| Identification | More | [Name]
Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate | [CAS]
27676-62-6 | [Synonyms]
1,3,5-TRIS(3,5-DITERT-BUTYL-4-HYDROXYBENZYL)-S-TRIAZINE-2,4,6-(1H,3H,5H)TRIONE
IRGANOX 3114
TRIS-(3,5-DI-T-BUTYL-4-HYDROXYBENZYL) ISOCYANURATE
TRIS(3,5-DI-TERT-BUTYL-4-HYDROXYBENZYL) ISOCYANURATE
TTIC
VANOX GT
1,3,5-triazine-2,4,6(1h,3h,5h)-trione,1,3,5-tris[[3,5-bis(1,1-dimethylethyl)-4
3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-tris[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]1
Antioxidant3114
-hydroxyphenyl]methyl]-
tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanur
RALOX 3114
Tris(3,5-Di-Tert-4-Hydroxybenzyl)Isocyanurate
1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione
1,3,5-Tris(3,5-di-tert-butyl-4-hydroxy benzyl)-s-Triazine-2,4,6-(1H,3H,5H)Trion
TRIS(3 5-DI-TERT-BUTYL-4-HYDROXYBENZYL)&
TRIS(3,5-DI-TERT-BUTYL-4-HYDROXYBENZYL) ISOCYANURATE 99%
Thanox3114
1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-tris3,5-bis(1,1-dimethylethyl)-4-hydroxyphenylmethyl-
1,3,5-TRIS(3,5-DI-TERT-BUTYL-4-HYDROXYBENZYL)-1,3,5-TRIAZI. | [EINECS(EC#)]
248-597-9 | [Molecular Formula]
C48H69N3O6 | [MDL Number]
MFCD00134700 | [Molecular Weight]
784.08 | [MOL File]
27676-62-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
218-220 °C(lit.)
| [Boiling point ]
757.9±60.0 °C(Predicted) | [density ]
1.03g/cm3 | [vapor pressure ]
0Pa@25°C | [Fp ]
289°C | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly, Heated), Methanol (Slightly, Heated) | [form ]
neat | [pka]
11.45±0.40(Predicted) | [color ]
White to Off-White | [Water Solubility ]
40μg/L at 20℃ | [InChIKey]
VNQNXQYZMPJLQX-UHFFFAOYSA-N | [SMILES]
N1(CC2=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C2)C(=O)N(CC2=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C2)C(=O)N(CC2=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C2)C1=O | [LogP]
15.18 | [CAS DataBase Reference]
27676-62-6(CAS DataBase Reference) | [EPA Substance Registry System]
27676-62-6(EPA Substance) |
| Questions And Answer | Back Directory | [Features]
Antioxidant 3114 is a hindered phenol antioxidant with light and heat stability, low volatility and anti-aging properties. It can produce synergistic effects when used in combination with UV absorbers and phosphites. |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Tris(3,5-di-tert-butyl-4-hydroxybenzyl) Isocyanurate(Antioxidant3114) is used an as antioxidant-stabilizer in polyolefin films intended for packaging nonfatty food as well as an antioxidant in propylene copolymers.
 | [General Description]
Antioxidant 3114, chemically known as Tris(3,5-di-tert-butyl-4-hydroxybenzyl) isocyanurate, serves as an effective antioxidant and UV stabilizer. It is extensively utilized in various materials including polyethylene, polypropylene, polystyrene, ABS resin, polyester, nylon, polyurethane, rubber, adhesives, petroleum resins, coatings, and oils. Additionally, it functions as a free radical scavenger to enhance the stability of polyolefins. | [Flammability and Explosibility]
Nonflammable(100%) | [Synthesis]
To a 1L autoclave equipped with a mechanical stirrer, a thermometer socket, a manometer and a nitrogen displacement port, 178 g of 2,6-di-tert-butylphenol, 24.48 g of paraformaldehyde, 41.28 g of isocyanuric acid, and 4.4 g of urotropine were added sequentially. The system was vacuumed and nitrogen replacement was repeated more than three times, and after the last nitrogen replacement, 1000 mL of 70% v/v methanol aqueous solution was pumped into the reactor under -0.01 MPa negative pressure. Subsequently, the system was charged with nitrogen to a pressure of 0.6 MPa. Under the nitrogen atmosphere, the temperature was gradually increased to 120°C and maintained for 2 hours, and then continued to increase to 140°C and maintained for 4 hours to complete the reaction. At the end of the reaction, the reactor was cooled to 58°C by circulating water to obtain the crude product. After the crude product was filtered, the solid was dissolved in 70% by volume methanol aqueous solution, cooled and recrystallized. The recrystallized product was washed at least twice with anhydrous methanol at 55 °C and dried to give the white crystalline target product, hindered phenolic antioxidant 3114, in 92.3% yield. | [References]
[1] Patent: CN108707122, 2018, A. Location in patent: Paragraph 0020; 0021; 0028; 0029 |
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