48566
苊烯
analytical standard
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关于此项目
经验公式（希尔记法）:
C12H8
化学文摘社编号:
分子量:
152.19
EC Number:
205-917-1
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
774092
MDL number:
NACRES:
NA.24
InChI key
HXGDTGSAIMULJN-UHFFFAOYSA-N
InChI
1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H
SMILES string
c1cc2C=Cc3cccc(c1)c23
grade
analytical standard
CofA
current certificate can be downloaded
packaging
ampule of 100 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
280 °C (lit.)
mp
78-82 °C (lit.)
density
0.899 g/mL at 25 °C (lit.)
application(s)
environmental
format
neat
storage temp.
2-30°C
Quality Level
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Application
Acenaphthylene may be used as an analytical reference standard for the determination of the analyte in water using gas chromatography-flame ionization detection (GC-FID).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
flash_point_f
251.6 °F - closed cup
flash_point_c
122.0 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Determination of organic compounds in water using dispersive liquid-liquid microextraction.
Rezaee M, et al.
Journal of Chromatography A, 1116(1-2), 1-9 (2006)
E Leonhardt et al.
Analytical chemistry, 70(6), 1228-1230 (1998-04-08)
Polycyclic aromatic hydrocarbons were extracted from a soil sample using ultrasound and dichloromethane-, cyclohexane-, and toluene-water mixtures. It was found that when dichloromethane is used as an extractant, acenaphthylene reacts with the solvent. Several chlorinated and oxygenated derivatives were identified.
Yan Hao et al.
Organic & biomolecular chemistry, 10(4), 724-728 (2011-12-15)
A simple and novel protocol for the efficient synthesis of a series of 8-carboxylnaphthyl functionalized pyrazolo[3,4-b]pyridine derivatives was developed through a one-pot, three-component reaction involving acenaphthylene-1,2-dione and 1H-pyrazol-5-amine in acetic acid medium. The reaction represents the first facile conversion of
Dong Wang et al.
The Journal of organic chemistry, 71(22), 8365-8371 (2006-10-27)
Polycyclic aromatic hydrocarbon growth from acenaphthylene and cyclopentadienyl was investigated by using the B3LYP/6-31G(d,p) and BH&HLYP/6-31G(d,p) levels of theory as well as transition state theory. The reaction pathways of cyclopentadienyl bearing hydrocarbons are different from those without these moieties and
Ming Chen et al.
Chemical communications (Cambridge, England), (9)(9), 1112-1114 (2008-02-23)
A higher efficiency of excitation energy transfer occurs to a luminescent diphenylanthracenyl acceptor incorporated at the centre, rather than the end, of an acenaphthylene polymer chain.
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