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HCID 36934Erstellt: 31. Oktober 2026

1,2,7,8-Tetrachlorodibenzo-p-dioxin

2,3,6,7-TCDD · 1,2,7,8-TCDD · 1,2,7,8-Tetrachlorodibenzodioxin · 2,3,6,7-tetrachlorodibenzodioxin · 1,2,7,8-tetrachloro-dibenzo-p-dioxi · 1,2,7,8-Tetrachlorodibenzo[1,4]dioxin · 2,3,6,7-TETRACHLORODIBENZO-PARA-DIOXIN · 1,2,7,8-TETRACHLORODIBENZO-PARA-DIOXIN

https://huagongshe.com/de/chemical/36934

Molekülstruktur von 1,2,7,8-Tetrachlorodibenzo-p-dioxin

Identifikatoren & physikalische Daten

CAS No.34816-53-0
SummenformelC12H4Cl4O2
Durchschnittliche Molmasse322 g/mol
Monoisotopische Masse319,89654 g/mol
SMILESClc1cc2c(cc1Cl)Oc1c(ccc(Cl)c1Cl)O2
InChIKeyYDZCLBKUTXYYKS-UHFFFAOYSA-N
PubChem CID36934
ChEMBLCHEMBL137849
EC No.110-499-8
DTXSIDDTXSID3073478

Chemische & physikalische Eigenschaften

XLogP6
Polarare Oberfläche (TPSA)18,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen0
Schwere Atome18
Formalladung0
Komplexität316
LogP (Verteilungskoeffizient)6.38
Schmelzpunkt189.36°C (estimate)
Siedepunkt407.62°C (rough estimate)
Dichte1.6430 (estimate)
Brechungsindex1.6430 (estimate)
Henry-Konstante7.8×10-1 mol/(m3Pa) at 25℃, Wang and Wong (2002)
EPA chemische Informationen1,2,7,8-Tetrachlorodibenzo-p-dioxin (34816-53-0)

Sicherheit & Vorschriften

GHS-EinstufungWarningH302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Hazard Classes and CategoriesAcute Tox. 4 (100%)
Minimum Risk LevelAcute Oral: 0.0002 ug/kg/day (L134) Intermediate Oral: 0.00002 ug/kg/day (L134) Chronic Oral: 0.000001 ug/kg/day (L134)
TreatmentTreatment of CDD exposure may include washing the area of contact, GI decontamination, administering an IV, or forced alkaline diuresis. (L346)
Gesundheitliche AuswirkungenExposure to large amounts of CDDs causes chloracne, a severe skin disease with acne-like lesions that occur mainly on the face and upper body. CDDs may also cause liver damage and induce long-term alterations in glucose metabolism and subtle changes in hormonal levels. In addition, studies have shown that CDDs may disrupt the endocrine system and weaken the immune system, as well as cause reproductive damage and birth defects, central and peripheral nervous system pathology, thyroid disorders, endometriosis, and diabetes. (L177, L178)
ExpositionspfadeOral (L177)inhalation(L177)dermal (L177)
ToxizitätsübersichtCDDs cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the trascription of certain genes. The affinity for the Ah receptor depends on the structure of the specific CDD. The change in gene expression may result from the direct interaction of the Ah receptor and its heterodimer-forming partner, the aryl hydrocarbon receptor nuclear translocator, with gene regulatory elements or the initiation of a phosphorylation/dephosphorylation cascade that subsequently activates other transcription factors. The affected genes include several oncogenes, growth factors, receptors, hormones, and drug-metabolizing enzymes. The change in transcription/translation of these genes is believed to be the cause of most of the toxic effects of CDDs. (L177)
Signs and SymptomsIn addition to chloracne, CDD exposure causes skin rashes, discoloration, and excessive body hair. (L177)

Anwendungen & Verwendung

Verwenden

1,2,7,8-Tetrachlorodibenzo-p-dioxin is used as a standard in environmental testing and research into pesticides and impurities.

Carcinogen Classification3, not classifiable as to its carcinogenicity to humans. (L135)