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BCR158

Benz[c]acridine

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C17H11N
Número de CAS:
225-51-4
Peso molecular:
229.28
Beilstein:
154999
Número MDL:
MFCD00215933
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329773794
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

c1ccc2nc3c(ccc4ccccc34)cc2c1

InChI

1S/C17H11N/c1-3-7-15-12(5-1)9-10-14-11-13-6-2-4-8-16(13)18-17(14)15/h1-11H

Clave InChI

OAPPEBNXKAKQGS-UHFFFAOYSA-N

Nota de análisis

For more information please see:
BCR158

Información legal

BCR is a registered trademark of European Commission

Pictogramas

CorrosionExclamation mark
GHS05,GHS07

Palabra de señalización

Danger

Frases de peligro

H302,H318

Clasificaciones de peligro

Acute Tox. 4 Oral - Eye Dam. 1

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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T Kurihara et al.
Anticancer research, 16(5A), 2757-2765 (1996-09-01)
In order to clarify the effects of methyl substitution on the carcinogenic activity, each resonance energy (RE) of benz[c]acridines, benzo[a]phenothiazines, chrysene, and their methyl derivatives was calculated by Aihara's TRE theory. Some correlations seem to exist between the values of
R L Chang et al.
Cancer research, 44(11), 5161-5164 (1984-11-01)
The tumorigenicity of benz[c]acridine (B[c]ACR) and a number of its derivatives, including the five metabolically possible transdihydrodiols, the diastereomeric bay-region diol-epoxides, two non-bay-region diol-epoxides, and the K-region 5,6-oxide, were assessed in newborn mice. A total dose of 0.50 or 1.05
K Satoh et al.
Anticancer research, 17(5A), 3553-3557 (1997-12-31)
Among 13 benz[c]acridines, six 7-methyl-substituted compounds (7-methylbenz[c]acridine, 7,9-dimethylbenz[c]acridine, 7,10-dimethylbenz[c]acridine, 7,11-dimethylbenz[c]acridine, 7,9,10-trimethylbenz[c]acridine, 7,9,11-trimethylbenz[c]acridine) were carcinogenic, while the other seven compounds (benz[c] acridine, 8-methylbenz[c]acridine, 9-methylbenz[c]acridine, 10-methylbenz[c]acridine, 11-methylbenz[c]acridine, 5,7-dimethylbenz[c]acridine, cis-5,6-dihydroxy-5,6-dihydrobenz[c]acridine) were inactive. Using both McLachlan-Hückel molecular orbital (McLachlan-HMO) and HMO methods, all the
N Motohashi et al.
Journal of chromatography, 643(1-2), 1-10 (1993-07-23)
Benz[c]acridine and many of its related compounds have been shown to exhibit carcinogenic activity. Unfortunately, these compounds are continually being found in many natural and environmental samples in widely divergent geographical locations. A review of chromatographic methods for mainly benz[c]acridine
Separation of methyl-substituted benz[c]acridines by reversed-phase high-performance thin-layer chromatography.
K Kamata et al.
Journal of chromatography, 396, 437-440 (1987-06-19)
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