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808725

Sigma-Aldrich

1,10-Decanediol dimethacrylate

contains 4-Methoxyphenol as inhibitor

Synonym(s):

2-Propenoic acid, 2-methyl-1,1′-(1,10-decanediyl) ester, Decamethylene glycol dimethacrylate

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5 G
$284.00

$284.00

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5 G
$284.00

About This Item

Empirical Formula (Hill Notation):
C18H30O4
CAS Number:
6701-13-9
Molecular Weight:
310.43
EC Number:
229-745-1
MDL number:
MFCD00080452
UNSPSC Code:
12162002
PubChem Substance ID:
329769120
NACRES:
NA.23

$284.00

Available to ship onMay 02, 2025Details

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assay

97%

Quality Level

100

form

liquid

contains

4-Methoxyphenol as inhibitor

refractive index

n/D 1.462

density

0.968 g/mL at 25 °C

SMILES string

CC(=C)C(=O)OCCCCCCCCCCOC(=O)C(C)=C

InChI

1S/C18H30O4/c1-15(2)17(19)21-13-11-9-7-5-6-8-10-12-14-22-18(20)16(3)4/h1,3,5-14H2,2,4H3

InChI key

LRZPQLZONWIQOJ-UHFFFAOYSA-N

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Application

1,10-decamethylene glycol dimethacrylate is a monomer that can be used to make materials for use in dental applications.[1][2][3] It could be used to prepare camphorquinone/amine based adhesive.[4]

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW9619V
MKCH2409

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Irini D Sideridou et al.
Dental materials : official publication of the Academy of Dental Materials, 27(10), 1003-1010 (2011-07-26)
This work is concerned with the study of the sorption and desorption process of water, ethanol or ethanol/water solution 50% (v/v) or 75% (v/v) by the dental resins prepared by light curing of Bis-GMA, Bis-EMA, UDMA, TEGDMA or D₃MA. A
Evaluation of cell responses toward adhesives with different photoinitiating systems.
Van Landuyt, Kirsten L., et al.
Dental Materials : Official Publication of the Academy of Dental Materials, 31(8), 916-927 (2015)
New Photocleavable structures. Diacylgermane-based photoinitiators for visible light curing
Ganster B, et al.
Macromolecules, 41, 2394-2400 (2008)
Norbert Moszner et al.
Dental materials : official publication of the Academy of Dental Materials, 22(12), 1157-1162 (2006-01-03)
The objective of this study was to investigate the use of three new bis-(acrylamide)s as cross-linker in resin-based composite restoratives. Selected mechanical properties such as flexural strength and flexural modulus of model composites containing bis-(acrylamide)s were investigated and compared to

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