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EC number: 809-896-5 | CAS number: 60435-70-3
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Description of key information
No measured data are available for 2-methyl-1-heptanol so the data have been read-across from a structural analogue, the linear isomer octan-1-ol.
The acute oral key study in rat reports an LD50 of >5000 mg/kg for 1-octanol when applied as an aqueous solution (Henkel 1981; rel 2). The LD50 value of >5600 mg/m3 is reported in the key inhalation study in response to a 4 hour exposure to vapour (Amoco 1988; rel 2). The key study for acute dermal toxicity in rabbit found the LD50 value to be 2000-4000 mg/kg (Scientific Associates 1976; rel 2).
Key value for chemical safety assessment
Additional information
The acute key study reports no remarkable gross pathology at necropsy (Henkel 1981). The reliability 2 oral supporting study by Scientific Associates (1965) found the LD50 to be 18240 mg/kg in rat. The remaining supporting studies are reliability 4, and in accordance with the key information. The acute inhalation key study by Amoco (1988) was the only available information, with 5.6 mg/l as the highest dose tested. The clinical signs in response to the 4 hour inhalation exposure included signs of respiratory distress and histopathological evidence of irritation of the respiratory tract. However, the category trend suggests that the linear alcohols have low acute toxicity via the inhalation route. The acute dermal key study reported the most common gross pathological finding to be the erosion of the gastric mucosa (Scientific Associates 1976). The key studies were chosen based on the highest reliability and most recent available study report, and read-across to 2-methyl-1-heptanol.
Justification for classification or non-classification
Based on the available information for the read across substance, 1-octanol, the registration substance 2-methyl-1-heptanol does not require classification for any of the acute toxicity endpoints in accordance with CLP (EC regulation 1272/2008).
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