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1,3,7,8-Tetrachlorodibenzofuran, also known as 1,3,7,8-TETRACHLORODIPHENYLENEOXIDE, is a chemical compound belonging to the family of dibenzofurans. It is characterized by the presence of four chlorine atoms at the 1, 3, 7, and 8 positions, which contribute to its unique properties and applications.

57117-35-8

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57117-35-8 Usage

Uses

1. Environmental Testing and Research:
1,3,7,8-TETRACHLORODIPHENYLENEOXIDE is used as a standard for environmental testing and research. It is particularly useful in the study of waste incineration and its effects on persistent organic pollution in the environment. 1,3,7,8-TETRACHLORODIPHENYLENEOXIDE serves as a reference material to analyze and understand the presence and impact of similar toxic substances in the environment.
2. Industrial Applications:
In various industries, 1,3,7,8-TETRACHLORODIPHENYLENEOXIDE is used as an additive or intermediate in the production of chemicals and materials. Its specific application may vary depending on the industry's requirements and the compound's compatibility with other substances.
3. Analytical Chemistry:
1,3,7,8-TETRACHLORODIPHENYLENEOXIDE is also utilized in analytical chemistry as a reference compound for the development and validation of analytical methods and techniques. It helps researchers and analysts to ensure the accuracy and reliability of their measurements and results.
4. Toxicology Studies:
1,3,7,8-TETRACHLORODIPHENYLENEOXIDE is used in toxicology studies to investigate the effects of exposure to similar chlorinated dibenzofuran compounds on living organisms. This information is crucial for understanding the potential health risks associated with these chemicals and for developing strategies to mitigate their impact on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 57117-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,1 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57117-35:
(7*5)+(6*7)+(5*1)+(4*1)+(3*7)+(2*3)+(1*5)=118
118 % 10 = 8
So 57117-35-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H4Cl4O/c13-5-1-9(16)12-6-3-7(14)8(15)4-10(6)17-11(12)2-5/h1-4H

57117-35-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,7,8-tetrachlorodibenzofuran

1.2 Other means of identification

Product number -
Other names 1,3,7,8-TCDF

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57117-35-8 SDS

57117-35-8Downstream Products

57117-35-8Relevant academic research and scientific papers

Role of copper chloride in the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans during incineration

Hatanaka, Takeshi,Kitajima, Akio,Takeuchi, Masao

, p. 73 - 79 (2007/10/03)

Combustion experiments in a laboratory-scale fluidized-bed reactor were performed to elucidate the role of copper chloride in formation of polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) during model waste incineration. The amounts of PCDDs and PCDFs formed, the homologue profiles, and the isomer distributions were measured in the flue gas from incineration of model wastes containing various levels of copper. A correlation was found between the Cu content of the waste and the proportion of each congener. An increase in copper enhanced the formation of certain congeners, showing that copper acts as a catalyst for formation of PCDDs and PCDFs. An increase in the copper content of the waste decreased the CO concentration in the flue gas and reduced the formation of PCDDs and PCDFs during incineration. This indicates that copper also works as an oxidation catalyst to promote combustion, leading to lower concentrations of products of incomplete combustion. It is indispensable to consider both roles of the catalyst, i.e., enhancement and suppression, in the formation of PCDDs and PCDFs during waste incineration, which are estimated separately from the isomer distributions and the amounts of PCDDs and PCDFs formed.

Isomer distributions of polychlorinated dibenzo-p-dioxins/dibenzofurans formed during de novo synthesis on incinerator fly ash

Addink, Ruud,Govers, Harrie A. J.,Olie, Kees

, p. 1888 - 1893 (2007/10/03)

Polychlorinated dibenzo-p-dioxins (PCDD) and dibenzofurans (PCDF) emitted from municipal waste incinerators appear to have a chlorination pattern that is quite constant across various samples and conditions. This suggested that these patterns may be controlled by thermodynamic properties of the individual PCDD/F congeners, such as the free Gibbs energy of formation (Δg°(f,T)). This would make prediction of the isomer composition of a particular sample (and hence its TEQ value) possible, based on values of ΔG°(f,T). A laboratory scale study was carried out with activated carbon on fly ash as the source of PCDD/F formation. Although it was found that the isomer distributions within homologues were independent of the reaction time (proof of thermodynamic control), other observations (lack of equilibrium/isomerization between isomers and lack of similarity between isomer distributions measured and predicted by ΔG°(f,T)) contradicted the possibility of thermodynamic control. Hence, this study could not confirm that de novo formation of PCDD/F could explain thermodynamically controlled isomer distributions in incinerators. Some recommendations for further work- time-based studies with precursors, isomerization studies with single congeners, and more data on ΔG°(f,T) values of PCDD/F-were made. Polychlorinated dibenzo-p-dioxins (PCDD) and dibenzofurans (PCDF) emitted from municipal waste incinerators appear to have a chlorination pattern that is quite constant across various samples and conditions. This suggested that these patterns may be controlled by thermodynamic properties of the individual PCDD/F congeners, such as the free Gibbs energy of formation (ΔG°f,T). This would make prediction of the isomer composition of a particular sample (and hence its TEQ value) possible, based on values of ΔG°f,T. A laboratory scale study was carried out with activated carbon on fly ash as the source of PCDD/F formation. Although it was found that the isomer distributions within homologues were independent of the reaction time (proof of thermodynamic control), other observations (lack of equilibrium/isomerization between isomers and lack of similarity between isomer distributions measured and predicted by ΔG°f,T) contradicted the possibility of thermodynamic control. Hence, this study could not confirm that de novo formation of PCDD/F could explain thermodynamically controlled isomer distributions in incinerators. Some recommendations for further work - time-based studies with precursors, isomerization studies with single congeners, and more data on ΔG°f,T values of PCDD/F - were made.

Synthesis of the 38 Tetrachlorodibenzofuran Isomers and Identification by Capillary Column Gas Chromatography/Mass Spectrometry

Mazer, Thomas,Hileman, Fred D.,Noble, Roy W.,Brooks, Joseph J.

, p. 104 - 110 (2007/10/02)

The 38 positional isomers of tetrachlorodibenzofuran have been synthesized by pyrolysis of specific polychlorinated biphenyl congeners, ultraviolet photolysis of pentachlorodibenzofurans, and chlorination of trichlorodibenzofurans by aromatic substitution.The specificity of these reactions in combinatiuon with capillary column gas chromatography with mass spectrometric detection has allowed each of these isomers to be identified based on their relative elution order.

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