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| 2,2'-ジベンゾチアゾリルジスルフィド 製品概要 |
| 2,2'-ジベンゾチアゾリルジスルフィド 物理性質 |
融点 | 177-180 °C (lit.) | 沸点 | 532.5±33.0 °C(Predicted) | 比重(密度) | 1.5 | 蒸気圧 | 0Pa at 25℃ | 屈折率 | 1.5700 (estimate) | 闪点 | 271°C | 貯蔵温度 | Keep in dark place,Sealed in dry,Room Temperature | 溶解性 | 0.01g/l | 酸解離定数(Pka) | -0.58±0.10(Predicted) | 外見 | powder to crystal | 色 | Cream to pale-yellow powder | 臭い (Odor) | gray-wh. to cream powd. or pellets, sl. odor | 水溶解度 | <0.01 g/100 mL at 21 ºC | Merck | 14,3370 | InChIKey | AFZSMODLJJCVPP-UHFFFAOYSA-N | LogP | 4.5 at 20℃ | CAS データベース | 120-78-5(CAS DataBase Reference) | NISTの化学物質情報 | Benzothiazyl disulfide(120-78-5) | EPAの化学物質情報 | 2,2'-Dithiobisbenzothiazole (120-78-5) |
| 2,2'-ジベンゾチアゾリルジスルフィド Usage And Synthesis |
外観 | 白色~黄赤色~緑色粉末~結晶 | 用途 | 中間物、ゴム用添加剤、樹脂用添加剤、有機ゴム薬品(加硫促進剤) | 説明 | Dibenzothiazyl disulfide is a rubber chemical used as a
vulcanization accelerant. The most frequent occupational
categories are metal industry, homemakers,
health services and laboratories, and building industries. | 化学的特性 | yellow amorphous powder | 使用 | Dibenzothiazyl disulfide is an accelerator for natural rubber, nitrile-butadiene, butyl and styrene-butadiene rubber; a retarder for chloroprene rubber. | 使用 | 2,2’Dibenzothiazoyl Disulfide has the potential to combat HPV, acting as a zinc-ejecting inhibitor. It also can act as radical polymerization photo-initiators or co-initiators. | 定義 | ChEBI: An organic disulfide resulting from the formal oxidative coupling of the thiol groups of two molecules of 1,3-benzothiazole-2-thiol. It is used as an accelerator in the rubber industry. | 一般的な説明 | Cream to light yellow powder. | 空気と水の反応 | Insoluble in water. | 反応プロフィール | 2,2'-Dithiobis(benzothiazole) is incompatible with strong oxidizers. . | 火災危険 | 2,2'-Dithiobis(benzothiazole) is combustible. | 接触アレルゲン | This rubber chemical of the mercaptobenzothiazole group
is used as a vulcanization accelerant. The most frequent occupational categories are metal industry, homemakers,
health services and laboratories, and the building industry. | 安全性プロファイル | Poison by intravenous andintraperitoneal routes. Slightly toxic by ingestion.Experimental teratogenic and reproductive effects.Questionable carcinogen with experimental tumorigenicdata. Mutation data reported. When heated todecomposition it emits ver |
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