48565-U
Chrysene
analytical standard
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About This Item
Empirical Formula (Hill Notation):
C18H12
CAS Number:
Molecular Weight:
228.29
UNSPSC Code:
77101502
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-923-4
Beilstein/REAXYS Number:
1909297
MDL number:
grade
analytical standard
Quality Level
packaging
vial of 100 mg
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
448 °C (lit.)
mp
252-254 °C (lit.)
application(s)
cleaning products
cosmetics
environmental
food and beverages
personal care
format
neat
storage temp.
room temp
SMILES string
c1ccc2c(c1)ccc3c4ccccc4ccc23
InChI
1S/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H
InChI key
WDECIBYCCFPHNR-UHFFFAOYSA-N
Application
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
Danger
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Muta. 2 - PBT - vPvB
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Daoud Ali et al.
Toxicology letters, 204(2-3), 199-207 (2011-05-17)
Chrysene is one of the basic polycyclic aromatic hydrocarbon (PAH) which is toxic environmental pollutant and consistently exposed to sunlight. However, little information is available on its photogenotoxicity. The objective of the present study was to analyze the effects of
Valentina Calabrese et al.
Chemical communications (Cambridge, England), 46(44), 8374-8376 (2010-10-07)
7-N,N-Dibutylamino-2-azaphenanthrene (L(3)), 8-N,N-dibutylamino-2-azachrysene (L(4)) and related Ir(i) complexes or alkylated salts show high second-order NLO responses, as determined by the EFISH technique and DFT calculations. L(4) is appealing as building block for NLO active materials due to its unexpected large
Peter A Lieberzeit et al.
Analytical and bioanalytical chemistry, 392(7-8), 1405-1410 (2008-11-06)
Molecular imprinting with binary mixtures of different polycyclic aromatic hydrocarbons (PAH) is a tool for design of chemically highly sensitive layers for detection of these analytes. Sensor responses increase by one order of magnitude compared with layers imprinted with one