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EC number: 282-500-0 | CAS number: 84238-45-9
- 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 skin sensitisation study with Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic is available, thus the skin sensitisation potential will be addressed with existing data on the individual assessment entities cerium andbenzenesulfonic acid, 4-C10-13-sec-alkyl derivs.Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic is not expected to show signs of dermal sensitisation, since the two moieties cerium andbenzenesulfonic acid, 4-C10-13-sec-alkyl derivshave not shown any skin sensitisation potential in animal studies.
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Cerium
The skin sensitisation potential of cerium chloride was evaluated by performing an in vivo local lymph node assay. In a range finding study 50% of cerium chloride was selected as maximum concentration suitable for dosing in solubility trials. The main study was performed with 10, 25 and 50% with 4 animals per dose. These concentrations were selected as at 50% no excessive irritation was noted. DPM served as positive control. At concentrations of 50% and 25%, the stimulation indexes are only slightly higher than the threefold increase in 3HTdR incorporation compared to the control values (4.29 and 4.44 respectively). It was observed that the test item has the potential to cause irritation as shown in the main test animals (50% and 25%). On this basis the test item can not be clearly classified as a sensitiser.
Thus, for clarification, a guinea pig maximisation test was performed. Intra-dermal injection of 0.01, 0.1, 0.5, 1, 2.5 and 5% cerium chloride as well as dermal application of 25, 50, 75 and 100 % were tested in a range finding study. Based on these results 0.01% cerium chloride were used for the induction exposure. Two weeks after the topical induction application, the animals were exposed to a dermal challenge dose of 100% or 50% (day 22 of treatment) for 24 hours. The control animals were treated similarly as the test group. Body weight, mortality and clinical signs were recorded. Under the conditions of the present assay the test item Cerium chloride was shown to have no sensitisation potential and classified as a non-sensitizer, according to current EU-regulations.
benzenesulfonic acid, 4-C10-13-sec-alkyl derivs
In a guinea pig maximization assay (Rose, 1983), A group of 10 male and 10 female guinea pigs were used to determine the potential of Benzenesulfonic acid, 4-C10-13-sec-alkyl derivs. to be sensitising to skin. The animals were first given an intradermal induction of 0.05% of test substance in corn oil. One week later, they were given a dermal induction of 5% test substance in corn oil. A group of 5 male and 5 female guinea pigs were used as controls. These animals were treated in a similar fashion with vehicle only. Two weeks after the dermal induction, a challenge was performed via dermal exposure to 2.5% test substance in corn oil. The control group was exposed as well. The animals were exposed for 24 hrs. Skin irritation readings were made at 24 and 48 hrs after the end of exposure. No positive responses were seen in either the test or control group. In summary, there is no evidence of sensitisation potential Benzenesulfonic acid, 4-C10-13-sec-alkyl derivs.
Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic
Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic is not expected to show signs of dermal sensitisation, since the two moieties cerium andbenzenesulfonic acid, 4-C10-13-sec-alkyl derivshave not shown any skin sensitising potential in animal studies. Further testing is not required. For further information on the toxicity of the individual assessment entities, please refer to the relevant section in the IUCLID.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic is not expected to show signs of dermal sensitisation, since the two assessment entities cerium andbenzenesulfonic acid, 4-C10-13-sec-alkyl derivshave not shown any skin sensitisation potential in experimental testing. Thus, Benzenesulfonic acid, 4-dodecyl-, cerium(4+) salt, basic is not to be classified according to regulation (EC) 1272/2008 as skin sensitising.
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