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等级
reagent grade
质量水平
蒸汽密度
4.55 (vs air)
蒸汽压
0.18 mmHg ( 20 °C)
方案
≥97%
表单
liquid
自燃温度
723 °F
expl. lim.
0.8 %, 100 °F
5 %, 150 °F
折射率
n20/D 1.541 (lit.)
沸点
207 °C (lit.)
mp
−35 °C (lit.)
密度
0.973 g/mL at 25 °C (lit.)
SMILES字符串
C1CCc2ccccc2C1
InChI
1S/C10H12/c1-2-6-10-8-4-3-7-9(10)5-1/h1-2,5-6H,3-4,7-8H2
InChI key
CXWXQJXEFPUFDZ-UHFFFAOYSA-N
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一般描述
Tetralin is a bicyclic molecule composed of an aromatic moiety and an alicyclic moiety that share two carbon atoms in common. It is used as a hydrogen-donor solvent in coal liquefaction. Tetralin is also used to synthesize agricultural chemicals. Additionally, it is used as a degreaser and solvent for fats, resins, and waxes and as a substitute for turpentine in paints, lacquers, and shoe polishes.
应用
1,2,3,4-Tetrahydronaphthalene is used as a:
- Hydrogen-donor solvent in the decarboxylation of oleic acid to produce diesel fuel hydrocarbons.
- Hydrogen source for the hydrogenation of lignin-derived phenolic compounds.
法律信息
警示用语：
Danger
危险分类
Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2
补充剂危害
储存分类代码
10 - Combustible liquids
WGK
WGK 2
闪点(°F)
159.8 °F - closed cup
闪点(°C)
71 °C - closed cup
法规信息
新产品
The Low-Temperature Thermodynamic Properties of Naphthalene, 1-Methylnaphthalene, 2-Methylnaphthalene, 1,2,3,4-Tetrahydronaphthalene, trans-Decahydronaphthalene and cis-Decahydronaphthalene.
McCullough JP, et al.
The Journal of Physical Chemistry, 61(8), 1105-1116 (1957)
Hydrogen production from tetralin over microwave-accelerated Pt-supported activated carbon.
Suttisawat Y, et al.
International Journal of Hydrogen Energy, 35(12), 6179-6183 (2010)
Fullerene production in sooting flames from 1,2,3,4-tetrahydronaphthalene.
Alford JM, et al.
Carbon, 46(12), 1623-1625 (2008)
Experimental and kinetic modeling study of tetralin pyrolysis at low pressure.
Li Y, et al.
Proceedings of the Combustion Institute, 34(1), 1739-1748 (2013)
Activated carbon supported molybdenum carbides as cheap and highly efficient catalyst in the selective hydrogenation of naphthalene to tetralin.
Pang M, et al.
Green Chemistry, 14(5), 1272-1276 (2012)
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