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EC number: 273-769-5 | CAS number: 69012-72-2 Residue from treatment of calcined zinc ore concentrates with antimony trioxide, zinc dust, lead oxide and copper sulfate. Consists primarily of zinc and a composite of metallics: cobalt, copper and lead.
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- December 1998 to December 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP Guideline study.
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 999
- Report date:
- 1999
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Principles of method if other than guideline:
- According to OECD Guideline 404 (Acute Dermal Irritation / Corrosion).
- GLP compliance:
- yes
Test material
- Reference substance name:
- Nickel sulphate
- EC Number:
- 232-104-9
- EC Name:
- Nickel sulphate
- Cas Number:
- 7786-81-4
- IUPAC Name:
- nickel(2+) sulfate
- Reference substance name:
- NiPERA.
- IUPAC Name:
- NiPERA.
- Details on test material:
- - Name of test material (as cited in study report): Nickel Sulfate Hexahydrate (10101-97-0)
- Molecular formula (if other than submission substance): not different than submission substance
- Molecular weight (if other than submission substance): not different than submission substance
- Smiles notation (if other than submission substance): not different than submission substance
- InChl (if other than submission substance): not different than submission substance
- Structural formula attached as image file (if other than submission substance): not different than submission substance
- Substance type: Pure product
- Physical state: blue-green crystalline powder
- Analytical purity: not reported
- Lot/batch No.: 08516TQ
- Stability under test conditions: not reported
- Storage condition of test material: stored at room temperature
- Other details not reported or not applicable
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Myrtle's Rabbitry, Thompson Station, TN, USA
- Age at study initiation: adult
- Weight at study initiation: not reported
- Housing: individually housed
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: minimum of 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19-21 deg. C
- Humidity (%): 20-50%)
- Air changes (per hr): not reported
- Photoperiod (hrs dark / hrs light): 12-hr light/dark cycle
IN-LIFE DATES: not reported
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- water
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g
VEHICLE
- Amount(s) applied (volume or weight with unit): 4 drops of deionized water - Duration of treatment / exposure:
- 4 hour(s)
- Observation period:
- up to 72 hours
- Number of animals:
- 3
- Details on study design:
- TEST SITE:
Approximately 24 hours pre-exposure, a patch of fur on the dorsal trunk area of three test animals was removed by close-clipping.
One animal had 3 separate skin sites prepared. The test substance (0.5 g moistened with deionized water) was applied to the exposed
skin via a semi-occlusive gauze patch. The patches were kept in contact with the skin for periods of 3 minutes, 1 hour, and 4 hours
(respectively, for the animal with 3 exposure sites), and 4 hours (for the remaining animals with only a single exposure site).
REMOVAL OF TEST SUBSTANCE:
- Washing (if done): After the respective exposure periods, the patches were removed and residual test material was removed using water.
- Time after start of exposure: 4 hours
SCORING SYSTEM:
The exposed skin sites were observed and evaluated for up to 72 hours following application. Animals were observed twice daily, and unusual observations and/or mortality were recorded. Animals were examined for signs of erythema and edema, and reactions were scored according to the Macroscopic Dermal Grading System based on Draize (1959). The 4-hour exposure data were classified according to EEC guidelines (1983) and mean scores were calculated to obtain Primary Irritation Indexes (PIIs) for erythema and edema.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 4-hour exposure
- Score:
- 0.42
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 4-hour exposure
- Score:
- 0
- Reversibility:
- fully reversible
- Irritant / corrosive response data:
- Exposure to the test substance for 3 minutes produced no dermal irritation.
Exposure to the test substance for 1 hour produced very slight erythema, which resolved completely by 48 hours.
Exposure to the test substance for 4 hours produced very slight erythema on 3/3 test animals one hour following patch removal.
The dermal irritation observed resolved completely in all test animals by the 48-h scoring interval.
Under the conditions of the test, there was no evidence that nickel sulfate hexahydrate was corrosive to the exposed skin of male and female
adult New Zealand White rabbits during exposure periods of 3 minutes, 1 hour, or 4 hours. - Other effects:
- none reported
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information
- Conclusions:
- Classification: not irritating
- Executive summary:
STUDY RATED BY AN INDEPENDENT REVIEWER.
ROBUST SUMMARY DEVELOPED BY AN INDEPENDENT REVIEWER.
Robust Summary for SLI (1999):
The potential irritant/corrosive effects of the test substance were evaluated using male and female adult New Zealand White rabbits, obtained
from Myrtle's Rabbitry, Thompson Station, TN, USA. Test animals were individually housed under constant conditions of temperature (19-21 deg.
C), relative humidity (20-50%), and photoperiod (12-hr light/dark cycle). Food and water were provided ad libitum.
Approximately 24 hours pre-exposure, a patch of fur on the dorsal trunk area of three test animals was removed by close-clipping. One animal had3 separate skin sites prepared. The test substance (0.5 g moistened with deionized water) was applied to the exposed skin via a semi-occlusive
gauze patch. The patches were kept in contact with the skin for periods of 3 minutes, 1 hour, and 4 hours (respectively, for the animal with 3
exposure sites), and 4 hours (for the remaining animals with only a single exposure site).
After the respective exposure periods, the patches were removed and residual test material was removed using water. The exposed skin siteswere observed and evaluated for up to 72 hours following application. Animals were observed twice daily, and unusual observations and/or
mortality were recorded. Animals were examined for signs of erythema and edema, and reactions were scored according to the Macroscopic Dermal
Grading System based on Draize (1959). The 4-hour exposure data were classified according to EEC guidelines (1983) and mean scores were
calculated to obtain Primary Irritation Indexes (PIIs) for erythema and edema.
Exposure to the test substance for 3 minutes produced no dermal irritation.
Exposure to the test substance for 1 hour produced very slight erythema, which resolved completely by 48 hours.
Exposure to the test substance for 4 hours produced very slight erythema on 3/3 test animals one hour following patch removal. The dermalirritation observed resolved completely in all test animals by the 48-h scoring interval.
Mean erythema score = 0.42 (nonirritant)
Mean edema score = 0.00 (nonirritant)
Under the conditions of the test, there was no evidence that nickel sulfate hexahydrate was corrosive to the exposed skin of male and femaleadult New Zealand White rabbits during exposure periods of 3 minutes, 1 hour, or 4 hours.
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