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EC number: 231-955-3 | CAS number: 7782-42-5
- 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:
- 2010-02-24 to 2010-07-19
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Well performed GLP study according to recent OECD guideline
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:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Version / remarks:
- 2002
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Version / remarks:
- 2008
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Certificate attached to full study report
Test material
- Reference substance name:
- Graphite
- EC Number:
- 231-955-3
- EC Name:
- Graphite
- Cas Number:
- 7782-42-5
- Molecular formula:
- C
- IUPAC Name:
- carbon
- Test material form:
- solid: particulate/powder
1
Test animals
- Species:
- rabbit
- Strain:
- other: Russian Crl:CHBB
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Deutschland GmbH
- Age at study initiation: approx. 15 - 21 months
- Weight at study initiation: 2.8 - 3.1kg
- Housing: Individually in PPO cages (floor area: 2576cm^2)
- Diet (e.g. ad libitum): Altromin 2123, ad libitum
- Water (e.g. ad libitum): ad libitum, acidified with hydrochloric acid to pH 2.5 in order to prevent microbial growth
- Acclimation period: 7d
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C +/- 3°C
- Humidity (%): 30% - 70%
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12hrs/12hrs
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- other: clipped as closely as possible with an electrical clipper
- Vehicle:
- unchanged (no vehicle)
- Remarks:
- moistened with water
- Controls:
- no
- Amount / concentration applied:
- 0.5g
- Duration of treatment / exposure:
- 3min, 1hr, 4hrs
- Observation period:
- 24hrs, 48hrs, 72hrs
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- Area of exposure: 2.5cm x 2.5cm
- Type of wrap if used: 16-layer gauze patch; the patch was placed on the appropriate anterior test field moistened with water and secured semi-occlusively with adhesive Gothaplast tape (2.5cm)
REMOVAL OF TEST SUBSTANCE
- Washing (if done): mild soap and lukewarm water
- Time after start of exposure: 3min, 1hr and 4hrs
SCORING SYSTEM:
- According to OECD 404 and Regulation (EC) 440/2008 B.4, table 1 (see also section "Any other information on materials and methods incl. tables"
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animal 1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animal 1
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animal 2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animal 2
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animal 3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animal 3
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Reversibility:
- fully reversible
- Remarks on result:
- other: See section "Any other information on results incl. tables"
- Irritant / corrosive response data:
- The animal No. 4240 used in the initial test showed no skin reactions on the left and right test fields immediately after the termination of exposure. Also 1 hr after the termination of exposure a formation of erythema or oedema was not observed in animal No. 4240. Animal No. 4302 and No. 4331 from the confirmatory test showed no signs of skin irritation, too. On the subsequent days, 24 hrs, 48 hrs and 72 hrs after the termination of exposure, the animals No. 4240, No. 4302 and No. 4331 were free of skin reactions. The mean individual erythema scores after 4-hour exposure were 0.00, 0.00, 0.00, respectively. The mean individual oedema scores after 4-hour exposure were 0.00, 0.00, 0.00, respectively.
Any other information on results incl. tables
TABLE: Assessment of the formation of erythema and oedema within the first 72hrs after the termination of the exposure including the mean values calculated from the results of observation
Animal No. |
Weight in kg |
Exposure time |
Test field |
Observation assessment of the formation of erythema after the termination of exposure [hrs] |
Mean |
Observation assessment of the formation of oedema after the termination of exposure [hrs] |
Mean |
||||||||
0 |
1 |
24 |
48 |
72 |
0 |
1 |
24 |
48 |
72 |
||||||
4240 |
2.9 |
3 min |
al |
0 |
0 |
0 |
0 |
0 |
|
0 |
0 |
0 |
0 |
0 |
|
1 hr |
ml |
0 |
0 |
0 |
0 |
0 |
|
0 |
0 |
0 |
0 |
0 |
|
||
4 hrs |
pr |
0 |
0 |
0 |
0 |
0 |
0.00 |
0 |
0 |
0 |
0 |
0 |
0.00 |
||
4302 |
2.8 |
4 hrs |
al |
|
0 |
0 |
0 |
0 |
0.00 |
|
0 |
0 |
0 |
0 |
0.00 |
4331 |
3.1 |
4 hrs |
al |
|
0 |
0 |
0 |
0 |
0.00 |
|
0 |
0 |
0 |
0 |
0.00 |
Only the scores for the 4hr exposure
from the readings after 24hrs, 48hrs and 72hrs are included in the
calculation of the individual mean values
al = anterior left
ml = middle left
pr = posterior right
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on the results of the study described in this report, EXPANDED GRAPHITE POWDER has to be classified neither as irritant nor as corrosive according to the provisions laid down in regulation (EC) No 1272/2008 (2008).
- Executive summary:
The skin irritant effect of EXPANDED GRAPHITE POWDER was investigated according to the method recommended in the OECD Guideline 404 and the council regulation (EC) No. 440/2008 part B.4. Based on the critical analysis of all known data performed by the sponsor or monitor in his own responsibility the in vivo testing of the test item was considered to be justified. During an initial test using one female albino rabbit a sequential application (exposure time 3 min, 1 hr and 4 hrs) of EXPANDED GRAPHITE POWDER was carried out on one site of the left and right back area each. The skin was examined for signs of irritation straight after as well as 1 hr, 24 hrs, 48 hrs and 72 hrs after the termination of exposure. Since the animal did not show any signs of skin irritation within the observation period of 72 hours it was decided to carry out a confirmatory test with two additional animals in order to allow a categorization of the test item based on the classification criteria. Two female albino rabbits were exposed to the test item on one skin site of the back during the confirmatory test. After 4-hour exposure time the test item was removed and the skin was examined 1 hr, 24 hrs, 48 hrs and 72 hrs after the termination of exposure. These animals did not show any skin reactions, either. Under the experimental conditions described in this report the mean scores after the 4-hour exposure were:
Animal No. Erythema Oedema
4240 0.00 0.00
4302 0.00 0.00
4331 0.00 0.00
Based on the results of the study described in this report, EXPANDED GRAPHITE POWDER has to be classified neither as irritant nor as corrosive according to the provisions laid down in regulation (EC) No 1272/2008.
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