tris(4-chlorophenyl)methanol

Synonyms: "tris(4-chlorophenyl)methanol", "4,4',4''-trichlorotrityl alcohol", "tri(4-chlorophenyl)methanol", "tris-(4-chloro-phenyl)-methanol", "tris(p-chlorophenyl) carbinol", "tris-(p-chlorophenyl) methanol", "tris(4-chlorophenyl)methan-1-ol".

Source: tris(4-chlorophenyl)methanol is an environmental pollutant commonly found in animal tissues.

Identifiers:

IUPAC Name: tris(4-chlorophenyl)methanol
CAS Number: 3010-80-8
PubChem ID: 76379
InChiKey: BPFKTJMHOWDJKI-UHFFFAOYSA-N
Canonical SMILES: C1=CC(=CC=C1C(C2=CC=C(C=C2)Cl)(C3=CC=C(C=C3)Cl)O)Cl

Structural Properties:

Molecular Formula: C₁₉H₁₃Cl₃O
Molecular Weight: 363.662

Pharmacophore Features:

Number of bond donors: 1
Number of bond acceptors: 1
Number of atoms different from hydrogen: 23

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Korner W, Vinggaard AM, Terouanne B, Ma R, Wieloch C, Schlumpf M, Sultan C, Soto AM. 2004. Interlaboratory comparison of four in vitro assays for assessing androgenic and antiandrogenic activity of environmental chemicals. Environ Health Perspect 112(6):695-702. URL: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1241964/.
Lascombe I, Beffa D, Ruegg U, Tarradellas J, Wahli W. 2000. Estrogenic activity assessment of environmental chemicals using in vitro assays: Identification of two new estrogenic compounds. Environ Health Perspect 108(7):621-629. DOI: 10.2307/3434882 . URL: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1638169/.
Poon R, Lecavalier P, Bergman A, Yagminas A, Chu I, Valli VE. 1997. Effects of tris(4-chlorophenyl)methanol on the rat following short-term oral exposure. Chemosphere 34(1):1-12. DOI: 10.1016/S0045-6535(96)00363-3. URL: https://www.sciencedirect.com/science/article/pii/S0045653596003633.