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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
other: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with national standard methods with acceptable restrictions
Remarks:
The test is conducted by means of Read Across approach. Further information was attached at section 13

Data source

Reference
Reference Type:
other: other company data
Title:
Unnamed
Year:
2018

Materials and methods

Principles of method if other than guideline:
Test method under evaluation
GLP compliance:
yes (incl. QA statement)
Test type:
other: test in progress

Test material

Constituent 1
Reference substance name:
Similar Substance 02 - AO061:1
IUPAC Name:
Similar Substance 02 - AO061:1
Test material form:
solid: particulate/powder

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levels
Remarks on result:
other: test in progress

Applicant's summary and conclusion

Conclusions:
Test in progress.