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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

LD50 oral (rat): > 5000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
> 5 000 mg/kg bw

Additional information

oral:

In an acute oral toxicity study performed according to the Acute Toxic Class Method, a dose of 5000 mg/kg bw of the undiluted test item 2-Propenoic acid, 2-methyl-, C13-15-branched and linear alkyl esters was administered by gavage to two test groups (limit test) of three fasted Wistar rats (starting with one animal and supplementing two additional animals). Neither mortality nor clinical signs were observed in the three administered animals. All animals gained weight in a normal range throughout the study period. There were no macroscopic pathological findings in any animal sacrificed at the end of the observation period (3 females). The acute oral LD50 was assessed to be LD50, oral, rat > 5000 mg/kg bw

Justification for classification or non-classification

Based on the results, the test item was not classified and labelled according to Regulation (EC) No 1272/2008 (CLP).