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Description of key information

The key study for acute oral toxicity reports an LD50 value of >5000 mg/kg in rat (Biolab 1990; rel 2). The acute dermal study reports an LD50 value of 6180mg/kg (Lifestream Laboratories, 1966; rel 2)

Key value for chemical safety assessment

Additional information

Information available for C14 -15 Alcohols-branched and linear can be freely ready-across to Alcohols, C14 -15 predominantly linear. The branched strcutures do no confer different toxicological properties to the predominantly linear aliphatic alcohols. So key studies have been chosen from studies on closely related linear or branched alcohols of similar chain length.

The most recent and high reliability information was assigned as key studies. The data for acute inhalation toxicity was waived on the premise that high reliability data were available via the oral and dermal routes, in accordance with current REACH requirements, Section 5.2 in Annex VIII. Furthermore, based on the information on other alcohols across category, the LC50 for inhalation toxicity is expected to be greater than the substantially saturated vapour concentration.

In addition to the exisiting key studies for acute oral and dermal toxicity, high reliability supporting studies are also available which are in accordance with the key findings.

In some cases the CAS and chemical identity stated refer to SDA nomenclature for this substance. In REACH substance identification it is necessary to be more specific as to the chain lengths present. Full details may be found in the CSR

Justification for classification or non-classification

Acute toxicity tests do not indicate any potential hazard for acute, dermal or inhalation toxicity. Tests on similar substances included in this category are also supportive of these results; which do not warrant classification for any acute toxicity endpoint under DSD or GHS criteria. The substance is therefore not classified for acute toxicity in accordance with EC regulation 1272/2008.