A55403
3-Aminofluoranthene
90%
Synonym(s):
3-Fluoranthenamine
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About This Item
Empirical Formula (Hill Notation):
C16H11N
CAS Number:
Molecular Weight:
217.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
assay
90%
mp
115-117 °C (lit.)
SMILES string
Nc1ccc2-c3ccccc3-c4cccc1c24
InChI
1S/C16H11N/c17-15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H,17H2
InChI key
VHGJAFIHUSTRGB-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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D L Berry et al.
Carcinogenesis, 6(10), 1403-1407 (1985-10-01)
1-Nitropyrene (1-NO2Py), 3-nitrofluoranthene (3-NO2Ft), 3-aminofluoranthene (3-NH2Ft) and 8-nitrofluoranthene (8-NO2Ft) were tested for mutagenicity in cultured Chinese hamster V79 cells. Mutations at the hypoxanthine-guanine phosphoribosyl transferase (HGPRT) gene locus were quantified. 1-NO2Py had marginal direct-acting mutagenicity which was enhanced by a
M A Belisario et al.
Toxicology, 108(1-2), 101-108 (1996-04-15)
Nitroarenes are environmental contaminants produced during incomplete combustion processes. Nitroreduction, the most important pathway of nitroarene toxification, occurs mainly in the liver and intestine. In the present study, we show that human red cells may also possess the metabolic competence
Nana Asare et al.
Toxicology, 255(3), 140-150 (2008-12-02)
In this study, we show that the environmental pollutant, 3-nitrofluoranthene (3-NF) but not its amine form, 3-aminofluoranthene (3-AF), induces apoptosis as well as regulated necrosis with necroptotic features in Hepa1c1c7 cells. Upon exposure to 3-NF, both typical apoptotic and necrotic
Claudia Dietze et al.
Analytical and bioanalytical chemistry, 407(29), 8735-8743 (2015-09-24)
A fast and straightforward method to prototype microfluidic chip systems for dead-volume-free hyphenation to electrospray-ionisation mass spectrometry is presented. The developed approach based on liquid-phase lithography provides an inexpensive and reliable access to microfluidic chips for MS coupling which can
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