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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Specific investigations: other studies

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Administrative data

Endpoint:
endocrine system modulation
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Reference
Reference Type:
publication
Title:
Potential estrogenic effects of phosphorus-containing flame retardants.
Author:
Zhang Q, Lu M, Dong X, Wang C, Zhang C, Liu W, Zhao M
Year:
2014
Bibliographic source:
Environ Sci Technol. 48(12), 6995-7001

Materials and methods

Principles of method if other than guideline:
The agonistic/antagonistic activity of a group of phosphorus-containing flame retardants (PFRs) is examined by three in vitro models (luciferase reporter gene assay, yeast two-hybrid assay, and E-screen assay). Molecule docking was used to further explain the interactions between ERα and PFRs.
Type of method:
in vitro

Test material

Constituent 1
Chemical structure
Reference substance name:
Tributyl phosphate
EC Number:
204-800-2
EC Name:
Tributyl phosphate
Cas Number:
126-73-8
Molecular formula:
C12H27O4P
IUPAC Name:
tributyl phosphate

Results and discussion

Details on results:
in the in vitro luciferase reporter gene assay no REC20 of Tributyl phosphate for ERα could be determined, i.e. no activity to E2. Only for potential estrogenic effects in the E-Screen assay absolute numbers were given (10-7 M for TBP and 10-9 M for E2).

Any other information on results incl. tables

The agonistic/antagonistic activity of a group of phosphorus-containing flame retardants (PFRs) is examined by three in vitro models (luciferase reporter gene assay, yeast two-hybrid assay, and E-screen assay). Molecular docking was used to further explain the interactions between ERα and PFRs. The authors state that TBP does not behave as an ERα agonist or antagonist. However in the E-Screen Assay a very low binding affinity occurred at 10-7 M. 

Applicant's summary and conclusion