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About This Item
Empirical Formula (Hill Notation):
C12H15N3O3
CAS Number:
Molecular Weight:
249.27
Beilstein:
225482
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Quality Level
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
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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - STOT RE 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
319.1 °F - closed cup
Flash Point(C)
159.5 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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