A104
Acenaphthene
97%
Synonym(s):
1,8-Ethylenenaphthalene
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About This Item
Empirical Formula (Hill Notation):
C12H10
CAS Number:
Molecular Weight:
154.21
Beilstein:
386081
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
vapor density
5.32 (vs air)
vapor pressure
10 mmHg ( 131 °C)
Assay
97%
form
solid
bp
279 °C (lit.)
mp
90-94 °C (lit.)
SMILES string
C1Cc2cccc3cccc1c23
InChI
1S/C12H10/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-6H,7-8H2
InChI key
CWRYPZZKDGJXCA-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
257.0 °F - closed cup
Flash Point(C)
125.0 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Yanzheng Gao et al.
Journal of environmental quality, 40(2), 653-656 (2011-04-28)
The subcellular process and distribution of polycyclic aromatic hydrocarbons (PAHs) in arbuscular mycorrhizal plants remains to be elucidated. This work used a greenhouse experiment to show that, accompanied by the apoplastic and symplastic water movement through the root, acenaphthene (ACE)
Ningjing Hu et al.
Environmental science and pollution research international, 18(2), 163-172 (2010-06-26)
The levels and possible sources of 16 polycyclic aromatic hydrocarbons (PAHs) were investigated in the surface sediments of Liaodong Bay, Bohai Sea, China. The sum of 16 PAHs (∑PAH(16)) concentrations varied from 144.5 to 291.7 ng/g, with a mean value
Di Wu et al.
Biomedical and environmental sciences : BES, 20(4), 291-294 (2007-10-24)
To investigate the oxidation of acenaphthene (Ace), a polycyclic aromatic hydrocarbon (PAH) with a saturated C-C bond by ozone and to characterize the intermediate products of ozonation. Ozone was generated from filtered dry oxygen by an ozone generator and continually
Fergus R Knight et al.
Dalton transactions (Cambridge, England : 2003), 41(11), 3154-3165 (2012-02-01)
Sterically crowded peri-substituted selenium and tellurium acenaphthene donors D1-D7 [Acenap(EPh)(Br) E = Se, Te; Acenap(SePh)(EPh) E = Se, S; Acenap(TePh)(EPh) E = S, Se, Te] react with dibromine and diiodine acceptors to afford a group of structurally diverse addition products
Zhipei Qin et al.
Journal of chromatography. A, 1196-1197, 89-95 (2008-04-22)
The characterization of a poly(dimethylsiloxane) (PDMS) thin film for active extraction of some polycyclic aromatic hydrocarbons was investigated in both a 1-L aqueous solution and a flow-through system. The thin film was attached to an electric bench-drill at a constant
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