Tetralin (1,2,3,4-tetrahydronaphthalene) is a hydrocarbon having the chemical formula C 10 H 12. It is a partially hydrogenated derivative of naphthalene . It is a colorless liquid that is used as a hydrogen-donor solvent .

大量用于制造杀虫剂西维因的中间体甲萘酚；还用以制造润滑剂，以及用来降低高黏度油的黏度，并广泛用作有机物（树脂、蜡、油脂、油漆、塑料等）的溶剂。 还可用于煤气工业中溶 …

四氢化萘 （英語： Tetralin），又稱 萘滿， 化學式 为C 10 H 12，由一个 苯 环和一个 环己烷 并合而成，可看作 萘 中一个环被完全 加氢 得到的产物。 工业上，氢气在 铂 催化下，对 萘 的部分氢化来生产四氢化萘。 人们就如何将萘氢化为四氢化萘做了大量的工作，最终的产物中随着反应的压强和温度的变化，会得到不同比例的萘、四氢化萘、 十氢化萘 的混合物。 如果使用CoO + MoO 3 + Al 2 O 3 或WS 2 + NiS + Al 2 O 3 作为催化剂，则温度应控制在300-370℃。 四氢化萘常被 …

It is an ortho-fused bicyclic hydrocarbon and a member of tetralins. It derives from a hydride of a naphthalene. See also: ... View More ... 1,2,3,4-tetrahydronaphthalene. Computed by Lexichem TK 2.7.0 (PubChem release 2021.10.14) InChI=1S/C10H12/c1-2-6-10-8-4-3-7-9 (10)5-1/h1-2,5-6H,3-4,7-8H2. Computed by InChI 1.0.6 (PubChem release 2021.10.14)

2025年2月5日 · 其制备方法是用萘为原料，在钼酸镍催化剂存在下，压力2.9 MPa，温度300℃，于绝热反应装置中进行加氢反应，得到的粗品进行精馏得产品。 TOKYO CHEMICAL INDUSTRY CO., LTD. ChemicalBook 为您提供1,2,3,4-四氢萘 (119-64-2)的化学性质，熔点，沸点，密度，分子式，分子量，物理性质，毒性，结构式，海关编码等信息，同时您还可以浏览1,2,3,4-四氢萘 (119-64-2)产品的价格，供应商，贸易商，生产企业和生产厂家，最后1,2,3,4-四氢萘 …

2019年10月23日 · CID 139244968 | C30H36 | CID 139244968 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

1,2,3,4-Tetrahydronaphthalene (Tetralin), a bicyclic hydrocarbon, is a constituent of petroleum and coal tar. It is used in coal liquefaction and as an alternative to turpentine in paints and waxes. Degradation of tetralin by Corynebacterium sp. strain C125, and by pyrolysis have been reported.

1，2，3，4-四氢化萘是制备甲萘酚的重要中间体，由此可以合成甲萘胺、敌草胺等农药。 检验锰。 脱脂剂。 中间体。 萘、油类和树脂的溶剂。 −35 °C (lit.) 储存于阴凉、通风的库房。 远离 …

Tetralin (1,2,3,4-tetrahydronaphthalene) is a bicyclic molecule composed of an aromatic and an alicyclic ring. It is naturally found in different crude oil reservoirs and also produced for industrial purposes from naphthalene by catalytic hydrogenation or from anthracene by cracking.

2010年2月6日 · Notes. Go To: Top Data from NIST Standard Reference Database 69: NIST Chemistry WebBook The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment.