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Toxicological information

Specific investigations: other studies

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Administrative data

Endpoint:
specific investigations: other studies
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: According to ECHA Practical Guide 6 the maximum score for read across is rel. 2

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Gene expression changes in the immature rat uterus: Effects of uterotrophic and sub-uterotrophic doses of bisphenol A
Author:
Ashby J, Odum J
Year:
2004
Bibliographic source:
Toxicological Sciences. 82(2): 458-467
Reference Type:
publication
Title:
The OECD program to validate the rat uterotrophic bioassay. phase 2: coded single-dose studies
Author:
Kanno J, Onyon L, Peddada S, Ashby J, Jacob E, Owens W
Year:
2003
Bibliographic source:
Environmental Health Perspectives. 111: 1550-1558
Reference Type:
publication
Title:
The OECD program to validate the rat uterotrophic bioassay. phase 2: dose-response studies
Author:
Kanno J, Onyon L, Peddada S, Ashby J, Jacob E, Owens W
Year:
2003
Bibliographic source:
Environmental Health Perspectives. 111: 1530-1549

Materials and methods

Test material

Reference
Name:
Unnamed
Type:
Constituent

Results and discussion

Any other information on results incl. tables

The substance contains approx. 15 % 2,2-bis(4-hydroxyphenyl)propane (CAS No 80-05-7), therefore data of 2,2-bis(4-hydroxyphenyl)propane are relevant for toxicological assessment and were thus included in the IUCLID.

Applicant's summary and conclusion