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EC number: 284-183-4 | CAS number: 84803-57-6
- 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
In an EpiDerm™ Corrosivity-Test and a HET-CAM in vitro corrosion test it is concluded that the test substance is not corrosive to either skin and eye. In vivo studies for skin and eye irritation with a structural analogue showed no potential for eye or skin irritation.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin irritation/corrosion
The corrosive potential was determined in an EpiDerm™ Corrosivity-Test in vitro. Two EpiDerm™ tissue samples were incubated with the test substance for 3 minutes and 1 hour, each (BASF 2003). Tissue viability was determined after exposure to the test substance. There was no decrease in tissue viability observed after 3 minute or 1 hour exposure. Based on these results the test substance was considered to be non-corrosive.
The potential of the structural analogue 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile to cause acute dermal irritation or corrosion was assessed in a OECD 404 guideline study (compiant with GLP), by a single topical application of an amount of 0.5 g of the test substance for 4 hours to the intact skin of three White New Zealand rabbits, using a patch of 2.5 cm x 2.5 cm covered with semiocclusive dressing (BASF 2008). After removal of the patch, the application area was washed off. The cutaneous reactions were assessed immediately after removal of the patch and approximately 1, 24, 48, and 72 hours after removal. Slight or moderate erythema was observed in all animals up to 1 hour after removal of the patch. The cutaneous reactions were reversible in all animals within 24 hours after removal. The average score (24 to 72 hours) for irritation was calculated to be 0 for erythema and for edema. It was concluded that the test substance was not irritating to the skin.
Eye irritation
The potential to cause serious eye damage was determined in a HET-CAM in-vitro corrosion test (alternative method to study the potential of serious damage to the eyes/mucous membranes in incubated hen eggs) (BASF 2003). Three hen eggs were exposed to the test substance for 180 seconds. The test substance produced no coagulation, lysis or heamorrhagia effects within a relevant time period after application.
In an OECD 405 guideline study performed in accordance with GLP, the potential of the the structural analogue 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile to cause damage to the conjunctiva, iris or cornea was assessed by a single ocular application of 0.1 mL bulk volume (about 37 mg) of the test substance to one eye of three White New Zealand rabbits (BASF 2008). About 24 hours after application the eye was rinsed with tap water. The ocular reactions were assessed approximately 1, 24, 48 and 72 hours after application. The average score (24 to 72 hours) for irritation was calculated to be 0 for corneal opacity, iris, chemosis, and 0.4 for conjunctival redness (in which three animals had a score of 0.7, 0.3 and 0.3 respectively). The findings were reversible within 72 hours after application. It was concluded that the test substance was not irritating to the eye.
Justification for selection of skin irritation / corrosion endpoint:
One skin corrosion in vitro study and one in vivo skin irritation study with an structural analogue are available. These studies are adequate for covering the endpoint.
Justification for selection of eye irritation endpoint:
One in vitro study on eye damage and one study on in vivo eye irritation of an structural analogue are available. These studies are adequate for covering the endpoint.
Justification for classification or non-classification
Based on the findings in the skin and eye corrosion study, the test substance is considered to be not corrosive. According to these results and negative in vivo skin and eye irritation studies with the structural analogue 4-tert-Butyl-3-hydroxy-2,6-xylylacetonitrile, classification according to the EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008 and the Directive 67/548/EEC (DSD) is not 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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