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EC number: 271-239-8 | CAS number: 68526-91-0 A complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isotridecanal from the hydroformylation of dodecene. It consists predominantly of C13-14 primary aliphatic alcohols, C22-28 dimer alcohols, C26 acetals and esters, and C>10 acid sodium salts and boils in the range of approximately 250°C to 450°C (482°F to 842°F).
- 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
skin irritation
in vivo, rabbit, occlusive, 4h: not irritant (standardized method, OECD 404, BASF AG, 1982)
eye irritation
in vivo, rabbit: not irritant according to 67/548/EEC; Cat. 2 according to 1272/2008/EC CLP (standardized method, OECD 405, BASF AG, 1982)
respiratory irritation
no data available
Key value for chemical safety assessment
Additional information
There are reliable studies available to assess the potential of the substance for skin and eye irritation.
Skin irritation:
An OECD 404 guideline conform study was performed to assess the acute dermal irritation or corrosion potential of the test substance Oxooel 13 in Vienna White rabbits (BASF AG, 1982). Three rabbits were dermally exposed to 0.5 ml of the test substance for 4 hours under occlusive conditions. Irritation was scored by the method of Draize as described in the OECD guideline 404. The mean score for the 24, 48 and 72 h reading for erythema were 1.3, 1.7 and 2 in the three animals. Edema was not observed in any animal at any reading. The findings were fully reversible in all animals within 8 days after application, thus the study was terminated.
Under the conditions of this study, the test substance is not considered to be a dermal irritant.
Eye irritation:
To assess the acute eye irritation potential of the test substance Oxooel 13 in vivo an eye irritation test in Vienna White rabbits was performed according to the method described in OECD guideline 405 (BASF AG, 1982).
An amount of 0.1 ml of the test substance was single ocular applied to three rabbits and left unwashed after application. The average scores (24 to 72 hours) were calculated to be 0.0 for corneal opacity and iris, 1.9 for conjunctivae redness and 0.8 for chemosis. The findings were reversible in all animals at the latest within 8 days after application, thus the study was terminated. Redness of the conjunctiva with a score of 2 was observed in two of three animals, therefore GHS classification is required (category 2). Slightly discharge in two animals and clearly discharge in one male animal increased 24 hrs after application but were reversible within 48 hrs after application. In addition, constricted pupil 24 hours after application was observed in one female. These symptoms were reversible within 48 hours.
Under the test conditions chosen and considering the described findings the test substance does not give indication of an irritant property to the eye under 67/548/EEC. According to 1272/2008/EC CLP, Oxooel 13 has to be classified as irritating to eye (Category 2).
respiratory irritation
no data available
Effect level: empty Endpoint conclusion: Adverse effect observed
Justification for classification or non-classification
skin irritation:
Dangerous Substance Directive (67/548/EEC):
The available studies are considered reliable and suitable for classification purposes under 67/548/EEC. As a result the substance is not considered to be classified for skin irritation under Directive 67/548/EEC, as amended for the 28th time in Directive 2001/59/EC.
Classification, Labeling, and Packaging Regulation (EC) No. 1272/2008:
The available experimental test data are reliable and suitable for classification purposes under Regulation 1272/2008. As a result the substance is not considered to be classified for skin irritation under Regulation (EC) No. 1272/2008.
eye irritation:
Dangerous Substance Directive (67/548/EEC):
The available studies are considered reliable and suitable for classification purposes under 67/548/EEC. As a result the substance is not considered to be classified for eye irritation under Directive 67/548/EEC, as amended for the 28th time in Directive 2001/59/EC.
Classification, Labeling, and Packaging Regulation (EC) No. 1272/2008:
The available experimental test data are reliable and suitable for classification purposes under Regulation 1272/2008. As a result the substance is considered to be classified as irritating to eye (Cat. 2) under Regulation (EC) No. 1272/2008.
respiratory irritation
no data available
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