50585-41-6 Usage
Description
2,3,7,8-TETRABROMODIBENZO-P-DIOXIN is a halogenated organic compound that belongs to the class of dibenzo-p-dioxins. It is characterized by the presence of four bromine atoms at the 2, 3, 7, and 8 positions on the dibenzo-p-dioxin molecule. 2,3,7,8-TETRABROMODIBENZO-P-DIOXIN has unique chemical and physical properties that make it suitable for specific applications in various fields.
Uses
Used in Environmental Analysis:
2,3,7,8-TETRABROMODIBENZO-P-DIOXIN is used as a reference compound in the development of analytical methods for the detection of polybrominated dibenzo-p-dioxins (PBDD/DF) in environmental samples. These methods are crucial for monitoring and assessing the presence of potentially harmful pollutants in the environment, as well as for regulatory purposes and ensuring compliance with environmental standards.
In this application, 2,3,7,8-TETRABROMODIBENZO-P-DIOXIN serves as a valuable tool for researchers and analysts, providing a means to accurately measure and quantify the levels of PBDD/DF in various environmental matrices, such as soil, water, and air. This information is essential for understanding the distribution, transport, and fate of these pollutants, as well as for developing strategies to mitigate their potential impacts on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 50585-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,8 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50585-41:
(7*5)+(6*0)+(5*5)+(4*8)+(3*5)+(2*4)+(1*1)=116
116 % 10 = 6
So 50585-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H4Br4O2/c13-5-1-9-10(2-6(5)14)18-12-4-8(16)7(15)3-11(12)17-9/h1-4H
50585-41-6Relevant articles and documents
ORDER OF THE REPLACEMENT OF HYDROGEN BY HALOGEN IN THE HALOGENATION OF DIBENZO-p-DIOXIN AND ITS NITRO AND AMINO DERIVATIVES
Kuntsevich, A. D.,Golovkov, V. F.,Chernov, S. A.
, p. 1279 - 1286 (2007/10/02)
The order of the replacement of hydrogen by halogen in the bromination and chlorination of dibenzo-p-dioxin and its nitro and amino derivatives was examined with the purpose of determining the possibilities of the formation of highly toxic isomers of halogenated dibenzo-p-dioxins from precursors with a tricyclic structure of dibenzo-p-dioxin.A number of halogenated dibenzo-p-dioxins were synthesized, which illustrates the order of the replacement, and their physicochemical and spectral characteristics are given.
FORMATION OF HETEROCYCLIC HAZARDOUS COMPOUNDS BY THERMAL DEGRADATION OF ORGANIC COMPOUNDS
Bieniek, Dieter,Bahadir, Muefit,Korte, Friedhelm
, p. 719 - 722 (2007/10/02)
2,3,7,8-Tetrabromodibenzofuran in ppm concentrations can be generated via reductive debromination and subsequent intramolecular cyclization during thermolysis of polybrominated aromatic compounds such as decabromodiphenyl ethers which are used as flame retardants in plastics.The respective tetrabromobenzodioxin isomer is produced in moderate amounts.In analogy to the chlorinated isomers the formation of toxic substances from incineration or fire accident constitutes a potential hazard.