BCR158
Benz[c]acridine
BCR®, certified reference material
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About This Item
Empirical Formula (Hill Notation):
C17H11N
CAS Number:
Molecular Weight:
229.28
Beilstein/REAXYS Number:
154999
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24
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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
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
InChI key
OAPPEBNXKAKQGS-UHFFFAOYSA-N
Related Categories
Analysis Note
For more information please see:
BCR158
BCR158
Legal Information
BCR is a registered trademark of European Commission
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_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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