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
产品名称
苊烯, analytical standard
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
wgk
WGK 3
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
K Schirmer et al.
Toxicology, 127(1-3), 129-141 (1998-08-12)
Sixteen polycyclic aromatic hydrocarbons (PAHs) were screened for their ability to be directly cytotoxic to a cell line from the rainbow trout gill, RTgill-W1. Exposure times of 2 h or less were sufficient for direct cytotoxicity to be detected, which
F J Rivas et al.
Journal of hazardous materials, 75(1), 89-98 (2000-06-01)
Removal of acenaphthylene from water has been carried out by means of different treatments combining UV radiation, ozone and hydrogen peroxide. Ozonation alone or in conjunction with hydrogen peroxide (10(-3) M) resulted in the highest elimination rates. Thus, conversions as
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