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EC number: 310-079-6 | CAS number: 102242-48-8 The complex residue resulting from the vacuum distillation of C6-24 and C6-24 unsatd. fatty alcohols which is derived from hydrogenation of C6-24 and C6-24 unsatd. fatty acids methyl esters. It consists predominantly of satd. and unsatd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
- 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
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
The test item was tested for sensitising potential according to the Buehler Testing Method, as described in the OECD TG 406 (Henkel R9300244). The treatment group comprised 20 and the control group 10 female Guinea pigs; an additional group of 5 animals was used for determination of the maximal non-irritating concentration suitable for challenge.
According to preliminary and dose finding tests, the concentration of test item for induction was set at 50% in oleum arachidis DAB 10 whereas it was 20% for the first challenge, and 10% for the rechallenge. After triple (once a week) epicutaneous application (occlusive/6 h), the first challenge (occlusive/6 h) was performed after 14 days and was followed by a rechallenge (occlusive/6 h) after 21 days following induction. Following first challenge, up to 80% of the animals of the treatment group and up to 70% of the animals of the control group showed weak to moderate skin reactions. Following rechallenge, up to 20% of the animals of the treatment group and up to 30% of the animals of the control group showed almost weak skin reactions. Since the incidence of skin reactions following challenge and rechallenge was within the same range for both, the control and the treatment group, the present test gives no indication of a sensitising potential for the test item.
Migrated from Short description of key information:
A Buehler Test conducted according to the OECD TG 406 is available (Henkel R 9300244, 1993); the test gave no indication of a sensitising potential for the test item.
Respiratory sensitisation
Endpoint conclusion
- Additional information:
- Migrated from Short description of key information:
No data available
Justification for classification or non-classification
According to the results of a Buehler test, "Alcohols, C6-C24 and C6-C24 unsat., distn residues"(CAS 102242-48-8) is not expected to be sensitising and thus, neither classification according to the EU Directive 67/548/EEC nor classification according to the EU CLP Regulation (EC) No. 1272/2008 is needed.
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