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质量水平
方案
99%
表单
solid
沸点
280 °C (lit.)
mp
78-82 °C (lit.)
密度
0.899 g/mL at 25 °C (lit.)
SMILES字符串
c1cc2C=Cc3cccc(c1)c23
InChI
1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H
InChI key
HXGDTGSAIMULJN-UHFFFAOYSA-N
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应用
Acenaphthylene has been used to investigate the photodimerization of acenaphthylene in micellar and hydrogel media.
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
251.6 °F - closed cup
闪点(°C)
122.0 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
An electron spin resonance study of the carbonization of the aromatic hydrocarbon acenaphthylene.
Singer LS and Lewis IC.
Carbon, 2(2), 115-120 (1964)
Durairajan Madhavan et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(2), 95-97 (2003-04-01)
The photochemical dimerisation of acenaphthylene in the presence of various cation-exchanged bentonite clays has been studied. While the cis-dimer is the predominant product when smaller cations are present in the clay interlayer, the presence of heavier atoms in the clay
Kinetics and products of the gas-phase reactions of acenaphthene with hydroxyl radicals, nitrate radicals and ozone.
Zhou S and Wenger JC.
Atmospheric Environment, 72, 97-104 (2013)
M J Schocken et al.
Applied and environmental microbiology, 48(1), 10-16 (1984-07-01)
A Beijerinckia sp. and a mutant strain, Beijerinckia sp. strain B8/36, were shown to cooxidize the polycyclic aromatic hydrocarbons acenaphthene and acenaphthylene. Both organisms oxidized acenaphthene to the same spectrum of metabolites, which included 1-acenaphthenol, 1-acenaphthenone, 1,2-acenaphthenediol, acenaphthenequinone, and a
Philipp Eyring et al.
Journal of separation science, 44(2), 600-608 (2020-11-14)
Food can contain unwanted compounds and need to be analyzed for compounds like carcinogenic polycyclic aromatic hydrocarbons to ensure consumer safety. The analytes need to be extracted from the sample matrix and cleaned-up to enable detection. However, established methods for
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