Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: - | 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
Short-term toxicity to fish
Administrative data
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 02 Apr - 03 May 2009
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- Due to the nature of the test item, analytical measurement is not possible.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 009
- Report date:
- 2009
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- 1992
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Qualifier:
- according to guideline
- Guideline:
- other: OECD No.23 Guidance document on aquatic toxicity testing of difficult substances and mixtures
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- THE DEPARTMENT OF HEALTH OF THE GOVERNMENT OF THE UNITED KlNGDOM, UK GLP Monitoring Authority
Test material
- Reference substance name:
- Vapour grown graphitic carbon fibre
- Molecular formula:
- C
- IUPAC Name:
- Vapour grown graphitic carbon fibre
Constituent 1
Sampling and analysis
- Analytical monitoring:
- no
- Remarks:
- Due to the nature of the test item, analytical measurement is not possible.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Differential loading: Since a limittest was conducted the only test item concentration was 100 mg/L. The test solution was prepared by stirring the appropriate amount of test material in 20 L of test media for 48 h at 21 - 23 °C. At the end of the stirring phase the dispersion was settled for 4 h. The aqueous phase was seperated from the bulk of the undissolved material and filtered using a Whatman No.1 filter paper. The resultant solution was used as the test exposre solution.
- Controls: Medium without test item
Test organisms
- Test organisms (species):
- Cyprinus carpio
- Details on test organisms:
- TEST ORGANISM
- Common name: Common carp
- Source: Hampshire Carp Hatcheries; Bow Lake Fish Farm, Hampshire, UK
- Mean length at the end of the study: 56.2 mm
- Mean weight at the end of the study: 1.79 g
ACCLIMATION
- Acclimation period: 20 - 29 Apr 2009
- Acclimation conditions: Same as test conditions:Temperature: 21.5 - 23.5 °C; Dissolved oxygen: >81% ASV; Photoperiod: 16 h light and 8 h dark
- Type and amount of food during acclimation: The carp are fed with Hikari Staple carp food approximately 2% body weight per day until 24 h before test initiation.
- Feeding frequency during acclimation: daily
- Health during acclimation (any mortality observed): 3.3% mortality during acclimation period
FEEDING DURING TEST : The carp were not fed during the test
Study design
- Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
Test conditions
- Hardness:
- 183 mg CaCO3/L
- Test temperature:
- 21.0 - 22.5 °C (Control)
21.0 - 23.0 (100 mg/L) - pH:
- 7.7 - 8.1 (Control)
7.9 - 8.1 (100 mg/L) - Dissolved oxygen:
- 75 - 100% ASV (Control)
86 - 99% ASV (100 mg/L) - Nominal and measured concentrations:
- Control and 100 mg/L (nominal loading rate)
- Details on test conditions:
- TEST SYSTEM
Test vessel:
- Type: open
- Material, size, headspace, fill volume: 28 L volume aquaria, 20 L test volume, 8 L headspace
- Renewal rate of test solution (frequency/flow rate): every 24 h
- No. of organisms per vessel: 7
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Dechlorinated main water with reverse osmosis purified water added appropriately to lower the hardness. The ratio of dechlorinated mains water to reverse osmosis water was 75:25. The hardness was calculated after mineral analysis on a sample of dilution water.
- Culture medium different from test medium: same medium was used
- Intervals of water quality measurement: The pH (to 0.1), dissolved oxygen (to 1% ASV) and temperature (to 0.5 °C) were measured. Water quality determinations for each test and control solution were carried out immediately prior to initiating the test, before and after each daily change of the test solutions and at the end of the 96 h exposure period.
OTHER TEST CONDITIONS
- Photoperiod: 16 h light and 8 h dark
EFFECT PARAMETERS MEASURED: Observations and records of mortalities were made after 24, 48, 72 and 96 h exposure period.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: no spacing facter was used since only one test item concentration was tested
Range finding study
- Test concentrations: 0, 0.1, 1.0, 10 and 100 mg/L
- Results used to determine the conditions for the definitive study data from the preliminary study identified the 96 h LL50 as being greater than 100 mg/L. - Reference substance (positive control):
- yes
- Remarks:
- Copper (II) Sulphate (CuSO4・5H2O)
Results and discussion
Effect concentrations
- Duration:
- 96 h
- Dose descriptor:
- LL50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- - Behavioural abnormalities: No abnormal behaviour was observed.
- Mortality of control: No mortality was observed. - Results with reference substance (positive control):
- LC50 (96h): 4.6 mg/L (95% confidential limits: 2.9 - 7.2 mg/L)
- Reported statistics and error estimates:
- All LC50 and NOEC results are calculated using ToxCalc Version 5.0 "Comprehensive Toxicity Data Analysis and Database Software"
Any other information on results incl. tables
- Sublethal observations / clinical signs:
Biological Results:
The 96 h LL50 value of the test item to Carp was estimated to be greater than 100 mg/L. The highest no observed effect loading rate (NOELR) after 96 h was 100 mg/L.
Table 1: LL50 and NOELR values (based on the nominal loading rate)
Period of exposure (h)
LL50 value
95% confidence limits
NOELR
24
>100 mg/L
Not possible to determine
100 mg/L
48
>100 mg/L
Not possible to determine
100 mg/L
72
>100 mg/L
Not possible to determine
100 mg/L
96
>100 mg/L
Not possible to determine
100 mg/L
Table 2: Abnormal behavior
Period of exposure (h)
Nominal loading rate (mg/L)
Control
100
0
7 n
7 n
24
7 n
7 n
48
7 n
7 n
72
7 n
7 n
96
7 n
7 n
N: number of carp displaying normal behaviour
Table 3: Cumulative mortalities
Period of exposure (h)
Nominal loading rate (mg/L)
Control
100
0
0
0
24
0
0
48
0
0
72
0
0
96
0
0
Table 4: Validity criteria
Criterion from the guideline
Outcome
Validity criterion fulfilled
The mortality in the control(s) should not exceed 10% (or one fish if less than ten are used) at the end of the test
No mortality was observed
Yes
The dissolved oxygen concentration must have been at least 60 per cent of the air
saturation value throughout the test
Oxygen concentration ≥ 60%
Yes
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Remarks:
- For further details please refer to “Any other information on results incl. tables”.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.