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BCR158

Benz[c]acridine

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C17H11N
CAS Number:
225-51-4
Molecular Weight:
229.28
Beilstein:
154999
MDL number:
MFCD00215933
UNSPSC Code:
41116107
PubChem Substance ID:
329773794
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

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

Analysis Note

For more information please see:
BCR158

Legal Information

BCR is a registered trademark of European Commission

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H318

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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J Molnár et al.
In vivo (Athens, Greece), 9(5), 463-468 (1995-09-01)
The endotoxin neutralizing effects of several phenothiazines, benzophenothiazines and Pentaglobin (control) were investigated by spectrophotometry, tumor necrosis factor (TNF) induction and the conventional Limulus test. In animal experiments, some beneficial effects of complex forming compounds were found, however, the compounds
K Kamata et al.
Neoplasma, 33(3), 313-322 (1986-01-01)
The 1H NMR spectra of benz[c]acridine and its methyl derivatives (BAc) in CDCl3 have been measured. The total assignment of 1H NMR spectra and spin coupling constants of BAc were discussed. The good relationship between the delta delta (delta 2--delta
J Molnar et al.
Anticancer research, 13(2), 439-442 (1993-03-01)
Some non-differentiation-induction benzo[a]phenothiazines and mutagenic benz[c]acridines more potently inhibited the mitogen-induced blast transformation of human-peripheral blood lymphocytes than differentiation-induction and non-mutagenic counterparts and phenothiazines. Differential absorption spectrophotometry revealed tight complex formation between these drugs and bacterial endotoxin or mitogens. All
Benz[c]acridine.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 32, 129-134 (1983-12-01)
T Kurihara et al.
Anticancer research, 14(5A), 1811-1822 (1994-09-01)
Resonance energies, circuit resonance energies and bond currents of benz[c]acridines were calculated by Aihara's IRE theory. Consequently, it was shown that these compounds had very stable aromatic characters with positive resonance energies and that the resonance energies per pi-electron values
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