48566
Acenaphthylene
analytical standard
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About This Item
Empirical Formula (Hill Notation):
C12H8
CAS Number:
Molecular Weight:
152.19
EC Number:
205-917-1
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
774092
MDL number:
NACRES:
NA.24
grade
analytical standard
Quality Level
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
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
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.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
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
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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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 48566 | 04061838086518 |