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BCR168

Picene

BCR®, certified reference material

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About This Item

CAS Number:
213-46-7
UNSPSC Code:
41116107
NACRES:
NA.21
PubChem Substance ID:
329773797
MDL number:
MFCD00215857
Beilstein/REAXYS Number:
1912414

Key Documents

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InChI

1S/C22H14/c1-3-7-17-15(5-1)9-11-21-19(17)13-14-20-18-8-4-2-6-16(18)10-12-22(20)21/h1-14H

SMILES string

c1ccc2c(c1)ccc3c2ccc4c5ccccc5ccc34

InChI key

GBROPGWFBFCKAG-UHFFFAOYSA-N

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

environmental
pharmaceutical (small molecule)

format

neat

storage temp.

room temp

Analysis Note

For more information please see:
BCR168

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H351

Hazard Classifications

Carc. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

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Andrew P Rutter et al.
Environmental science & technology, 43(20), 7770-7777 (2009-11-20)
Carbonaceous atmospheric particulate matter (PM25) collected in the midwestern United States revealed that soot emissions from incomplete coal combustion were important sources of several organic molecular markers used in source apportionment studies. Despite not constituting a major source of organic
K L Platt et al.
Carcinogenesis, 11(10), 1721-1726 (1990-10-01)
The carcinogenic activity of the two polycyclic aromatic hydrocarbons (PAHs), picene (benzo[a]chrysene) and dibenz[a,h]anthracene (DBA), was determined in NMRI mice by five different experimental protocols in order to find out if picene is a carcinogen as predicted by recent quantum
K L Platt et al.
Chemico-biological interactions, 66(3-4), 157-175 (1988-01-01)
Picene, a polycyclic aromatic hydrocarbon (PAH) of environmental relevance has recently been predicted to be carcinogenic, based on quantum mechanical calculation, although in several animal studies no carcinogenicity could be detected. In order to find out if the metabolism of
Gunzi Saito et al.
Chemical record (New York, N.Y.), 11(3), 124-145 (2011-06-01)
The present status of organic superconductors of charge-transfer (CT) type based on donor molecules is reviewed. Along with the superconducting phases of such materials and also of oxide superconductors, reside spin-ordered phases such as spin-density wave (SDW) and antiferromagnetic (AF)
F J Zhang et al.
The Journal of organic chemistry, 65(13), 3952-3960 (2000-06-24)
A new synthetic approach to polycyclic aromatic compounds is described that entails in the key steps double Suzuki coupling of PAH bisboronic acid derivatives with o-bromoaryl aldehydes to furnish aryl dialdehydes that are converted to larger polycyclic aromatic ring systems
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