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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute oral toxicity: LD50>5000 mg/kg bw (standard acute method, limit test)
Acute dermal toxicity: LD50>10000 mg/kg bw (standard acute method, limit test)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
5 000 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
10 000 mg/kg bw

Additional information

Acute oral toxicity was tested in a standard acute limit test, in which a single dose of lemon oil (5000 mg/kg bw) was administered by oral gavage to 10 male Sprague-Dawley rats. No mortality was observed up to 14 days after application, therefore the oral LD50 was established to be >5000 mg/kg bw.

Acute dermal toxicity was also tested in a standard acute limit test, in which 6 female New Zealand White rabbits were exposed to a single dose of lemon oil (10000 mg/kg bw) dermally on the abraded abdominal skin. Based on the absence of mortality, a dermal LD50 >10000 mg/kg bw was established.

Justification for classification or non-classification

Based on the available information, lemon oil has been shown to be of low acute toxicity when applied via the oral and dermal route. Therefore, the substance lemon oil does not need to be classified for acute toxicity according to the criteria outlined in Annex I of 1272/2008/EC (CLP/EU-GHS) and Annex VI of 67/548/EEC.