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等级
certified reference material
TraceCERT®
质量水平
产品线
TraceCERT®
CofA
current certificate can be downloaded
包装
ampule of 1 mL
浓度
2000 μg/mL in dichloromethane
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
cleaning products
cosmetics
environmental
food and beverages
personal care
包装形式
single component solution
储存温度
2-30°C
SMILES字符串
c21c3c4c(c2ccc5c1cccc5)cccc4ccc3
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
一般描述
Benzo[j]fluoranthene is a polycyclic aromatic hydrocarbon, which is carcinogenic in nature and can be generated into the environment via combustion of coal, coal tar and petroleum products.
应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
其他说明
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
法律信息
TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险分类
Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Central nervous system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
其他客户在看
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A Comprehensive Guide to the Hazardous Properties of Chemical Substances (2007)
Report on Carcinogens (12th Ed. ) (2011)
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.
J E Rice et al.
Cancer research, 47(23), 6166-6170 (1987-12-01)
The metabolism of benzo[j]fluoranthene (BjF) in vivo in mouse skin was investigated. trans-4,5-Dihydro-4,5-dihydroxybenzo[j]fluoranthene (BjF-4,5-diol) and trans-9,10-dihydro-9,10-dihydroxybenzo[j]fluoranthene (BjF-9,10-diol) have been identified as major metabolites. In addition, 4- and 10-hydroxybenzo[j]fluoranthene and benzo[j]fluoranthen-4,5-dione have been tentatively identified among the metabolites formed in vivo
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
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