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114235

Sigma-Aldrich

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

98%

Synonyme(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

Formule empirique (notation de Hill):
C12H15N3O3
Numéro CAS:
1025-15-6
Poids moléculaire :
249.27
Numéro Beilstein :
225482
Numéro CE :
213-834-7
Numéro MDL:
MFCD00006554
Code UNSPSC :
12162002
ID de substance PubChem :
24847161
Nomenclature NACRES :
NA.23

Niveau de qualité

200

Pureté

98%

Contient

500 ppm tert-butylhydroquinone as inhibitor

Indice de réfraction

n20/D 1.513 (lit.)

Point d'ébullition

149-152 °C/4 mmHg (lit.)

Densité

1.159 g/mL at 25 °C (lit.)

Chaîne SMILES 

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

Clé InChI

KOMNUTZXSVSERR-UHFFFAOYSA-N

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Description générale

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

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H373

Classification des risques

Acute Tox. 4 Oral - STOT RE 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

319.1 °F - closed cup

Point d'éclair (°C)

159.5 °C - closed cup

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number
MKCW4899
MKCR9213
MKCJ2540
MKCQ9196
MKCP4045

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Consulter la Bibliothèque de documents

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
Bolesław Szadkowski et al.
Materials (Basel, Switzerland), 13(3) (2020-02-06)
Perlite and vermiculite are naturally occurring minerals, commonly used by industry to obtain highly thermoisolative and/or non-flammable materials. However, there has been little research into the preparation and application of rubber compounds containing these inexpensive mineral fillers. Here, we show
Cheng-Lan Lin et al.
Journal of chromatography. A, 1272, 65-72 (2012-12-25)
This study describes the ability of triallyl isocyanurate (TAIC)-co-methacrylate ester polymer monoliths as stationary phases for the separation of hydrophilic compounds (phenolic acids, amino acids and catecholamines) in capillary electrochromatography (CEC) and ultra high pressure liquid chromatography (UHPLC). Several TAIC-co-methacrylate
Zhiquan Li et al.
Photochemistry and photobiology, 95(5), 1219-1229 (2019-03-19)
Designing digital light processing (DLP) 3D printable photosensitive resins with antibacterial properties is especially vital because of their potential applications in various biomedical fields. In this contribution, a thiol-ene-acrylate ternary system with reduced volume shrinkage and fast photopolymerization rate was
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
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