1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN
1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN Basic information
- Product Name:
- 1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN
- Synonyms:
-
- e)(1,4)dioxin,1,2,3,6,7,8-hexachloro-dibenzo(
- nci-c03703
- 1,2,3,6,7,8-hexachlorodibenzodioxin
- 1,2,3,6,7,8-HCDD
- Hexachlorodibenzo-p-dioxin, 1,2,3,6,7,8-
- 1,2,3,6,7,8-Hexachlorodibenzo[b,e][1,4]dioxin
- D-67
- HxCDD
- CAS:
- 57653-85-7
- MF:
- C12H2Cl6O2
- MW:
- 390.86
- Product Categories:
-
- Aromatics
- Heterocycles
- Mol File:
- 57653-85-7.mol
1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN Chemical Properties
- Melting point:
- 285°C
- Boiling point:
- 475.35°C (rough estimate)
- Density
- 1.8350 (estimate)
- refractive index
- 1.6710 (estimate)
- solubility
- nonane:toluene (8:2): soluble
- EPA Substance Registry System
- 1,2,3,6,7,8-Hexachlorodibenzo-p-dioxin (57653-85-7)
Safety Information
- RIDADR
- 2811
- HazardClass
- 6.1(a)
- PackingGroup
- I
- Hazardous Substances Data
- 57653-85-7(Hazardous Substances Data)
1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN Usage And Synthesis
Uses
A toxic polychlorinated dibenzo-p-dioxin detected in domestic meat and poultry.
Definition
ChEBI: 1,2,3,6,7,8-Hexachlorodibenzodioxin is a polychlorinated dibenzodioxine.
General Description
Fluffy white solid.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN is the type of compound that is extremely stable, even on heating to 1292° F. Solutions of 1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN may be sensitive to light. Solutions of this type of compound in methanol are degraded by exposure to summer sunlight or irradiation with an ultraviolet lamp (300 nm).
Fire Hazard
Flash point data for 1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN are not available; however, 1,2,3,6,7,8-HEXACHLORODIBENZO-P-DIOXIN is probably combustible.
References
[1] TINGTING XU. A rapid and reagent-free bioassay for the detection of dioxin-like compounds and other aryl hydrocarbon receptor (AhR) agonists using autobioluminescent yeast[J]. Analytical and Bioanalytical Chemistry, 2017, 410 4: 1247-1256. DOI: 10.1007/s00216-017-0780-1
[2] M P HOLSAPPLE. Suppression of humoral antibody production by exposure to 1,2,3,6,7,8-hexachlorodibenzo-p-dioxin.[J]. Journal of Pharmacology and Experimental Therapeutics, 1984, 231 3: 518-526.
[3] M. PAJUREK S. M M Warenik Bany. Feed as a source of dioxins and PCBs[J]. Chemosphere, 2022, 308: Article 136243. DOI: 10.1016/j.chemosphere.2022.136243
[4] SUH-WOAN HU Chang C C Guo Ping ChangChien. PCDD/Fs levels in indoor environments and blood of workers of three municipal waste incinerators in Taiwan[J]. Chemosphere, 2004, 55 4: Pages 611-620. DOI: 10.1016/j.chemosphere.2003.10.057
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