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Merck

114235

Sigma-Aldrich

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

98%

Synonim(y):

1,3,5-Triallyl-1,3,5-triazinane-2,4,6-trione, 1,3,5-tri-2-propen-1-ylo-1,3,5-triazyna-2,4,6(1H,3H,5H )-trion, 1,3,5-trializocyjanuran, Izocyjanuran trialilu, Kwas 1,3,5-trializocyjanurowy, Kwas 1,3,5-tris-2′-propenyloizocyjanurowy

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About This Item

Wzór empiryczny (zapis Hilla):
C12H15N3O3
Numer CAS:
Masa cząsteczkowa:
249.27
Beilstein:
225482
Numer WE:
Numer MDL:
Kod UNSPSC:
12162002
Identyfikator substancji w PubChem:
NACRES:
NA.23

Próba

98%

zawiera

500 ppm tert-butylhydroquinone as inhibitor

współczynnik refrakcji

n20/D 1.513 (lit.)

bp

149-152 °C/4 mmHg (lit.)

gęstość

1.159 g/mL at 25 °C (lit.)

ciąg 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

Klucz InChI

KOMNUTZXSVSERR-UHFFFAOYSA-N

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Opis ogólny

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.

Zastosowanie

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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Piktogramy

Health hazardExclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Acute Tox. 4 Oral - STOT RE 2

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

319.1 °F - closed cup

Temperatura zapłonu (°C)

159.5 °C - closed cup

Środki ochrony indywidualnej

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


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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
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
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

Produkty

The Progress in Development of Dental Restorative Materials

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