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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

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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
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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

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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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ9196
MKCP4045
MKCL2166
MKCJ2540
MKCH2052

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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.

Chuanglong He et al.
Journal of biomedical materials research. Part A, 99(4), 655-665 (2011-09-29)
The radiation crosslinked poly(L-lactide) (PLLA) electrospun nanofibers have been developed with improved thermal stability and mechanical properties. Trially isocyanurate (TAIC) were added into PLLA solution at different weight ratios (1, 3, and 5%) and electrospun into nanofibrous mats, the mats
Qingbing Zeng et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 789(2), 265-272 (2003-05-14)
Biocompatible affinity adsorbents prepared from macroporous glycidyl methacrylate-triallyl isocyanurate copolymer (GT) has been used for removing circulating immune complexes (CICs). In this work, adsorption of circulating immune complexes on GT-based affinity adsorbents has been studied by using batch and hemoperfusion
Wonsung Choi et al.
Scientific reports, 7(1), 12037-12037 (2017-09-22)
Lithium-metal-based batteries, owing to the extremely high specific energy, have been attracting intense interests as post-Li-ion batteries. However, their main drawback is that consumption/de-activation of lithium metal can be accelerated when O
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Global Trade Item Number

SKUGTIN
114235-100G04061838701862
114235-500G04061838251909