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BCR140

Benzo[c]chrysene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C22H14
Número de CAS:
194-69-4
Peso molecular:
278.35
Beilstein:
1876196
Número MDL:
MFCD00667762
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329774229
NACRES:
NA.24

grado

certified reference material

Agency

BCR®

fabricante / nombre comercial

JRC

técnicas

HPLC: suitable
gas chromatography (GC): suitable

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

c1ccc2c(c1)ccc3c2ccc4ccc5ccccc5c34

InChI

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

Clave InChI

YZWGEMSQAMDWEM-UHFFFAOYSA-N

Nota de análisis

For more information please see:
BCR140

Información legal

BCR is a registered trademark of European Commission

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

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Certificados de análisis (COA)

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Shantu Amin et al.
Chemical research in toxicology, 16(2), 227-231 (2003-02-18)
Benzo[c]chrysene (BcC), an environmental pollutant, is a unique polycyclic aromatic hydrocarbon that possesses both a bay region and a fjord region in the same molecule. We previously demonstrated that both bay region and fjord region terminal rings are involved in
A Pal et al.
FEBS letters, 486(2), 163-166 (2000-12-13)
Carcinogenic activity of many polycyclic aromatic hydrocarbons (PAHs) is mainly attributed to their respective diol epoxides, which can be classified as either bay or fjord region depending upon the location of the epoxide function. The Pi class human glutathione (GSH)
A Luch et al.
Carcinogenesis, 19(4), 639-648 (1998-05-26)
Metabolic activation of the racemic benzo[c]chrysene-trans-9,10-, benzo[g]chrysene-trans-11,12- and dibenzo[a,l]pyrene-trans-11,12-dihydrodiols to fjord region syn- and anti-dihydrodiol epoxides by microsomes of Aroclor 1254-treated Sprague-Dawley rats has been examined. Since the fjord region dihydrodiol epoxides were hydrolytically unstable under the experimental conditions, their
A S Giles et al.
Chemical research in toxicology, 10(11), 1275-1284 (1997-12-24)
The metabolic activation in mouse skin of benzo[c]chrysene (B[c]C), a weakly carcinogenic polycyclic aromatic hydrocarbon (PAH) present in coal tar and crude oil, was investigated. Male Parkes mice were treated topically with 0.5 mumol of B[c]C, and DNA was isolated
Federica Nalin et al.
Analytical and bioanalytical chemistry, 410(3), 1123-1137 (2017-11-10)
Retention indices (I) for 45 polycyclic aromatic hydrocarbons (PAHs) and 63 methyl-substituted PAHs were determined by gas chromatography - mass spectrometry (GC-MS) using two different stationary phases: a Rxi-PAH phase (a "higher phenyl-content stationary phase") and a 50% (mole fraction)

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