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Merck
CN

BCR049

苯并[j]荧蒽

BCR®, certified reference material

别名:

苯并[j]荧蒽(纯度)

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关于此项目

经验公式(希尔记法):
C20H12
化学文摘社编号:
分子量:
252.31
UNSPSC Code:
41116107
PubChem Substance ID:
MDL number:
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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

SMILES string

c1ccc2c-3c(ccc2c1)-c4cccc5cccc-3c45

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

InChI key

KHNYNFUTFKJLDD-UHFFFAOYSA-N

Analysis Note

For more information please see:
BCR049

Legal Information

BCR is a registered trademark of European Commission


pictograms

Health hazardEnvironment

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



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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
Miyuki Fukai et al.
Journal of natural products, 75(1), 22-25 (2011-12-14)
Four novel benzo[j]fluoranthene derivatives, hypoxylonols C (3), D (4), E (5), and F (6), have been isolated from the mushroom Hypoxylon truncatum, together with two known benzo[j]fluoranthene derivatives, hypoxylonols A (1) and B (2). The structures were established by analysis