CC(=C(C(=C1)O)CC2=C(C=C(C=C2O)C(C)(C)CC(C)(C)C)N3N=C4C=CC=CC4=N3)N5N=C6C=CC=CC6=N5
1.Resistance against bacterial leakage of four luting agents used for cementation of complete cast crowns.
Zmener O, Pameijer CH, Hernández S. Am J Dent. 2014 Feb;27(1):51-5.
PURPOSE: To assess the sealing properties of four luting materials used for cementation of full cast crowns.
2.Effect of methacrylic monomers on phagocytes reactive oxygen species: a possible BDDMA modulating action.
Nocca G1, Lupi A, De Santis F, Giardina B, De Palma F, Chimenti C, Gambarini G, De Sole P. Luminescence. 2008 Jan-Feb;23(1):54-7. doi: 10.1002/bio.1018.
In the last years the studies regarding the biocompatibility of dental materials investigate, in addition to the classic cytotoxic tests, the interactions between the materials and the host cells to better explain the causes of the adverse effects observed sometimes in the clinical practice. In the present study the ability of diurethane dimethacrylate (DUDMA) and 1,4-butanediol dimethacrylate (BDDMA) methacrylic monomers present in dental composite resins to alter the functionality of peripheral blood monocytes (PBMs) and polymorphonucleate cells (PMNs) was examined. These cells are involve in the biological response to materials and in the host ability to respond to bacteria. The results obtained suggest that the examined methacrylates induce a relevant decrease of PBMs oxidative burst whereas the basal ROS production is only slightly decreased. In PMNs DUDMA induces a decrease of both basal and stimulated ROS production. BDDMA, on the contrary, it does not alter total oxidative burst in presence of stimulus while induces a statistically significant decrease of basal ROS production.
3.Physical and chemical properties of an antimicrobial Bis-GMA free dental resin with quaternary ammonium dimethacrylate monomer.
Huang QT1, He JW2, Lin ZM3, Liu F4, Lassila LV5, Vallittu PK6. J Mech Behav Biomed Mater. 2016 Mar;56:68-76. doi: 10.1016/j.jmbbm.2015.10.028. Epub 2015 Nov 11.
The objective of this study was to evaluate the antibacterial activity, physicochemical properties of the quaternary ammonium dimethacrylate monomer N,N-bis[2-(3-(methacryloyloxy)propanamido)-ethyl]-N-methylhexadecyl ammonium bromide (IMQ-16) containing diurethane dimethacrylate (UDMA)/tricyclodecane dimethanol diacrylate (SR833s) resin system and compare with bisphenylglycidyl dimethacrylate (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA) resin system. It was hypothesized that the physical and chemical properties of the experimental polymers would be comparable with Bis-GMA/TEGDMA polymer and IMQ-16 monomer could endow the UDMA/SR833s resin with antibacterial activity. Double bond conversion (DC) was measured using Fourier transform infrared spectroscopy (FTIR). Mechanical properties including flexural strength (FS) and flexural modulus (FM) were measured by three-point bending test with bars of 2mm×2mm×25mm. Water sorption (WS) and solubility (WSL) were also investigated.
4.Investigations towards nano-hybrid resin-based composites.
Ilie N1, Rencz A, Hickel R. Clin Oral Investig. 2013 Jan;17(1):185-93. doi: 10.1007/s00784-012-0689-1. Epub 2012 Mar 6.
OBJECTIVE: Clinical data indicate an increased trend in material fracture as reason for failure in composite restorations, questioning whether modern resin-based composites (RBCs) are able to fulfil the rising aesthetical demands and to provide at the same time a sufficient mechanical stability also in larger cavities. Nano-hybrid RBCs are promoted as materials with improved mechanical properties. The aim of this study was to analyse differences in mechanical properties within and between modern flowable and non-flowable nano-hybrid and micro-hybrid RBCs by measuring mechanical properties at macro- and micro-scale.
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Chemical Structure

CAS 103597-45-1 Diurethane dimethacrylate

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