Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: dermal
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
the study does not need to be conducted because the substance does not meet the criteria for classification as acute toxicity or STOT SE by the oral route and no systemic effects have been observed in in vivo studies with dermal exposure (e.g. skin irritation, skin sensitisation)
Cross-reference
Reason / purpose for cross-reference:
data waiving: supporting information
Reference
In a study performed with the test substance 2 -hexyldecanoic acid the oral LD50 was > 2020 mg/kg. 
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
Value:
2 020 mg/kg bw
Endpoint conclusion:
no study available
Endpoint conclusion:
no study available

2 Hexyldecanoic acid on the available acute toxicity information does not present an acute toxicity hazard and does not require classification according Regulation (EC) No 1272/2008.

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion