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BCR077R

1-Methylchrysene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C19H14
CAS Number:
Molecular Weight:
242.31
Beilstein:
2557418
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

SMILES string

Cc1cccc2c1ccc3c4ccccc4ccc23

InChI

1S/C19H14/c1-13-5-4-8-17-15(13)11-12-18-16-7-3-2-6-14(16)9-10-19(17)18/h2-12H,1H3

InChI key

LQKGSLMFGWWLIU-UHFFFAOYSA-N

General description

1-Methylchrysene is a methyl derivative of chrysene, belonging to the class of polycyclic aromatic hydrocarbons (PAHs). It is found to be carcinogenic, mutagenic, toxic, and persistent in the environment.

Application

1-Methylchrysene may be used as certified reference material for the quantification of the analyte in soil samples and fish using gas chromatography followed by mass spectrometric analysis.

Analysis Note

For more information please see:
BCR077R

Legal Information

BCR is a registered trademark of European Commission

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Simplified and rapid determination of polychlorinated biphenyls, polybrominated diphenyl ethers, and polycyclic aromatic hydrocarbons in fish and shrimps integrated into a single method
Kalachova K, et al.
Analytica Chimica Acta, 707(1-2), 84-91 (2011)
Occurrence and leachability of polycyclic aromatic compounds in contaminated soils: Chemical and bioanalytical characterization
Larsson M, et al.
The Science of the Total Environment, 622, 1476-1484 (2018)
Sangwoo Lee et al.
Environmental science. Processes & impacts, 19(9), 1117-1125 (2017-08-08)
Polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs are known to be major toxic contaminants in spills of petroleum hydrocarbons (oil). Spilled oil undergoes weathering and over time, PAHs go through a series of compositional changes. PAHs can disrupt endocrine functions

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