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Safety Information

411736

Sigma-Aldrich

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
Beilstein:
1957290
EC Number:
229-551-7
MDL number:
MFCD00015425
UNSPSC Code:
12162002
PubChem Substance ID:
24865760
NACRES:
NA.23

vapor pressure

0.02 mmHg ( 100 °C)

Quality Level

100

Assay

≥90%

form

liquid

contains

75.0-125.0 hydroquinone as inhibitor

refractive index

n20/D 1.458 (lit.)

bp

>315 °C (lit.)

density

0.995 g/mL at 25 °C (lit.)

SMILES string

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

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

InChI key

SAPGBCWOQLHKKZ-UHFFFAOYSA-N

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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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

228.2 °F - closed cup

Flash Point(C)

109 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

411736-100ML:
411736-VAR:
411736-BULK:
411736-25ML:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW0775
MKCS0387
MKCM6868
MKCF5568
MKBZ8405V

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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
N M Mohsen et al.
Journal of oral rehabilitation, 22(3), 183-189 (1995-03-01)
The effect of silanation on the dispersion of quartz and zirconia-silica fillers by monomers used to formulate composites was studied. Sixteen silane coupling agents and three methods were used, and the amounts of the monomers needed to reach wet and
D R Williams et al.
Primary dental care : journal of the Faculty of General Dental Practitioners (UK), 8(4), 151-155 (2002-01-22)
The fit of the denture base to the alveolar ridge progressively declines with alveolar ridge resorption. Once a denture becomes ill-fitting there are two main treatment options: to construct a new denture or to restore the fit of the existing
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
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