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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 read across studies of C-6 normal and iso paraffins (hexanes) and naphthenes (methyl-cyclohexane, dimethylcyclohexane), 25-35% n-hexane (Hine et al., 1970; Klimisch score=2) were identified to support each acute toxicity endpoint (oral, dermal, and inhalation) for this substance.
Acute Toxicity-Oral LD50>16750 mg/kg in rats (OECD TG 401)
Acute Toxicity-Dermal LD50>3350 mg/kg in rabbits (OECD TG 402)
Acute Toxicity-Inhalation LC50>259354 mg/m3 in rats (OECD TG 403)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
16 750 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Dose descriptor:
LC50
Value:
259 354 mg/m³ air

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
3 350 mg/kg bw

Additional information

In a key read-across acute oral toxicity study of C-6 normal and iso paraffins (hexanes) and naphthenes (methyl-cyclohexane, dimethylcyclohexane), 25-35% n-hexane (Hine et al., 1970; Klimisch score=2), 6 male rats were administered doses up to 25 ml/kg of commercial n-hexane by oral gavage, and observed for 14 days post-dosing. No mortality was observed at any of the doses. The oral LD50 is therefore > 25 ml/kg (16750 mg/kg; density of 0.67) which makes the test substance not classified under EU criteria.

In a key read-across acute inhalation toxicity study (Hine et al., 1970; Klimisch score=2), groups of 10 male rats were exposed to concentrations of

C-6 normal and iso paraffins (hexanes) and naphthenes (methyl-cyclohexane, dimethylcyclohexane), 25-35% n-hexane

for 4 hours. Animals were then observed for clinical signs and mortality for at least 6 days post-exposure. Several animals died during the exposure period. Surviving animals experienced severe toxicological effects during the exposure. One animal experienced convulsions during and after exposure and died on day 6 post-exposure. The LC50 was determined to be 73,680 ppm (259354 mg/m3), and the test substance is therefore not classified under EU criteria.

In a key read-across acute dermal toxicity study of C-6 normal and iso paraffins (hexanes) and naphthenes (methyl-cyclohexane, dimethylcyclohexane), 25-35% n-hexa

ne (Hine et al., 1970; Klimisch score=2), 5.0 ml/kg was placed on the shaved skin of 3 male rabbits. The test area was then covered with a saran wrap sleeve for 4 hrs. After the exposure period, the test substance washed off, and the animals observed for toxicity and mortality over the next 14 days. No animals died; however, they did show signs of discomfort and uncoordination after the exposure. The LD50 for dermal exposure is > 5.0 ml/kg (3350 mg/kg). Therefore, the test substance is not classified under EU criteria.

Justification for classification or non-classification

The substance is not classified as acutely toxic under EU criteria. It is classified as a Category 1 aspiration hazard.