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| | 4-[[4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イル]アミノ]-2,6-ジ-tert-ブチルフェノール 製品概要 |
| 化学名: | 4-[[4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イル]アミノ]-2,6-ジ-tert-ブチルフェノール | | 英語化学名: | Antioxidant 565 | | 别名: | phenol,4-[[4,6-bis(octylthio)-1,3,5-triazin-2-yl]amino]-2,6-bis(1,1-dimethylet;2,6-di-tert-butyl-4-(4,6-bis(octylthio)-1,3,5-triazin-2-ylamino)phenol;4-[[4,6-bis(octylthio)-1,3,5-triazin-2-yl]amino]-2,6-bis(1,1-dimethylethyl)-Phenol;IRGANOX 565;6-(4-Hydroxy-3,5-di-tert-butylanilino)-2,4-bis(octylthio)-1,3,5-triazine;N-[2,4-Bis(octylthio)-1,3,5-triazine-6-yl]-3,5-di-tert-butyl-4-hydroxyaniline;UVA-AO;Antioxidant 565 | | CAS番号: | 991-84-4 | | 分子式: | C33H56N4OS2 | | 分子量: | 588.95 | | EINECS: | 213-590-1 | | カテゴリ情報: | Organics;Antioxidant series | | Mol File: | 991-84-4.mol | ![4-[[4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イル]アミノ]-2,6-ジ-tert-ブチルフェノール](CAS/GIF/991-84-4.gif) |
| | 4-[[4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イル]アミノ]-2,6-ジ-tert-ブチルフェノール 物理性質 |
| | 4-[[4,6-ビス(オクチルチオ)-1,3,5-トリアジン-2-イル]アミノ]-2,6-ジ-tert-ブチルフェノール Usage And Synthesis |
| 外観 | 白色～ほとんど白色粉末～結晶 | | 定義 | 本品は、次の化学式で表される有機化合物である。 | | 化粧品の成分用途 | 酸化防止剤 | | 化学的特性 | Antioxidant 565 is a highly effective antioxidant. It prevents gel formation, changes to molecular weight and maintains excellent polymer color in unsaturated elastomers. This grade is highly effective at low concentrations and matches the performance of other stabilizers at higher levels. It exhibits non-staining and low volatility. It allows easy dispersion due to low melting point in elastomeric substrates using melt compounding techniques. It can be incorporated into process streams by dissolving in suitable organic solvents or aromatic extender oils. | | 定義 | ChEBI: 4-((4,6-bis(octylthio)-1,3,5-triazin-2-yl)amino)-2,6-di-tert-butylphenol is a member of triazines. | | 燃焼性と爆発性 | Not classified | | 合成 | By taking 2,6-di-tert-butylphenol as the raw material, and then adding sodium nitrite solution dropwise to form an intermediate product of 2,6-di-tert-butyl-4-nitrosophenol solution, with the added Rayon Nickel is used as a catalyst and carbon monoxide is used instead of hydrogen as a reducing agent to overcome hydrogen as a reducing agent. The pressure in the hydrogenation process is high, which is prone to explosion problems. At the same time, iron crystals are added to remove excess carbon monoxide and avoid the effects of carbon monoxide toxicity. The impurities are removed by filtration, and other by-products will not be formed, which can greatly increase the yield of antioxidant 565, and the product purity is high. |
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