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Diss Factsheets
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A reaction mixture containing the following components;A. Tetralithium [2(or 3), 9 (or 10), 16 (or 17), 23 (or 24)-tetrakis (3-sulfonato-propylsulfonyl) phthalocyaninato]cupurate (II)B. Trilithium [3-(2-hydroxylpropylsulfamoyl)propylsulfonyl]tris (3-sulfonato-propylsulfonyl)phthalocyaninatocupurate (II)C.Dilithium bis [3-(2-hydroxylpropylsulfamoyl)propylsulfonyl] bis (3-sulfonato-propylsulfonyl)phthalocyaninatocupurate (II)D. Lithium tris [3-(2-hydroxylpropylsulfamoyl)propylsulfonyl] (3-sulfonato-propylsulfonyl)phthalocyaninatocupurate (II)E. Tetrakis [3-(2-hydroxpropylsulfamoyl) proppylsulfonyl]phthalocyaninatocupurate (II)In the ratio A:B:C:D:E 6.25 : 25 : 37.5 : 25 : 6.25
EC number: 472-040-0 | 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
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_ecotoxicological-information.png)
Short-term toxicity to aquatic invertebrates
Some information in this page has been claimed confidential.
Administrative data
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- The range-finding test was conducted between 7 January 2003 and 9 January 2003 and the definitive test between 3 February 2003 and 5 February 2003. The final report was issued 28th March 2003.
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Meets the criteria for classification as Reliable without restriction according to Klimisch et al (1997)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 003
- Report date:
- 2003
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: 92/69/EEC,method C2 of commission directive 92/69/EEC which constuitutes Annex V of council directive 67/548/EEC
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Test material form:
- solid
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
Test solutions
- Vehicle:
- no
- Details on test solutions:
- Identity and concentration of auxiliary solvent for dispersal: None used
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Adult Daphnia were maintained in polypropylene vessels containing approximately 2 litres of reconstituted water in a temperature controlled room at 21°C. The lighting cycle was controlled to give a 16 hours light and 8 hours darkness cycle with 20 minute dawn and dusk transition periods. Each culture was fed daily with a suspension of algae (Chlorella sp.). Culture conditions ensured that reproduction was by parthenogenesis. Gravid adults were isolated the day before initiation of the test, such that the young daphnids produced overnight were less than 24 hours old. These young were removed from the cultures and used for testing. The diet and diluents water are considered not to contain any contaminant that would affect the integrity or outcome of the study.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- 250 mg CaCO3/L
- Test temperature:
- 20.7 - 20.9 degrees C
- pH:
- 7.8 - 8.0
- Dissolved oxygen:
- 91 - 93 %ASV (air saturation value)
- Nominal and measured concentrations:
- The test substance concentration was measured spectrophotometrically using an external standard.
- Details on test conditions:
- TEST SYSTEM- Test vessel: 250ml glass jars- No. of organisms per vessel: 10- No. of vessels per concentration (replicates):2- No. of vessels per control (replicates):2OTHER TEST CONDITIONS- Photoperiod: 16hr light 8hr dark with 20 min dawn/dusk transitionEFFECT PARAMETERS MEASUREDAny immobilisation or adverse reactionsTEST CONCENTRATIONS- Range finding study: 0.010, 0.10, 1.0 and 10 mg/L- Test concentrations:1.8, 3.2, 5.6, 10, 18, 32, 56, 100, 180 mg/L
- Reference substance (positive control):
- no
Results and discussion
Effect concentrationsopen allclose all
- Key result
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 180 mg/L
- Conc. based on:
- test mat.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 180 mg/L
- Conc. based on:
- test mat.
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 10 mg/L
- Conc. based on:
- test mat.
- Details on results:
- In the range finding test, 30% immobilisation was observed at the 100 mg/L test concentration after 48h exposure. Based on this result a test concentration of 1.8 to 180 mg/L was assigned to the definitive test in an attempt to calculate a 48h EC50. However, only 35% immobilisation was observed by 48h at 180 mg/L in the definitive test so an EC50 could not be calculated. It was considered unnecessary to test at concentrations above 180 mg/L in another test as the maximum recommended test concentration in the test guideline (OECD 202 & Method C2 of Commision Directive 92/69/EEC) is 100 mg/L at which 25% immobilisation was observed in the definitive test. Due to the flat response observed in the definitive test immobilisation was observed down to concentrations of 18 mg/L and hence the NOEC after 48h exposure is 10 mg/L.
- Results with reference substance (positive control):
- A positive control conducted approximately every six months used potassium dichromate as the reference material. Daphnia magna was exposed to an aqueous solution of the reference material at concentrations of 0.32, 0.56, 1.0, 1.8 and 3.2 mg/l for 48 hours at a temperature of approximately 20°C under static test conditions. Immobilisation and any adverse reactions to exposure were recorded after 3, 24 and 48 hours.
Any other information on results incl. tables
Cumulative Daphnia Immobilisation Data in the Definitive test
At 24h:
Control 0%
1.8 mg/L 0%
3.2 mg/L 0%
5.6 mg/L 0%
10 mg/L 0%
18 mg/L 0%
32 mg/L 0%
56 mg/L 15% (3/20)
100 mg/L 15% (3/20)
180 mg/L 20% (4/20)
At 48h:
Control 0%
1.8 mg/L 0%
3.2 mg/L 0%
5.6 mg/L 0%
10 mg/L 0%
18 mg/L 5% (1/20)
32 mg/L 5% (1/20)
56 mg/L 20% (1/20)
100 mg/L 25% (5/20)
180 mg/L 35% (7/20)
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The acute toxicity of the test substance to the freshwater invertebrate Daphnia magna has been investigated and gave a 48h EC50 value of greater than 180 mg/L. The No Observed Effect Concentration at 48h was 10 mg/L.
- Executive summary:
Introduction.
A study was performed to assess the acute toxicity of the test material to Daphnia magna. The method followed that described in the OECD Guidelines for Testing of Chemicals (April 2004) No 202, "Daphnia sp, Acute Immobilisation Test" referenced as Method C.2 of Commission Directive 92/69/EEC (which constitutes Annex V of Council Directive 67/548/EEC).
Methods.
Following a preliminary range-finding test, twenty daphnids (2 replicates of 10 animals) were exposed to an aqueous solution of the test material at concentrations of 1.8, 3.2, 5.6, 10, 18, 32, 56, 100 and 180 mg ai*/l for 48 hours at a temperature of 21.1°C to 21.7°C under static test conditions. The number of immobilised Daphnia were recorded after 24 and 48 hours.
Results and Conclusion
The 48 -hour EC50 for the test material to Daphnia magna based on nominal test concentration was greater than 180 mg/l. The no observed efect concentration was 10 mg/l.
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.
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