A polychlorinated dibenzodioxin
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin

Item No. 38597

Technical Information
Formal Name
1,2,3,4,6,7,8-heptachloro-dibenzo[b,e][1,4]dioxin
CAS Number
35822-46-9
Synonyms
  • 1,2,3,4,6,7,8-HpCDD
  • PCDD 73
  • Polychlorinated Dibenzodioxin 73
Molecular Formula
C12HCl7O2
Formula Weight
Purity
≥95%
Formulation
A solid
DMF: Slightly soluble upon heating
SMILES
ClC1=C(Cl)C=C2OC3=C(C(Cl)=C(C(Cl)=C3Cl)Cl)OC2=C1Cl
InChi Code
InChI=1S/C12HCl7O2/c13-2-1-3-10(7(17)4(2)14)21-12-9(19)6(16)5(15)8(18)11(12)20-3/h1H
InChi Key
WCLNVRQZUKYVAI-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Cayman Chemical
    Visit Our Environmental Toxicology Resource Center

    Explore additional resources to study natural toxins, pollutants including PFAS and 6-PPD-Q, and their biological effects.

    ENVIRONMENTAL TOXICOLOGY TOOLS & SERVICES
    Product Description

    1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin (1,2,3,4,6,7,8-HpCDD) is a polychlorinated dibenzodioxin (PCDD).1 It induces the expression of the genes encoding the cytochrome P450 (CYP) isoforms CYP1A1 and CYP1B1, as well as the aryl hydrocarbon receptor repressor (AhRR) in primary human peripheral blood lymphocytes and increases ethoxyresorufin-O-deethylase (EROD) activity, a marker of CYP1A1 activity, in isolated human peripheral blood lymphocytes in a concentration-dependent manner. 1,2,3,4,6,7,8-HpCDD (100 µg/kg) decreases the production of antibodies against sheep red blood cells in mice.2 Chronic administration of 1,2,3,4,6,7,8-HpCDD decreases the time to death and increases lung and liver tumorigenesis in rats.3 1,2,3,4,6,7,8-HpCDD has been found in freshwater fish, human breastmilk, and in the air near municipal waste incinerators.4,5,6

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. van Ede, K.I., Gaisch, K.P.J., van den Berg, M., et alDifferential relative effect potencies of some dioxin-like compounds in human peripheral blood lymphocytes and murine splenic cells. Toxicol. Lett. 226(1), 43-52 (2014).

    2. Kerkvliet, N.I., and Brauner, J.A. Mechanisms of 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin (HpCDD)-induced humoral immune suppression: Evidence of primary defect in T-cell regulation. Toxicol. Appl. Pharmacol. 87(1), 18-31 (1987).

    3. Rozman, K.K., Lebofsky, M., and Pinson, D.M. Chronic toxicity and carcinogenicity of 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin displays a distinct dose/time toxicity threshold (c x t = k) and a life-prolonging subthreshold effect. Food Chem. Toxicol. 43(5), 729-740 (2005).

    4. Zacharewski, T., Safe, L., Safe, S., et alComparative analysis of polychlorinated dibenzo-p-dioxin and dibenzofuran congeners in Great Lakes fish extracts by gas chromatography-mass spectrometry and in-vitro enzyme induction activities. Environ. Sci. Technol. 23(6), 730-735 (1989).

    5. Takekuma, M., Saito, K., Ogawa, M., et alLevels of PCDDs, PCDFs and Co-PCBs in human milk in Saitama, Japan, and epidemiological research. Chemosphere 54(1), 127-135 (2004).

    6. Hu, S.-W., ChangChien, G.-P., and Chan, C.-C. PCDD/Fs levels in indoor environments and blood of workers of three municipal waste incinerators in Taiwan. Chemosphere 55(4), 611-620 (2004).