A47052
6-Aminochrysene
95%
Synonym(s):
6-Chrysenamine
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About This Item
Empirical Formula (Hill Notation):
C18H13N
CAS Number:
Molecular Weight:
243.30
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-149-7
MDL number:
Assay:
95%
Form:
solid
InChI key
KIVUHCNVDWYUNP-UHFFFAOYSA-N
InChI
1S/C18H13N/c19-18-11-17-13-6-2-1-5-12(13)9-10-15(17)14-7-3-4-8-16(14)18/h1-11H,19H2
SMILES string
Nc1cc2c3ccccc3ccc2c4ccccc14
assay
95%
form
solid
mp
209-211 °C (lit.)
Quality Level
Related Categories
Application
Produces tumors in mice.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Yi Zhang et al.
Environmental toxicology and chemistry, 25(7), 1920-1925 (2006-07-13)
Chrysene is one of the basic polycyclic aromatic hydrocarbons that are toxic environmental pollutants. The photoproducts of 6-aminochrysene (6AC) include 5,6-chrysenequinone (5,6-CQ) along with some minor products. In this study, cytotoxicity and genotoxicity of 6AC and 5,6-CQ to a human
S M Morris et al.
Mutation research, 310(1), 45-54 (1994-10-01)
Cells from the human lymphoblastoid cell line, AHH-1, were exposed to two direct-acting mutagens, ethyl methanesulfonate (EMS) and ethyl nitrosourea (ENU), and to three carcinogens that require metabolic activation to an electrophile, benzo[a]pyrene (B(a)P), 6-aminochrysene (6-AC), and 6-nitrochrysene (6-NC); mutation
S Lahmy et al.
Toxicology, 29(4), 345-356 (1984-02-01)
By microspectrofluorimetry on single living cells (murine fibroblasts 3T3), we have obtained monoexponential decreases of fluorescence intensity for benzo[a]pyrene (B[a]P) and 6-aminochrysene (6a-chrysene) metabolism. These kinetics are characteristics of B[a]P and 6a-chrysene metabolism and histograms can be drawn from the
H Yamazaki et al.
Carcinogenesis, 14(7), 1271-1278 (1993-07-01)
We reported previously that the potent mutagen 6-aminochrysene is catalyzed principally by rat liver microsomal P4501A and P4502B enzymes to reactive metabolites that induce umu gene expression in O-acetyltransferase-over-expressing strain Salmonella typhimurium NM2009; the proposal was made that there are
S Lahmy et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 35(2), 197-201 (1987-02-01)
The purpose of this study was to determine if dibenzo(c,h)acridine could be used as a probe for the N-heterocyclic aromatic compound detoxification system. The determination was achieved by cell population studies (histograms) using microspectrofluorimetry on single living cells. The results
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