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Merck
CN

BCR269

BCR®, certified reference material

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经验公式(希尔记法):
C18H12
化学文摘社编号:
分子量:
228.29
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-923-4
Beilstein/REAXYS Number:
1909297
MDL number:
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InChI key

WDECIBYCCFPHNR-UHFFFAOYSA-N

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

SMILES string

c1ccc2c(c1)ccc3c4ccccc4ccc23

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

448 °C (lit.)

mp

252-254 °C (lit.)

format

neat

storage temp.

2-8°C

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General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Analysis Note

For more information please see:
BCR269

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardEnvironment

signalword

Danger

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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
L Viñas et al.
Chemosphere, 75(4), 534-541 (2009-01-20)
Aliphatic and aromatic hydrocarbons were determined in three species of commercial shellfish, namely razor shells (Ensis arcuatus and Ensis siliqua), goose barnacle (Pollicipes cornucopia) and sea urchin (Paracentrotus lividus), living in different habitats and exhibiting different feeding behaviors. The samples
Bimal K Banik et al.
European journal of medicinal chemistry, 45(10), 4687-4691 (2010-08-13)
We describe herein the synthesis of novel 6,12-distributed chrysene as potent anticancer agents. In vitro and in vivo studies are also reported here.

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