Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
(Q)SAR
Adequacy of study:
disregarded due to major methodological deficiencies
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: The study results are disregarded as the substance is out of the the Applicability Domain (AD) of the model.
Justification for type of information:
QSAR prediction: migrated from IUCLID 5.6

Data source

Reference
Reference Type:
publication
Title:
Predicted Oral rat LD50
Author:
U.S. Environmental Protection
Bibliographic source:
T.E.S.T. v.4.1
Report date:
2013

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: General model for estimating the LD50
Principles of method if other than guideline:
no data
GLP compliance:
no
Test type:
other: QSAR
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-benzylidenephthalide
EC Number:
209-388-8
EC Name:
3-benzylidenephthalide
Cas Number:
575-61-1
Molecular formula:
C15H10O2
IUPAC Name:
3-benzylidene-2-benzofuran-1-one
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder

Administration / exposure

Control animals:
no

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
ca. 2 829 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Model assessment: Prediction is "Oral LD50 = 2829,95 mg/kg", but the result may be not reliable as only moderately similar compounds with known experimental value in the training set have been found. Details are provided in attachment on the section: "attached full study report".

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The obtained results are disregarded as the substance is out from the applicability domain of the model.