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Merck
CN

379506

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:
Molecular Weight:
297.26
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
219-514-3
MDL number:
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InChI key

OUPZKGBUJRBPGC-UHFFFAOYSA-N

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

SMILES string

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

form

powder

Quality Level

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signalword

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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U Erikstam et al.
Contact dermatitis, 44(1), 13-17 (2001-01-13)
Triglycidyl isocyanurate (TGIC) is mainly used in polyester-based powder paints, but also in laminates, insulating varnishes, coatings and adhesives. Several cases of contact allergy to TGIC have been reported during the last 10 years. Contact allergy to TGIC has developed
J Rubin et al.
Cancer treatment reports, 71(5), 489-492 (1987-05-01)
Two schedules of teroxirone, a triazine triepoxide, were evaluated in a phase I study. Twenty-six patients were treated on 1 day every 5 weeks at doses of 36-2250 mg/m2. At doses greater than or equal to 1500 mg/m2, severe thrombophlebitis
Airborne contact dermatitis due to triglycidylisocyanurate.
A Dooms-Goossens et al.
Contact dermatitis, 21(3), 202-203 (1989-09-01)
Occupational contact allergy to triglycidyl isocyanurate (TGIC, Tepic).
K Nishioka et al.
Contact dermatitis, 19(5), 379-380 (1988-11-01)
M M Ames et al.
Cancer research, 44(9), 4151-4156 (1984-09-01)
Teroxirone is an experimental triepoxide antitumor agent currently undergoing evaluation in clinical trials. We have developed an assay based on derivatization with diethyldithiocarbamate followed by normal-phase high-performance liquid chromatographic analysis. When 14C-labeled teroxirone is administered to rabbits by rapid i.v.

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