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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
other: expert assessment
Adequacy of study:
key study
Study period:
2020
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: An assessment was conducted based on the information on the individual constituents of the substance
Qualifier:
no guideline required
Principles of method if other than guideline:
An assessment was conducted based on the information on the individual constituents of the substance
GLP compliance:
no
Test type:
other: An assessment was conducted based on the information on the individual constituents of the substance
Limit test:
no
Remarks on result:
other: An assessment was conducted based on the information on the individual constituents of the substance
Interpretation of results:
GHS criteria not met
Conclusions:
No conclusion could be reached, therefore, an animal study must be conducted on fatty acids, C16-18, reaction products with ethanolamine.
Executive summary:

An assessment was conducted based on the information on the individual constituents of the substance. No conclusion could be reached, therefore, an animal study must be conducted on the substance.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

Justification for classification or non-classification