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EC number: 218-679-9 | CAS number: 2215-35-2
- 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
This substance is an EU Category 2 skin irritant and an EU Category 1 eye irritant with a specific concentration limit of 10% for eye irritation.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
In a key study this substance was applied to white rabbits under semi-occlusive dressing for four hours (Kern, TG, 1999). The test material was administered at concentrations of 100, 50, 25, and 12.5% in mineral oil. The primary irritation index of 4.84, 4.58, 3.93, and 3.08 were calculatedfor the 100, 50, 25, and 12.5% w/v concentrations, respectively. The mean 24 to 72 hour erythema scores were determined to be 3.0, 2.94, 2.84, and 2.33 for 100, 50, 25, and 12.5% w/v concentrations, respectively, and the mean 24 to 72 hour edema scores were determine to be 1.83, 1.67, 1.11, and 0.83 for 100, 50, 25, and 12.5% w/v concentrations, respectively.
In a key study, this substance was instilled into the conjunctival sac of white rabbits(Hershman, RJ and Moore, GE, 1983). The mean eye irritation scores were 22.3, 18.7, 18.3, 9.3, and 2.3 at days 1, 2, 3, 4, and 7, respectively. The mean (24, 48, and 72 hour) cornea opacity, iritis, conjunctival erythema and conjunctival edema scores were 0.49, 0.33, 1.36, and 1.94, respectively. The test substance was an irritant.
In a supporting study this substance was instilled into the conjunctival sac of white rabbits at concentrations of 10% in mineral oil (Hershman, RJ and Moore, GE, 1983). The mean eye irritation scores were 0.3 at day 1 and 0.0 on days 2 through 7. The mean (24, 48, and 72 hour) cornea opacity, iritis, conjunctival erythema and conjunctival edema scores were 0.0, 0.0, 0.0, and 0.06, respectively. The 10% solution of the test substance in mineral oil was not an irritant
Effects on skin irritation/corrosion: moderately irritating
Effects on eye irritation: highly irritating
Justification for classification or non-classification
This substance meets the requirement under EU CLP (Regulation (EC) No. 1272/2008) for classification as a Category 2 skin irritant and a Category 1 eye irritant with a specific concentration limit of 10% for eye irritation.
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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