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EC number: 233-254-8 | CAS number: 10101-58-3
- 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 / corrosion
- Remarks:
- in vitro
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- July - September 2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Fully Guideline- and GLP-compliant
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.40 (In Vitro Skin Corrosion: Transcutaneous Electrical Resistance Test (TER))
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: OECD-Guideline 431, "In Vitro Skin Corrosion: Human Skin Model Test ", 13 April 2004
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: the OECD Guideline 439 “In Vitro Skin Irritation: Reconstructed Human Epidermis (RhE) Test Method”, 22 July 2010
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: ESAC statement, 5 November 2008
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: the Regulation (EC) 761/2009: B.46 "In vitro skin irritation: Reconstructed Human Epidermis Model Test". 23 July 2009
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- Cobalt wolframate
- EC Number:
- 233-254-8
- EC Name:
- Cobalt wolframate
- Cas Number:
- 10101-58-3
- Molecular formula:
- CoO4W
- IUPAC Name:
- cobalt wolframate
- Details on test material:
- Name of test material (as cited in study report): "COBALT WOLFRAMATE".
Trade name: Cobalt wolframate.
Chemical name: Cobalt wolframate.
Molecular formula: CoWO4.
Batch No.: 750702_20100329.
CAS No.: 10101-58-3.
Appearance: Dark blue powder.
Purity: Purity: > 98 %
Impurity: WO3 < 2 %.
Solubility: Not soluble in water.
Conditions of storage: At room temperature.
Stability at conditions of storage: Stable at room temperature.
Date of expiry: 31 May 2015.
Constituent 1
Test animals
- Species:
- other: in vitro system
- Strain:
- other: MatTek´s EpiDerm System
- Details on test animals or test system and environmental conditions:
- MatTek´s EpiDerm System consists of normal, human-derived epidermal keratinocytes which have been cultured to form a multilayered, highly differentiated model of the human epidermis. It consists of organized basal, spinous and granular layers, and a multi-layered stratum corneum containing intercellular lamellar lipid layers arranged in patterns analogous to those found in vivo. The EpiDerm™ tissues (surface 0.6 cm²) are cultured on specially prepared cell culture inserts (MILLICELLs, 10 mm ) and shipped as kits, containing 24 tissues on shipping agarose.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: n.a.
- Amount / concentration applied:
- The application spoon was filled with 25 mg finely grounded test substance. The "spoonful"
was levelled by gently scratching the excess material away, avoiding compression.
25 µL H2O were added for wetting of the test substance. - Duration of treatment / exposure:
- Epiderm Skin Corrosivity Test:
• 3 minutes
• 1 hour
Epiderm Skin Irritation Test:
• 60 minutes, post-incubation: 42 hours - Observation period:
- n.a.
- Number of animals:
- Epiderm Skin Corrosivity Test
Two tissue replicates were used for each treatment (exposure time), including distilled water
as negative and 8N KOH as positive control.
Epiderm Skin Irritation Test
Three tissue replicates were used, including distilled water as negative and 5 % SDS as
positive control. - Details on study design:
- Epiderm Skin Corrosion Test
Two tissue replicates were used for each treatment (exposure time), including deionised water as negative and 8N KOH as positive control.
Exposure times:
• 3 minutes
• 1 hour
50 μL of each reference substance were dispensed directly atop the EpiDerm™ tissue.
The application spoon was filled with 25 mg finely grounded test substance.
The "spoonful" was levelled by gently scratching the excess material away, avoiding compression.
25 µL H2O were added for wetting of the test substance.
Epiderm Skin Irritation Test
Three tissue replicates were used, including distilled water as negative and 5 % SDS as
positive control.
Exposure time:
• 60 minutes, post-incubation: 42 hours
30 μL of each reference substance were dispensed directly atop the EpiDerm™ tissue.
The application spoon was filled with 25 mg finely grounded test substance.
The "spoonful" was levelled by gently scratching the excess material away, avoiding compression.
25 µL H2O were added for wetting of the test substance.
MTT-test
After incubation with the test substance and washing with PBS, the tissues were incubated
with MTT medium at 37°C and 5 % CO2. After 3 hours, the MTT medium was aspirated from
all wells and the tissues were gently rinsed with PBS (2 times). For extraction, the tissues
were incubated with extractant solution (isopropanol) for 2 hours with shaking.
After the extraction period, the tissues were pierced with an injection needle and the extract
(now a blue formazan solution) was allowed to run into the well from which the tissue was
taken. The 24-well plates were placed on a shaker for 15 minutes until the solutions were
homogeneous in colour.
For the Epiderm Skin Corrosivity Test per each tissue 3 × 200 μL aliquots, for the Epiderm Skin Irritation Test
2 × 200 μL aliquots of the blue formazan solution were
transferred into a 96-well flat bottom microtiter plate and the OD was measured using
the extractant solution as blank in a plate spectrophotometer at 570 nm, without reference
filter.
Calculations
Cell viability
Cell viability was calculated for each tissue as percent of the mean of the negative control
tissues. The skin corrosivity/irritation potential of the test substance was classified according
to remaining cell viability obtained after test substance treatment with either of the two
exposure times.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- other: Mean tissue viability (%)
- Basis:
- mean
- Time point:
- other: 3 minutes
- Score:
- 104
- Reversibility:
- other: n.a.
- Remarks on result:
- other: Non-Corrosive
- Irritation parameter:
- other: Mean tissue viability (%)
- Basis:
- mean
- Time point:
- other: 1 hour
- Score:
- 103.2
- Reversibility:
- other: n.a.
- Remarks on result:
- other: Non-Corrosive
- Irritation parameter:
- other: Mean tissue viability (%)
- Basis:
- mean
- Time point:
- other: 60 minutes, 42 hours post-incubation
- Score:
- 97.3
- Reversibility:
- other: n.a.
- Remarks on result:
- other: Non-Irritant
- Irritant / corrosive response data:
- Epiderm Skin Corrosivity Test:
• The mean percentage viability of the treated skin discs after 3 minutes of exposure was
104.0 % which is above the threshold of 50 % for classification.
• The mean percentage viability of the treated skin discs after 1 hour of exposure was
103.2 % which is above the threshold of 15 % for classification.
Epiderm Skin Irritation Test:
• The mean percentage viability of the treated skin discs was 97.3 % which is above the
threshold of 50 % for classification. - Other effects:
- Epiderm Skin Corrosivity Test:
Assay acceptance criteria according to the protocol INVITTOX n°119 by ECVAM:
• The mean optical density (OD) of the tissues, treated with deionised water (negative
control) was 1.949 after 3 minutes, and 1.907 after 1 hour of exposure, that is higher than
0.8, as required by the assay acceptance criteria.
• The mean tissue viability of the 3 minutes positive control was 16.8 %, that is lower than
30 %, as required by the assay acceptance criteria.
• The maximum inter tissue viability differences of the "COBALT WOLFRAMATE" treated
skin discs were 2.6 % for 3 minutes and 2.5 % for 1 hour exposure, that is below 30 % as
required by the assay acceptance criteria
Epiderm Skin Irritation Test:
Assay acceptance criteria according to the protocol used during the ECVAM validation study:
• The mean OD of the tissues, treated with deionised water (negative control) was 2.030,
that is higher than 1.0 and lower than 2.5, as required by the assay acceptance criteria.
• The mean tissue viability of the positive control was 6.1 %, that is lower than 20 %,
as required by the assay acceptance criteria.
• The standard deviation calculated from individual percentual tissue viabilities of the
"COBALT WOLFRAMATE" treated skin discs was 2.0, that is below 18
as required by the assay acceptance criteria.
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- According to the results of this study, the Directive 2001/59/EC and the GHS, the test substance
"COBALT WOLFRAMATE" is considered to be non-corrosive and non-irritant to skin. - Executive summary:
Aim and Method
The EpiDerm Skin Corrosivity/Irritation Test (Model EPI-200) was performed to reveal possible irreversible tissue damages of the skin following the application of "COBALT WOLFRAMATE".
The test substance wastopically applied for 3 minutes and 1 hour to the epidermal surfaces ofthree-dimensional human epidermis models, followed by immediate determination of the cytotoxic effect. As there was no corrosive effect observed, the test substance wastopically applied for 60 minutes to the epidermal surfaces ofthree-dimensional human epidermis models. After a post-incubation of 42 hours, a cell viability test was performed.
· Investigations performed were in conformance with theRegulation (EC) 440/2008: B.40.BIS. "In vitro skin corrosion: human skin model", theOECD-Guideline 431, "In Vitro Skin Corrosion: Human Skin Model Test ", 13 April 2004, the OECD Guideline “In Vitro Skin Irritation: Reconstructed Human Epidermis (RhE) Test Method”, 22 July 2010, the ESAC statement, 5 November 2008 and theRegulation (EC) 761/2009: B.46 "In vitro skin irritation: Reconstructed Human Epidermis Model Test" 23 July 2009.
Results
EpiDerm Skin Corrosivity Test
Assay acceptance criteria according to the protocol INVITTOX n°119 by ECVAM:
· The mean optical density (OD) of the tissues, treated with deionised water (negative control) was 1.949 after 3 minutes, and 1.907 after 1 hour of exposure, that is higher than 0.8, as required by the assay acceptance criteria.
· The mean tissue viability of the 3 minutes positive control was 16.8 %, that is lower than 30 %, as required by the assay acceptance criteria.
· The maximum inter tissue viability differences of the"COBALT WOLFRAMATE"treated skin discs were 2.6 % for 3 minutes and 2.5 % for 1 hour exposure, that is below 30 % as required by the assay acceptance criteria.
"COBALT WOLFRAMATE":
· The mean percentage viability of the treated skin discs after 3 minutes of exposure was 104.0 % which is above the threshold of 50 % for classification.
· The mean percentage viability of the treated skin discs after 1 hour of exposure was 103.2 % which is above the threshold of 15 % for classification.
EpiDerm Skin Irritation Test
Assay acceptance criteria:
· The mean OD of the tissues, treated with deionised water (negative control) was 2.030, that is higher than 1.0 and lower than 2.5, as required by the assay acceptance criteria.
· The mean tissue viability of the positive control was 6.1 %, that is lower than 20 %, as required by the assay acceptance criteria.
· The standard deviation calculated from individual percentual tissue viabilities of the"COBALT WOLFRAMATE"treated skin discs was 2.0, that is below 18 as required by the assay acceptance criteria.
"COBALT WOLFRAMATE":
· The mean percentage viability of the treated skin discs was 97.3 % which is above the threshold of 50 % for classification.
Conclusion
According to the results of this study, the Directive 2001/59/EC and the GHS, the test substance
"COBALT WOLFRAMATE" is considered to be non-corrosive and non-irritant to skin.
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