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Diss Factsheets
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EC number: 701-480-0 | CAS number: -
- 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: well documented study performed according to internationally accepted method
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 001
- Report date:
- 2001
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.3 (Acute Toxicity (Dermal))
- Deviations:
- no
- GLP compliance:
- no
- Remarks:
- other quality assurance
- Test type:
- fixed dose procedure
- Limit test:
- yes
Test material
- Reference substance name:
- Iron silicate, copper smelting and refining
- EC Number:
- 701-480-0
- Cas Number:
- 67711-92-6
- IUPAC Name:
- Iron silicate, copper smelting and refining
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- The animals were kept to acclimate to laboratory conditions during the five days preceding the survey.
The rats were housed in a cage with individual identification. The diet was standard for these animals.
The temperature of the animal room was maintained at 22 + / - 3, the relative humidity in the range of 30-70% and also maintained a photoperiod of 12/12 light / dark.
Approximately 24 hours before the test, fur was be removed by shaving from the dorsal area.
Administration / exposure
- Vehicle:
- unchanged (no vehicle)
- Doses:
- Single dose 2000 mg/kg bw
- No. of animals per sex per dose:
- 1
- Control animals:
- yes
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- No
- Other findings:
- The animals survived and there were no changes in their behavior.
Any other information on results incl. tables
Table 1
Animal |
Sample |
Sex |
Weight initial (g) |
Weigh final (g) |
Observation |
3 |
control |
female |
150 |
189.5 |
No dermal reaction |
4 |
sample |
female |
165.5 |
192 |
No dermal reaction |
The animals survived and no changes observed in their behavior. |
Applicant's summary and conclusion
- Interpretation of results:
- practically nontoxic
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Good quality study. No negative effects were observed. An LD 50 of > 2000 mg/kg bw was assessed
- Executive summary:
The dermal toxicity of copper slag was assessed during an acute toxicity limit test with rat. The test was performed according to EU B3 Method (Limit-test). All test animals were exposed to 2000 mg copper slag/kg bodyweight. After 14 days of observation, none of the animals showed negative effects. An LD 50 of > 2000 mg/kg bw was assessed.
Therefore copper slag is considered as nontoxic via dermal route.
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