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EC number: 265-103-7 | CAS number: 64742-04-7 A complex combination of hydrocarbons obtained as the extract from a solvent extraction process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50. This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.
- Life Cycle description
- Uses advised against
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- Endpoint summary
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- Ecotoxicological Summary
- Aquatic toxicity
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- Short-term toxicity to fish
- Long-term toxicity to fish
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- Long-term toxicity to aquatic invertebrates
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- Endocrine disrupter testing in aquatic vertebrates – in vivo
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- Toxicological Summary
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- Irritation / corrosion
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Carcinogenicity
Administrative data
Description of key information
Distillate aromatic extract was found to have carcinogenic potential when applied repeatedly to the clipped skin of mice.
Key value for chemical safety assessment
Carcinogenicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Carcinogenicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Carcinogenicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LOAEL
- 100
- Study duration:
- chronic
- Species:
- mouse
Justification for classification or non-classification
Based on the incidence of cancer after dermal exposure, distillate aromatic extracts are classified as Carcinogenic, Category 1B (H350) according to the EU CLP Regulation (EC No. 1272/2008).
Additional information
Four well conducted skin painting studies in mice were identified. In the key study, 50 uL aliquots of material were applied twice / week for 2 years to the clipped skin of mice. Following treatment there was an increased incidence of skin tumours compared to controls, Thirty one of 42 mice showed tumours, with an average latency period of 52 weeks.
In further study (Gradiski, 1983) mice were treated with 0.05 millilitres of undiluted test material three times weekly for the first month and twice weekly for the next 11 months to the shorn dorsal lumbar skin of a group of 30 mice. A group of 60 female mice shaved once weekly served as untreated controls.
At study termination, depilation and cutaneous atrophy was noted and attributed to skin irritation or repeated scratching. Eight-three percent of animals treated with distillate aromatic extract developed one or more skin tumours; 33% benign, 17% malignant and 33% benign and malignant. Observed malignant tumours included squamous cell carcinomas and sarcomas. By comparison, no skin tumours or cutaneous lesions were observed in any of the white oil or untreated control animals.
The authors concluded that dermal exposure to the tested distillate aromatic extract, in addition to causing skin irritation, resulted in skin cancer in the mouse. It was observed that general mortality decreases as the refinement of the oil increases. Distillate aromatic extract, which contains polycyclic aromatic hydrocarbon substances, produced a significant biological response and was found to be carcinogenic.
Justification for selection of carcinogenicity via dermal route endpoint:
Well conducted 2 yr skin painting study. One of 4 studies showing similar results
Carcinogenicity: via dermal route (target organ): other: skin
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