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CAS番号. | 93-45-8 |
化学名: | N-(p-ヒドロキシフェニル)-2-ナフタレンアミン |
别名: | p-オキシノゾン;4-(2-ナフチルアミノ)フェノール;N-(p-ヒドロキシフェニル)-2-ナフタレンアミン |
英語化学名: | N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97 |
英語别名: | p-Oxinozon;p-Oxyneozone;p-Hydroxyneozon;Paraoxyneozone.;p-Hydroxyneozone;C.I.Sulphur Black 6;Sulphur Vat Black CLG;4-(2-Naftylamino)fenol;4-(2-Naphtylamino)phenol;4-(2-Naphthylamino)phenol |
CBNumber: | CB9498976 |
分子式: | C16H13NO |
分子量: | 235.28052 |
MOL File: | 93-45-8.mol |
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N-(p-ヒドロキシフェニル)-2-ナフタレンアミン 物理性質 |
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安定性:: |
Stable. Incompatible with strong oxidizing agents. |
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N-(p-ヒドロキシフェニル)-2-ナフタレンアミン 化学特性,用途語,生産方法 |
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空気と水の反応
N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97 may be sensitive to prolonged exposure to air. Insoluble in water. |
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反応プロフィール
Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid. |
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健康ハザード
ACUTE/CHRONIC HAZARDS: When heated to decomposition N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97 emits toxic fumes. |
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火災危険
Flash point data for N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97 are not available, however, N-(4-HYDROXYPHENYL)-2-NAPHTHYLAMINE, 97 is probably combustible. |
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N-(p-ヒドロキシフェニル)-2-ナフタレンアミン 上流と下流の製品情報 |
原材料
4-アミノフェノール
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準備製品
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N-(p-ヒドロキシフェニル)-2-ナフタレンアミン 生産企業 Global( 21)Suppliers |
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