2,3,7,8-Tetrachlorodibenzodioxin (BioCAD00000002965)

blood

Metabolite Card

Formula: C12H4Cl4O2 (319.8965)
SMILES: [H]C1=C2OC3=C([H])C(Cl)=C(Cl)C([H])=C3OC2=C([H])C(Cl)=C1Cl

Synonyms [en]

2,3,7,8-Tetrachlorodibenzodioxin; TCDD; 2,3,7,8-Tetrachlorodibenzo-p-dioxin; PCDD 48; Tetrachlorodibenzodioxin; Dioxine

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

2,3,7,8-Tetrachlorodibenzodioxin. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000002965). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

2,3,7,8-tetrachlorodibenzo-p-dioxin (tcdd) appears as white crystals or tan crystalline powder. (NTP, 1992) 2,3,7,8-tetrachlorodibenzodioxine is a polychlorinated dibenzodioxine. 2,3,7,8-Tetrachlorodibenzo-p-dioxin . 2,3,7,8-Tetrachlorodibenzo-P-dioxin is 2,3,7,8-Tetrachlorodibenzo-p-dioxin which is often referred to simply as dioxin and is the reference for a number of compounds which are similar structurally and have dioxin-like toxicity. A substance extremely toxic to mammals, with a wide variation in sensitivity among species. Longer-term exposure of test mammals to lesser amounts can affect reproduction, cause birth defects, damage the liver and suppress the immune system. Several studies suggest that exposure to TCDD increases the risk of several types of cancer in people. Animal studies have also shown an increased risk of cancer from exposure to TCDD. The WHO and the USA DHHS have determined that TCDD is a human carcinogen. (NCI) 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) can cause cancer according to an independent committee of scientific and health experts. It can cause developmental toxicity according to The Environmental Protection Agency (EPA). 2,3,7,8-Tetrachlorodibenzo-p-dioxin is the most toxic of 75 chlorinated dibenzo-p-dioxin (CDD) congeners. CDDs are a class of manufactured chemicals that consist of dioxin skeletel structures with chlorine substituents. They are also persistent organic pollutants (POPs), thus their production is regulated in most areas. Dioxins occur as by-products from the manufacture of organochlorides, the bleaching of paper, chlorination by waste and drinking water treatment plants, municipal solid waste and industrial incinerators, and natural sources such as volcanoes and forest fires. (L177, L178) Dibenzodioxin derivatives that contain multiple chloride atoms bound to the benzene ring structures.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 1746-01-6
  • PubChem: 15625
  • ChEBI: ChEBI:28119
  • HMDB: HMDB0258755
  • KEGG: C07557
  • NCBI MeSH: Polychlorinated Dibenzodioxins
  • Wikipedia: 2,3,7,8-Tetrachlorodibenzo-P-Dioxin
  • Wikipedia: 2,3,7,8-Tetrachlorodibenzodioxin
  • Wikipedia: 2\,3\,7\,8-Tetrachlorodibenzo-P-Dioxin
  • Metlin: METLIN_66680

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
Reactome:R-BTA-1430728 Metabolism
Reactome:R-BTA-211945 Phase I - Functionalization of compounds
Reactome:R-BTA-211981 Xenobiotics
Reactome:R-CEL-211859 Biological oxidations
Reactome:R-CEL-8937144 Aryl hydrocarbon receptor signalling
Reactome:R-CFA-1430728 Metabolism
Reactome:R-CFA-211976 Endogenous sterols
Reactome:R-DME-8937144 Aryl hydrocarbon receptor signalling
Reactome:R-GGA-211976 Endogenous sterols
Reactome:R-HSA-400206 Regulation of lipid metabolism by PPARalpha
Reactome:R-HSA-211859 Biological oxidations
Reactome:R-MMU-1430728 Metabolism
Reactome:R-MMU-211859 Biological oxidations
Reactome:R-RNO-211945 Phase I - Functionalization of compounds
Reactome:R-RNO-211981 Xenobiotics
Reactome:R-SSC-211945 Phase I - Functionalization of compounds
Reactome:R-SSC-211981 Xenobiotics
Reactome:R-XTR-8937144 Aryl hydrocarbon receptor signalling
Reactome:R-BTA-211859 Biological oxidations
Reactome:R-CFA-211897 Cytochrome P450 - arranged by substrate type
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