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Merck
CN

411736

1,6-Hexanediol dimethacrylate

contains 75.0-125.0 hydroquinone as inhibitor

Synonym(s):

1,6-Hexamethylene dimethacrylate, 1,6-Hexanediyl dimethacrylate

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About This Item

Linear Formula:
[H2C=C(CH3)CO2(CH2)3-]2
CAS Number:
6606-59-3
Molecular Weight:
254.32
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24865760
EC Number:
229-551-7
Beilstein/REAXYS Number:
1957290
MDL number:
MFCD00015425

Key Documents

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InChI key

SAPGBCWOQLHKKZ-UHFFFAOYSA-N

InChI

1S/C14H22O4/c1-11(2)13(15)17-9-7-5-6-8-10-18-14(16)12(3)4/h1,3,5-10H2,2,4H3

SMILES string

CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C

vapor pressure

0.02 mmHg ( 100 °C)

assay

≥90%

form

liquid

contains

75.0-125.0 hydroquinone as inhibitor

Quality Level

100

bp

>315 °C (lit.)

density

0.995 g/mL at 25 °C (lit.)

Related Categories

General description

1,6-Hexanediol dimethacrylate is a compound that belongs to the class of methacrylate polymers, recognized for its versatile applications in various fields, including biomedicine and materials science. In the biomedical field, 1,6-Hexanediol dimethacrylate is primarily utilized in dental materials, adhesives, and coatings. In dental applications, it is commonly used as a crosslinking agent in dental composites and adhesives, enhancing the mechanical strength and durability of restorative materials. Additionally, its properties make it suitable for use in tissue engineering scaffolds and drug delivery systems, where it can facilitate controlled release and provide a supportive environment for cell growth due to its biocompatibility.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX9969
MKCW0775
MKCS0387
MKCM6868
MKCF5568

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C Park et al.
Dental materials : official publication of the Academy of Dental Materials, 14(6), 385-393 (1999-09-14)
To explore possible enhancement of the mechanical properties of resin composites by aligning the filler particles. The resin for the composites consisted of urethane dimethacrylate (UDMA) and 1,6-hexanediol dimethacrylate (HDDMA) mixed in the ratio of 90 to 10; the filler
M Yatabe et al.
Journal of oral rehabilitation, 28(2), 180-185 (2001-04-12)
The purpose of this study was to clarify the effect of the reducing agent on the oxygen-inhibited layer of the cross-linked reline material. A commercial autopolymerizing reline resin containing 1,6-hexanediol dimethacrylate as cross-linking agent and 1 wt.% sodium sulphite solution
V M Urban et al.
Biomedical chromatography : BMC, 20(4), 369-376 (2005-09-24)
Two high-performance liquid chromatographic methods for determination of residual monomer in dental acrylic resins are described. Monomers were detected by their UV absorbance at 230 nm, on a Nucleosil C18 (5 microm particle size, 100 A pore size, 15 x
Masao Hanabusa et al.
Dental materials : official publication of the Academy of Dental Materials, 27(8), 818-824 (2011-05-21)
A great challenge regarding the ease-of-use of composites involves the development of 'self-adhesive' composites that no longer require a separate adhesive to bond to tooth enamel/dentin. To characterize the interfacial ultra-structure of an experimental self-adhesive filling material bonded to enamel
L Giachetti et al.
Operative dentistry, 37(1), 28-36 (2011-09-29)
To evaluate the compatibility between aged siloranes and methacrylate-based composites by simulating a common repair-technique. Twenty substrates were constructed using silorane (Filtek Silorane, 3M ESPE) and methacrylate composites (Filtek Supreme XT, 3M ESPE). Substrates were aged in 0.9% NaCl solution
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