60390-27-4

Basic information

• Product Name: 2,6-DICHLORODIBENZOFURAN
• Synonyms: 2,6-DICHLORODIBENZOFURAN
• CAS NO: 60390-27-4
• Molecular Formula: C12H6Cl2O
• Molecular Weight: 237.08
• Mol File: 60390-27-4.mol

Chemical Properties

• Boiling Point: 356.4°Cat760mmHg
• Flash Point: 169.3°C
• Appearance: /
• Density: 1.442g/cm³
• Vapor Pressure: 6.02E-05mmHg at 25°C
• Refractive Index: 1.707
• CAS DataBase Reference: 2,6-DICHLORODIBENZOFURAN(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DICHLORODIBENZOFURAN(60390-27-4)
• EPA Substance Registry System: 2,6-DICHLORODIBENZOFURAN(60390-27-4)

Safety Data

• Hazardous Substances Data: 60390-27-4(Hazardous Substances Data)

Usage

Uses

Used in Environmental Testing and Research:
2,6-Dichlorodibenzofuran is used as a standard in environmental testing and research applications. It serves as a reference compound for the study of the thermal decomposition of endosulfan and the resulting formation of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs), which are environmental toxins. This helps in understanding the environmental impact and potential risks associated with the presence of these toxic compounds.

InChI:InChI=1/C12H6Cl2O/c13-7-4-5-11-9(6-7)8-2-1-3-10(14)12(8)15-11/h1-6H

Upstream product

• 87-86-5 Pentachlorophenol 
• 87-65-0 2,6-Dichlorophenol 
• 933-75-5 2,3,6-trichlorophenol 
• 95-57-8 2-monochlorophenol 
• 106-48-9 4-chloro-phenol 
• 108-95-2 phenol 
• 56966-48-4 5-chloro-2-(2-chloro-phenoxy)-aniline 

Relevant articles and documents

Prediction of polychlorinated dibenzofuran congener distribution from gas-phase phenol condensation pathways

A model for predicting the distribution of dibenzofuran and polychlorinated dibenzofuran (PCDF) congeners from a distribution of phenols was developed. The model is based on a simplified chemical mechanism. Relative rate constants and reaction order with respect to phenol precursors were derived from experimental results using single phenols and equal molar mixtures of up to four phenols. For validation, experiments were performed at three temperatures using a distribution of phenol and 19 chlorinated phenols as measured in municipal waste incinerator exhaust gas. Comparison of experimental measurements and model predictions for PCDF isomer distributions and homologue pattern shows agreement within measurement uncertainty. The R-squared correlation coefficient exceeds 0.9 for all PCDF isomer distributions and the distribution of PCDF homologues. These results demonstrate that the distribution of dibenzofuran and the 135 PCDF congeners from gas-phase condensation of phenol and chlorinated phenols can be predicted from measurement of the distribution of phenol and the 19 chlorinated phenol congeners.

Identification of surrogate compounds for the emission of PCDD/F (I-TEQ value) and evaluation of their on-line realtime detectability in flue gases of waste incineration plants by REMPI-TOFMS mass spectrometry

Correlations between products of incomplete combustion (PIC), e.g., chloroaromatic compounds, can be used to characterise the emissions from combustion processes, like municipal or hazardous waste incineration. A possible application of such relationships may be the on-line real-time monitoring of a characteristic surrogate, e.g., with Resonance-Enhanced Multiphoton Ionization-Time-of-Flight Mass Spectrometry (REMPI-TOFMS). In this paper, we report the relationships of homologues and individual congeners of chlorinated benzenes (PCBz), dibenzo-p-dioxins (PCDD), dibenzofurans (PCDF) and phenols (PCPh) to the International Toxicity Equivalent (I-TEQ) of the PCDD/F (I-TEQ value) in the flue gas and stack gas of a 22 MW hazardous waste incinerator (HWI). As the REMPI detection sensitivity is decreasing with the increase of the degree of chlorination, this study focuses on the lower chlorinated species of the compounds mentioned above. Lower chlorinated species, e.g., chlorobenzene (MCBz), 1,4-dichlorobenzene, 2,4,6-trichlorodibenzofuran or 2,4-dichlorophenol, were identified as I-TEQ surrogates in the flue gas. In contrast to the higher chlorinated phenols, the lower chlorinated phenols (degree of chlorination 4) were not reliable as surrogates in the stack gas. The identified surrogates are evaluated in terms of their detectability by REMPI-TOFMS laser mass spectrometry. The outcome is that MCBz is the best suited surrogate for (indirect) on-line measuring of the I-TEQ value in the flue gas by REMPI-TOFMS. The correlation coefficient r of the MCBz concentration to the I-TEQ in the flue gas was 0.85.