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BCR269

Chrysene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C18H12
CAS Number:
218-01-9
Molecular Weight:
228.29
Beilstein:
1909297
EC Number:
205-923-4
MDL number:
MFCD00003698
UNSPSC Code:
41116107
PubChem Substance ID:
329773802
NACRES:
NA.24

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

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

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Analysis Note

For more information please see:
BCR269

Legal Information

BCR is a registered trademark of European Commission

Pictograms

Health hazardEnvironment
GHS08,GHS09

Signal Word

Danger

Hazard Statements

H341,H350,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Muta. 2

Storage Class Code

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

EU REACH Annex XVII (Restriction List)

CAS No.

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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
A I Alajtal et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 76(1), 1-5 (2010-03-24)
Raman spectroscopy, with visible laser (514 and 633 nm) and near infrared (785 and 1064 nm) excitation, has been used to obtain high quality spectra of phenanthrene, chrysene, and tetracene. Samples with dimensions from a minimum size of 10 microm
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
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
Theodoros Tzamkiozis et al.
Inhalation toxicology, 22 Suppl 2, 59-69 (2010-10-30)
This study presents different research techniques linked together to improve our understanding of the particulate matter (PM) impacts on health. PM samples from the exhaust of different vehicles were collected by a versatile aerosol concentration enrichment system (VACES). Waterborne PM
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