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386332

Sigma-Aldrich

7,9-Dimethylbenz[c]acridine

technical grade

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About This Item

Empirical Formula (Hill Notation):
C19H15N
CAS Number:
963-89-3
Molecular Weight:
257.33
MDL number:
MFCD00192074
UNSPSC Code:
12352100
PubChem Substance ID:
24864082
NACRES:
NA.22

grade

technical grade

bp

300 °C/10 mmHg (lit.)

mp

157-161 °C (lit.)

SMILES string

Cc1ccc2nc3c(ccc4ccccc34)c(C)c2c1

InChI

1S/C19H15N/c1-12-7-10-18-17(11-12)13(2)15-9-8-14-5-3-4-6-16(14)19(15)20-18/h3-11H,1-2H3

InChI key

HEFJMRLDXHSXEP-UHFFFAOYSA-N

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
09012LY

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Y Ye et al.
Carcinogenesis, 16(4), 787-793 (1995-04-01)
The major and minor metabolites of the potent polycyclic aza-aromatic carcinogens 7,9-dimethylbenz[c]acridine and 7,10-dimethylbenz[c]acridine, and the stereochemistry of the dihydrodiol metabolites have been previously described. The metabolite distributions produced in incubations of the aza-aromatic compounds with liver microsomes from phenobarbital-
Effects of several dimethylbenzacridines on secondary hamster embryo cells: neoplastic transformation.
D Papadopoulo et al.
European journal of cancer, 17(2), 179-186 (1981-02-01)
Y Ye et al.
Chemical research in toxicology, 8(2), 188-202 (1995-03-01)
The hepatic microsomal metabolites of the highly carcinogenic dimethylbenzacridines, 7,9-dimethylbenz[c]acridine (7,9-DMBAC), and 7,10-dimethylbenz[c]acridine (7,10-DMBAC) were obtained with preparations from 3-methylcholanthrene-pretreated rats. Metabolites were separated by reversed-phase HPLC and characterized using UV spectral data and chemical ionization-mass spectrometry after trimethylsilylation and
Y Ye et al.
Chemical research in toxicology, 8(2), 203-208 (1995-03-01)
The monofunctionalized dihydrodiol metabolites of 7,9-dimethylbenz[c]acridine and 7,10-dimethylbenz[c]acridine formed in incubations with rat liver microsomes from untreated and phenobarbital and 3-methylcholanthrene-pretreated rats were isolated by reversed-phase high performance liquid chromatography. The relative amounts of each enantiomer were determined by HPLC

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