Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data migrated from NONS with permission to refer granted by ECHA.

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed
Year:
2013

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other: 92/69/EEC
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
liquid
Details on test material:
No information on test material available. Endpoint study information provided by ECHA from migrated NONS data and specific information not included.

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
unchanged (no vehicle)

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
794 mg/kg bw
Based on:
not specified
95% CL:
>= 483 - <= 1 305
Mortality:
2000 mg/kg bw: 5/5
1000 mg/kg bw: 2/5
Gross pathology:
No treatment-related macroscopic effects observed

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Remarks:
in accodance with CLP regulation (1272/2008/EC, as amended))
Conclusions:
Based on data provided by ECHA, the acute oral LD50 value is 794 mg/kg bw.