416703
Acenaphthylene
99%
Synonym(s):
Cyclopenta[de]naphthalene
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100 MG
€134.00
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100 MG
€134.00
About This Item
Empirical Formula (Hill Notation):
C12H8
CAS Number:
Molecular Weight:
152.19
Beilstein:
774092
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
bp
280 °C (lit.)
mp
78-82 °C (lit.)
density
0.899 g/mL at 25 °C (lit.)
SMILES string
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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Application
Acenaphthylene has been used to investigate the photodimerization of acenaphthylene in micellar and hydrogel media.[1]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
251.6 °F - closed cup
Flash Point(C)
122.0 °C - closed cup
Personal Protective Equipment
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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