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融点 | 144-147 °C | 沸点 | 353°C [760mmHg] | 比重(密度) | 0.87 | 蒸気密度 | >1 (vs air) | 蒸気圧 | 0Pa at 25℃ | 闪点 | 129 °F | 貯蔵温度 | Inert atmosphere,Room Temperature | 外見 | Powder | 酸解離定数(Pka) | 12.06±0.53(Predicted) | 色 | white | 水溶解度 | reacts | Sensitive | Air & Light Sensitive | Hydrolytic Sensitivity | 4: no reaction with water under neutral conditions | BRN | 2523445 | 安定性: | Stable. Combustible. Incompatible with strong oxidizing agents. | LogP | 2 at 20℃ | CAS データベース | 947-42-2(CAS DataBase Reference) | NISTの化学物質情報 | Diphenyl silanediol(947-42-2) | EPAの化学物質情報 | Silanediol, diphenyl- (947-42-2) |
主な危険性 | F | Rフレーズ | 11-10 | Sフレーズ | 16-22-24/25-37-26 | RIDADR | UN 1325 4.1/PG 3 | WGK Germany | 1 | RTECS 番号 | VV3640000 | TSCA | Yes | 国連危険物分類 | 4.1 | 容器等級 | III | HSコード | 29319090 |
| ジフェニルシランジオール Usage And Synthesis |
外観 | 白色~ほとんど白色粉末~結晶 | 説明 | Diphenylsilanediol is a chemical compound that is used as a catalyst. It can be produced by the reaction of diphenylsilane with sulfuric acid. This chemical has been shown to have high thermal and chemical stability, making it an ideal material for catalytic materials. Diphenylsilanediol has also been shown to be an efficient solid catalyst for synthesizing hydrocarbons from hydrogen fluoride and hydrochloric acid. The efficiency of this catalyst may be due to its ability to reduce the activation energy required for the reaction. Diphenylsilanediol is an important material used to manufacture silicone resins and rubbers. In addition, it is helpful as an additive for organopolysiloxanes that are convertible to the cured solid.
| 化学的特性 | White powder | 使用 | Diphenylsilanediol is used in Medicine field, electronics industry and polymer material. | 製造方法 | Diphenylsilanediol was obtained by controlled hydrolysis of diphenyldichlorosilane in the presence of aniline as acid acceptor and ethyl ether . | 一般的な説明 | Diphenylsilanediol(DPSD) is an alkoxysilane that is used as a silane based precusor in the synthesis of organosiloxane based resins. | 燃焼性と爆発性 | Non flammable | 純化方法 | Recrystallise it from CHCl3/methyl ethyl ketone. [Beilstein 16 IV 1523.] |
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