Skip to Content
Merck

Key Documents

View All Documentation

114235

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione

98%

Synonym(s):

1,3,5-Tri-2-propen-1-yl-1,3,5-triazine-2,4,6(1H ,3H ,5H )-trione, 1,3,5-Triallyl-1,3,5-triazinane-2,4,6-trione, 1,3,5-Triallylisocyanurate, 1,3,5-Triallylisocyanuric acid, 1,3,5-Tris-2′-propenylisocyanuric acid, Triallyl isocyanurate

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C12H15N3O3
CAS Number:
1025-15-6
Molecular Weight:
249.27
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24847161
EC Number:
213-834-7
Beilstein/REAXYS Number:
225482
MDL number:
MFCD00006554
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

assay

98%

contains

500 ppm tert-butylhydroquinone as inhibitor

refractive index

n20/D 1.513 (lit.)

bp

149-152 °C/4 mmHg (lit.)

density

1.159 g/mL at 25 °C (lit.)

SMILES string

C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O

InChI

1S/C12H15N3O3/c1-4-7-13-10(16)14(8-5-2)12(18)15(9-6-3)11(13)17/h4-6H,1-3,7-9H2

InChI key

KOMNUTZXSVSERR-UHFFFAOYSA-N

General description

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione, also known as triallyl isocyanurate (TAIC), is a versatile monomer widely employed in polymer synthesis as a crosslinking agent or co-monomer. It is commonly used as a key component in various applications, including rubber and plastic industries, coatings, adhesives, elastomers, and in the development of dental restorative materials.

Application

1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione can be used as:
  • A crosslinking agent or additive in the synthesis of polylactic acid /flax composite materials to enhance their properties and performance under gamma irradiation.
  • A monomer in the synthesis of flexible ionogels with good mechanical properties via in situ thiol-ene photopolymerization with trimethylolpropane tris(3-mercaptopropionate). These ionogels further find applications in electrochemical capacitors.
  • A monomer in the fabrication of the shape memory polymer substrates.
The Progress in Development of Dental Restorative Materials

Still not finding the right product?

Explore all of our products under 1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

hcodes

H302,H373

Hazard Classifications

Acute Tox. 4 Oral - STOT RE 2

wgk

WGK 1

flash_point_f

319.1 °F - closed cup

flash_point_c

159.5 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Storage Class

10 - Combustible liquids

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

The Progress in Development of Dental Restorative Materials

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market.