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379506

Sigma-Aldrich

Tris(2,3-epoxypropyl) isocyanurate

Synonym(s):

1,3,5-Tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione, TGIC, Triglycidyl isocyanurate

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About This Item

Empirical Formula (Hill Notation):
C12H15N3O6
CAS Number:
2451-62-9
Molecular Weight:
297.26
EC Number:
219-514-3
MDL number:
MFCD00080670
UNSPSC Code:
12162002
PubChem Substance ID:
24863665
NACRES:
NA.23

form

powder

SMILES string

O=C1N(CC2CO2)C(=O)N(CC3CO3)C(=O)N1CC4CO4

InChI

1S/C12H15N3O6/c16-10-13(1-7-4-19-7)11(17)15(3-9-6-21-9)12(18)14(10)2-8-5-20-8/h7-9H,1-6H2

InChI key

OUPZKGBUJRBPGC-UHFFFAOYSA-N

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Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Muta. 1B - Skin Sens. 1 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

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Jing-Ping Wang et al.
Toxicology and applied pharmacology, 273(1), 110-120 (2013-08-21)
In this work, we demonstrated that the growth of human non-small-cell-lung-cancer cells H460 and A549 cells can be inhibited by low concentrations of an epoxide derivative, teroxirone, in both in vitro and in vivo models. The cytotoxicity was mediated by
Occupational contact dermatitis from triglycidyl isocyanurate in a powder paint sprayer.
J P McFadden et al.
Contact dermatitis, 28(4), 251-251 (1993-04-01)
Occupational contact dermatitis from triglycidyl isocyanurate in a powder paint factory.
C S Munro et al.
Contact dermatitis, 26(1), 59-59 (1992-01-01)
R Jolanki et al.
Contact dermatitis, 30(1), 12-15 (1994-01-01)
A 48-year-old female silk-screen printer had worked in the manufacture of circuit boards for 12 years before she got the first symptoms of dermatitis on her wrists and lower arms. On the 1st patch test session, epoxy resin and the
J A Neidhart et al.
Cancer treatment reports, 68(9), 1115-1119 (1984-09-01)
Teroxirone is a novel triepoxide, synthesized as an alkylator and showing a broad spectrum of preclinical activity. It has good cytotoxic activity against sublines of P388 and L1210 leukemias resistant to another alkylating agent, cyclophosphamide. Thirty-six patients received teroxirone as
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