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化驗
99%
形狀
solid
bp
280 °C (lit.)
mp
78-82 °C (lit.)
密度
0.899 g/mL at 25 °C (lit.)
SMILES 字串
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 密鑰
HXGDTGSAIMULJN-UHFFFAOYSA-N
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應用
Acenaphthylene has been used to investigate the photodimerization of acenaphthylene in micellar and hydrogel media.
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
251.6 °F - closed cup
閃點（°C）
122.0 °C - closed cup
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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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
An electron spin resonance study of the carbonization of the aromatic hydrocarbon acenaphthylene.
Singer LS and Lewis IC.
Carbon, 2(2), 115-120 (1964)
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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