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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

One key study (Hine et al., 1970; Klimisch score=2) was identified to support each acute toxicity endpoint (oral, dermal, and inhalation).
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

The acute toxicity of hexane solvent containing between 5 and 80% n-hexane has been fully evaluated.  All of the animal studies were performed in a manner similar or equivalent to currently established OECD guidelines.  Based on data for commercial hexane, this substance has a low order of acute toxicity by the oral, dermal, and inhalation routes of exposure.

In a key acute oral toxicity study (Hine et al., 1970; Klimisch score=2), 6 male rats were administered doses up to 25 ml/kg of commercial 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 this substance not classified under EU criteria.

In a key acute dermal toxicity study (Hine et al., 1970; Klimisch score=2), 5.0 ml/kg of test substance 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, this substance is not classified under EU criteria.

In a key acute inhalation toxicity study (Hine et al., 1970; Klimisch score=2), groups of 10 male rats were exposed to concentrations of commercial hexane vapor 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 this substance is therefore not classified under EU criteria.

Justification for classification or non-classification

The test substance, C6 aliphatics, 5-80% n-hexane, is classified as a Category 1 aspiration hazard.