InChI
1S/C20H12/c1-2-8-15-13(5-1)11-12-17-16-9-3-6-14-7-4-10-18(19(14)16)20(15)17/h1-12H
SMILES string
c1ccc2c-3c(ccc2c1)-c4cccc5cccc-3c45
InChI key
KHNYNFUTFKJLDD-UHFFFAOYSA-N
grade
certified reference material
agency
BCR®
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
cleaning products
cosmetics
environmental
food and beverages
personal care
pharmaceutical (small molecule)
format
neat
storage temp.
2-8°C
Analysis Note
For more information please see:
BCR049
BCR049
Legal Information
BCR is a registered trademark of European Commission
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
Etienne Bourgart et al.
Archives of toxicology, 93(8), 2165-2184 (2019-07-10)
Combined exposure to complex mixtures of polycyclic aromatic hydrocarbons (PAHs) and ultraviolet radiation (UVR) is suspected to enhance PAH skin permeability and skin cancer risk depending on PAH bioactivation. The impact of PAH mixtures (exposure dose, composition, and complexity) and
Carmela Lestingi et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(7), 1140-1152 (2017-05-18)
A gas-chromatographic single-quadrupole analytical method for the analysis of the 16 priority European Union (EU) polycyclic aromatic hydrocarbons (PAHs) in food is presented. The method fulfils the request of Regulation EU 836/2011 for an analytical procedure to be used for
B D Silverman et al.
Chemico-biological interactions, 47(3), 289-292 (1983-12-01)
The benzo- and dibenzofluoranthenes, widespread environmental contaminants, have been subjects of continued interest. Calculations of the reactivity of potential ultimate carcinogenic metabolites of the benzofluoranthenes predict unexpected behavior for these non-alternant hydrocarbons.
E J LaVoie et al.
Cancer letters, 70(1-2), 7-14 (1993-06-15)
Exceptional tumorigenic potency was observed with 4-fluorobenzo[j]fuoranthene (4-fluoroB[j]F) relative to benzo[j]fluoranthene (B[j]F) and 10-fluorobenzo[j]fluoranthene (10-fluoroB[j]F) in a mouse skin initiation promotion bioassay. Comparison of the tumorigenic response obtained at total initiating doses of 50, 100, and 1000 nmol firmly established
J L Autrup et al.
Chemico-biological interactions, 85(2-3), 141-150 (1992-12-01)
Formation of carcinogen-DNA adducts in rat oral epithelial cells after treatment with cigarette smoke condensate (CSC) or chewing tobacco in the presence of ethanol was investigated using the 32P-postlabeling procedure. Concomitant treatment of the cells with ethanol increased the relative
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