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Diss Factsheets
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EC number: 215-200-5 | CAS number: 1312-81-8
- 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
Lanthanum oxide was of low acute toxicity to rats via the oral and inhalation routes of exposure. No mortality and signs of toxicity were observed at the limit doses of 5000 and 10000 mg/kg bw via the oral route and 5.3 mg/L via the inhalation route of exposure. The analoguous substance lanthanum chloride was also tested via the dermal exposure route in rabbits and did not reveal any signs of toxicity at the limit dose of 2000 mg/kg bw.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Dose descriptor:
- discriminating dose
- Value:
- 10 000 mg/kg bw
Acute toxicity: via inhalation route
Endpoint conclusion
- Dose descriptor:
- discriminating conc.
- Value:
- 5 300 mg/m³ air
Acute toxicity: via dermal route
Endpoint conclusion
- Dose descriptor:
- discriminating dose
- Value:
- 2 000 mg/kg bw
Additional information
No mortality and signs of toxicity were reported in several literature references investigating the acute oral toxicity of lanthanum oxide up to dose levels of 10000 mg/kg bw in rats. A recent inhalation study with lanthanum oxide (4 h exposure to dust aerosols of a MMAF of 3.5 micro-m) according to modern guidelines and GLP did not reveal any mortality or test substance related signs of toxicity at a limit concentration of 5.3 mg/L. Similar results were obtained for the closeley related substance lanthanum carbonate. No acute dermal toxicity study is available for lanthanum oxide itsself, but an acute dermal toxicity study in rabbits with lanthanum chloride did not reveal any adverse effects at the limit dose of 2000 mg/kg bw of the test substance. As the dermal absorption of lanthanum oxide is considered very limited and lower than that of lanthanum chloride, no acute dermal toxicity is to be expected from dermal lanthanum oxide exposure. This conclusion is also supported by the low toxicity via the oral and inhalation routes of exposure.
Justification for classification or non-classification
Due to the low acute oral toxicity in rats: LD50, oral, rat > 10000 mg/kg bw, the low inhalation toxicity LC50, inhalation (4 h), rat > 5.3 mg/L and the low dermal toxicity of the structurally related lanthanum chloride LD50, dermal, rabbit > 2000 mg/kg bw, no classification for acute toxicity is warranted.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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