Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

The obtained results are disregarded as the substance is out from the applicability domain of the model.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
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
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
Control animals:
no
Sex:
not specified
Dose descriptor:
LD50
Effect level:
ca. 2 829 mg/kg bw
Based on:
test mat.

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".

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.
Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for selection of acute toxicity – oral endpoint
The obtained results are disregarded as the substance is out from the applicability domain of the model.

Justification for classification or non-classification

The obtained results are disregarded as the substance is out from the applicability domain of the model. Therefore, the substance is data lacking for this endpoint.