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64126-87-0

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64126-87-0 Usage

Description

1,2,4,8-TCDF, also known as Tetrachlorodibenzofuran, is a chlorinated organic compound that belongs to the family of dibenzofuran derivatives. It is characterized by the presence of four chlorine atoms at the 1, 2, 4, and 8 positions, which contribute to its chemical properties and potential applications.

Uses

Used in Environmental Testing and Research:
1,2,4,8-TCDF is used as a standard compound in environmental testing and research for the detection and quantification of dioxin-like compounds. Its presence in samples can help identify contamination levels and assess the environmental impact of these toxic substances.
Used in Dioxin Formation Studies:
1,2,4,8-TCDF is also used as a model compound in the study of dioxin formation due to pesticide exposure to light. By understanding the chemical reactions and pathways involved in the formation of dioxins, researchers can develop strategies to minimize their production and reduce their environmental and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 64126-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,2 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64126-87:
(7*6)+(6*4)+(5*1)+(4*2)+(3*6)+(2*8)+(1*7)=120
120 % 10 = 0
So 64126-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H4Cl4O/c13-5-1-2-9-6(3-5)10-11(16)7(14)4-8(15)12(10)17-9/h1-4H

64126-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,8-tetrachlorodibenzofuran

1.2 Other means of identification

Product number -
Other names Dibenzofuran,1,2,4,8-tetrachloro

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:64126-87-0 SDS

64126-87-0Downstream Products

64126-87-0Relevant articles and documents

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.

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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