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HCID 38439Erstellt: 1. November 2026

1,2,3,7,8-Pentachlorodibenzo-p-dioxin

1,2,3,7,8-PCDD · 1,2,3,7,8-PNCDD · 1,2,3,7,8-PECDD · 1,2,3,7,8-Pentachlorooxanthrene · 1,2,3,7,8-PENTACHLORODIBENZODIOXIN · Pentachlorobenzo-p-dioxin, 1,2,3,7,8- · 1,2,3,7,8-pentachloro-dibenzo-p-dioxi · 2,3,4,7,8-Pentachlorodibenzo[1,4]dioxin

https://huagongshe.com/de/chemical/38439

Molekülstruktur von 1,2,3,7,8-Pentachlorodibenzo-p-dioxin

Identifikatoren & physikalische Daten

CAS No.40321-76-4
SummenformelC12H3Cl5O2
Durchschnittliche Molmasse356,4 g/mol
Monoisotopische Masse353,857568 g/mol
SMILESClc1cc2c(cc1Cl)Oc1c(cc(Cl)c(Cl)c1Cl)O2
InChIKeyFSPZPQQWDODWAU-UHFFFAOYSA-N
PubChem CID38439
ChEMBLCHEMBL137220
ChEBICHEBI:81501
EC No.694-814-9
DTXSIDDTXSID7052078

Chemische & physikalische Eigenschaften

XLogP6,6
Polarare Oberfläche (TPSA)18,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren2
Frei drehbare Bindungen0
Schwere Atome19
Formalladung0
Komplexität344
SpringerMaterials PropertiesBoiling point
LogP (Verteilungskoeffizient)6.64
Endocrine DisruptorsPotential endocrine disrupting compound
Collision Cross Section165.2 Ų [M]+ [CCS Type: TIMS, Method: calibration with PAHs]
Schmelzpunkt206°C (estimate)
Siedepunkt442.63°C (rough estimate)
Dichte1.7800 (estimate)
Brechungsindex1.6610 (estimate)
Löslichkeitn-nonane: Soluble
Henry-Konstante5.2×10-5 mol/(m3Pa) at 25℃, Paasivirta et al. (1999)
EPA chemische Informationen1,2,3,7,8-Pentachlorodibenzo-p-dioxin (40321-76-4)

Sicherheit & Vorschriften

GHS-EinstufungDangerH300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]P264, P270, P273, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Regulatorische InformationenHazard Traits - BioaccumulationCarcinogenicityDermatotoxicityEndocrine ToxicityEnvironmental PersistenceEnvironmental toxHematotoxicityHepatotoxicity and Digestive System ToxicityReproductive ToxicityRespiratory ToxicityRegulation (EC) No 178/2002 (amended)
Hazard Classes and CategoriesAcute Tox. 1 (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)
Protective Action Criteria (PAC)0.00013 [mg/m3]0.0014 [mg/m3]0.0085 [mg/m3]
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)

Anwendungen & Verwendung

Verwenden

A toxic polychlorinated dibenzo-p-dioxin detected in domestic meat and poultry.

Toxizitätsübersicht
CDDs cause their toxic effects by binding to the aryl hydrocarbon receptor and subsequently altering the transcription 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)
Carcinogen Classification3, not classifiable as to its carcinogenicity to humans. (L135)
RAIS Toxicity Values38WHO/TEF4e-087e-10
UN-Transportnummer2811
ToxizitätLD50 orl-rat: 206 mg/kg ARTODN 66,471,92
Gefahrenklasse6.1(a)
VerpackungsgruppeI