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Triallyl Isocyanurate - 98%,contains 500 ppm tert-butylhydroquinone as inhibitor, high purity , CAS No.1025-15-6

52 Citations COA COA
    Grade & Purity:
  • ≥98%
  • contains 500 ppm BHT as stabilizer
In stock
Item Number
T123406
Grouped product items
SKU Size
Availability
 Price Qty
T123406-25g
25g
≥10
$20.90
T123406-100g
100g
≥10
$41.90
T123406-500g
500g
3
$115.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Aromatic heterocyclic compounds (462) Divinyl monomer (31) Halogen free heterocyclic block (1207)

Basic Description

Synonyms 1,3,5-Triallylisocyanurate | 1,3,5-Tri-2-propenyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione | 1,3,5-Triallyl-1,3,5-triazinane-2,4,6-trione | TAIC | Isocyanuric acid triallyl ester | 1,3,5-Triallyl isocyanurate
Specifications & Purity ≥98%, contains 500 ppm BHT as stabilizer
Storage Temp Store at 2-8°C,Protected from light
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

The Progress in Development of Dental Restorative Materials

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Triazines
Subclass Triazinones
Intermediate Tree Nodes Not available
Direct Parent Triazinones
Alternative Parents 1,3,5-triazines  Heteroaromatic compounds  Ureas  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Triazinone - 1,3,5-triazine - Heteroaromatic compound - Urea - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as triazinones. These are compounds containing a triazine ring which bears a ketone group a carbon atom.
External Descriptors Not available

Associated Targets(Human)

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A498 (42825 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHN (49357 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CCRF-CEM (65223 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
COLO 205 (50209 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DLD-1 (17511 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DMS-273 (14108 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HL-60 (67320 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
K562 (73714 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KM12 (47707 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
M14 (47487 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MOLT-4 (49676 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OVCAR-3 (48710 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OVCAR-5 (45555 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OVCAR-8 (47708 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RPMI-8226 (44974 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RXF 393 (41971 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SF-295 (48000 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SK-MEL-5 (47095 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SK-OV-3 (52876 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SN12C (47755 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SNB-19 (46794 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SNB-78 (14240 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TK-10 (45540 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
U-251 (51189 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UACC-257 (46019 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UACC-62 (47335 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UO-31 (46270 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
786-0 (47912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
A549 (127892 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EKVX (44102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NCI-H322M (45589 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HCC 2998 (41480 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HCT-116 (91556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HOP-18 (11577 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HOP-92 (41141 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NCI-H460 (60772 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SF-268 (49410 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IGROV-1 (47897 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KM-20L2 (14967 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LOX IMVI (44321 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HOP-62 (47048 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LXFL 529 (14112 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
M19-MEL (15326 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Malme-3M (44254 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NCI-H23 (49055 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NCI-H522 (44358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SF-539 (44845 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504752509
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504752509
IUPAC Name 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione
INCHI 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
InChIKey KOMNUTZXSVSERR-UHFFFAOYSA-N
Smiles C=CCN1C(=O)N(C(=O)N(C1=O)CC=C)CC=C
Isomeric SMILES C=CCN1C(=O)N(C(=O)N(C1=O)CC=C)CC=C
WGK Germany 1
RTECS XZ1915000
PubChem CID 13931
UN Number 3077
Packing Group III
Molecular Weight 249.27
Beilstein 225482
Reaxy-Rn 225482

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

43 results found

Lot Number Certificate Type Date Item
E2521576 Certificate of Analysis May 08, 2025 T123406
E2526577 Certificate of Analysis May 08, 2025 T123406
E2521577 Certificate of Analysis May 08, 2025 T123406
E2521578 Certificate of Analysis May 08, 2025 T123406
B2510578 Certificate of Analysis Jan 07, 2025 T123406
B2510579 Certificate of Analysis Jan 07, 2025 T123406
B2510580 Certificate of Analysis Jan 07, 2025 T123406
A2508178 Certificate of Analysis Oct 15, 2024 T123406
J2424928 Certificate of Analysis Oct 15, 2024 T123406
J2424915 Certificate of Analysis Oct 15, 2024 T123406
J2424929 Certificate of Analysis Oct 15, 2024 T123406
F2427449 Certificate of Analysis Jun 15, 2024 T123406
F2427450 Certificate of Analysis Jun 15, 2024 T123406
F2427442 Certificate of Analysis Jun 15, 2024 T123406
K2413114 Certificate of Analysis Jun 15, 2024 T123406
K2422259 Certificate of Analysis Jun 15, 2024 T123406
C2407447 Certificate of Analysis Feb 28, 2024 T123406
C2407448 Certificate of Analysis Feb 28, 2024 T123406
A2423245 Certificate of Analysis Jan 31, 2024 T123406
A2423246 Certificate of Analysis Jan 31, 2024 T123406
A2423247 Certificate of Analysis Jan 31, 2024 T123406
A2423249 Certificate of Analysis Jan 31, 2024 T123406
L2318368 Certificate of Analysis Nov 23, 2023 T123406
L2318369 Certificate of Analysis Nov 23, 2023 T123406
H2309893 Certificate of Analysis Jul 24, 2023 T123406
H2309875 Certificate of Analysis Jul 24, 2023 T123406
H2309855 Certificate of Analysis Jul 24, 2023 T123406
D2304143 Certificate of Analysis Feb 17, 2023 T123406
D2304135 Certificate of Analysis Feb 17, 2023 T123406
A2305746 Certificate of Analysis Dec 17, 2022 T123406
A2305744 Certificate of Analysis Dec 17, 2022 T123406
A2305764 Certificate of Analysis Dec 17, 2022 T123406
A2305775 Certificate of Analysis Dec 17, 2022 T123406
A2305771 Certificate of Analysis Dec 17, 2022 T123406
A2305741 Certificate of Analysis Dec 17, 2022 T123406
H2217786 Certificate of Analysis Jul 23, 2022 T123406
H2217768 Certificate of Analysis Jul 23, 2022 T123406
H2217787 Certificate of Analysis Jul 23, 2022 T123406
H2217769 Certificate of Analysis Jul 23, 2022 T123406
E1804097 Certificate of Analysis Mar 25, 2022 T123406
B2216496 Certificate of Analysis Dec 06, 2021 T123406
B2216497 Certificate of Analysis Dec 06, 2021 T123406
B2216498 Certificate of Analysis Dec 06, 2021 T123406

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Chemical and Physical Properties

Solubility Insoluble in water, soluble in methanol, acetone, n-heptane, benzene.
Sensitivity Light sensitive
Refractive Index 1.513
Boil Point(°C) 140°C/6mmHg
Melt Point(°C) 24 °C
Molecular Weight 249.270 g/mol
XLogP3 1.300
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 6
Exact Mass 249.111 Da
Monoisotopic Mass 249.111 Da
Topological Polar Surface Area 60.900 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 331.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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