推荐产品
等级
certified reference material
Agency
BCR®
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
cleaning products
cosmetics
environmental
food and beverages
personal care
pharmaceutical (small molecule)
包装形式
neat
储存温度
2-8°C
SMILES字符串
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
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分析说明
For more information please see:
BCR049
BCR049
法律信息
BCR is a registered trademark of European Commission
警示用语:
Danger
危险声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
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
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
Chemico-biological interactions, 84(1), 37-53 (1992-09-14)
The metabolism and mutagenic activity of 4-fluorobenzo[j]fluoranthene (4F-B[j]F) and 10-fluorobenzo[j]fluoranthene (10F-B[j]F) were evaluated and compared with benzo[j]fluoranthene (B[j]F) using an identical rat liver homogenate preparation. Previous studies have shown that the major genotoxic metabolites of B[j]F are the 4,5- and
Cancer research, 54(4), 962-968 (1994-02-15)
Benzo[j]fluoranthene (B[j]F), trans-4,5-dihydro-4,5-dihydroxy-B[j]F, and trans-9,10-dihydro-9,10-dihydroxy-B[j]F were evaluated for tumorigenic activity in newborn CD1 mice. These dihydrodiols were assayed at doses of 1.10 and 0.275 mumol/mouse. B[j]F and the syn- and anti-diol epoxides derived from these dihydrodiols were evaluated at doses
Journal of chromatography. A, 867(1-2), 93-104 (2000-02-12)
This article describes a detector for liquid chromatography that provides three-dimensional, excitation-emission-intensity data of fluorescent compounds. The instrument achieves multi-wavelength excitation by employing a polychromator that disperses radiation along the vertical portion of a quartz capillary flow cell. The ensuing
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