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蒸汽密度
4.55 (vs air)
质量水平
蒸汽压
0.18 mmHg ( 20 °C)
产品线
ReagentPlus®
方案
99%
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
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. A study reports the transformation of naphthalene to tetralin in the presence of activated carbon supported molybdenum carbides. Dehydrogenation of tetralin by microwave heating in the presence of platinum-supported activated carbon has been investigated.
应用
1,2,3,4-Tetrahydronaphthalene may be used as a raw material in the synthesis of fullerenes.
其他说明
存储中颜色可能变深
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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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
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)
Fullerene production in sooting flames from 1,2,3,4-tetrahydronaphthalene.
Alford JM, et al.
Carbon, 46(12), 1623-1625 (2008)
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)
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)
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)
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