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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Expert Statement
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Justification for type of information:
Refer to Expert statement in attached background material

Data source

Reference
Reference Type:
other: Expert statement
Title:
Unnamed
Year:
2020

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
A Weight-of-Evidence based adaptation to the standard information requirement for acute oral toxicity study is provided in an expert statement.

Test material

Constituent 1
Chemical structure
Reference substance name:
3-(octyloxy)propane-1,2-diol
Cas Number:
10438-94-5
Molecular formula:
C11H24O3
IUPAC Name:
3-(octyloxy)propane-1,2-diol
Test material form:
liquid
Details on test material:
Storage Conditions: At room temperature protected from light container flushed with nitrogen.

Results and discussion

Effect levels
Remarks on result:
not measured/tested

Applicant's summary and conclusion

Interpretation of results:
other: Not classified
Remarks:
According to Regulation (EC) No. 1272/2008 and its amendments.
Conclusions:
Based on an expert statement, the substance is concluded to have a low toxicity (LD50 > 2000 mg/kg) and should not be classified for acute oral toxicity according to Regulation (EC) No 1272/2008 and related amendments.