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Reaction mass of lithium sodium 5-amino-3-{[4-(2-{4-[(7-amino-1-hydroxy-3-sulfo-2-naphthyl)diazenyl]-2-sulfophenyl}vinyl)-3-sulfophenyl]diazenyl}-4-hydroxynaphthalene-2,7-disulfonate 2,2'-(methylimino)diethanol (1:1) and 3,3'-[vinylenebis[(3-sulpho-p-phenylene)azo]]bis[6-amino-4-hydroxynaphthalene-2-sulphonic] acid, lithium sodium salt, compound with 2,2'-(methylimino)diethanol and 3,3'-[vinylenebis[(3-sulpho-p-phenylene)azo]]bis[5-amino-4-hydroxynaphthalene-2,7-disulphonic] acid, lithium sodium salt, compound with 2,2'-(methylimino)diethanol
EC number: 916-916-7 | 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
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Version / remarks:
- (2008)
- Deviations:
- no
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- (2004)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Concentration of 100 mg/L was measured at 0 and 48 hours; and concentration of 0 mg/L at 48 hours only.
- Sample storage conditions before analysis: Routinely, the samples were analysed immediately. Only in exceptional cases, they were stored overnight deep frozen and protected from light. - Vehicle:
- no
- Details on test solutions:
- To produce the only test item concentration, 284.0 mg of the test item were weighed out and were added directly to 1 litre of dilution water and stirred for 24 h on a magnetic stirrer. The pH was measured to be 8.1.
50 mL of the solution were taken and 0.5 mL of dilution water containing 10 daphnids were given to each replicate. For the test item concentration and the control 2 replicates were prepared. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- - Name: Daphnia magna STRAUS, parthenogenetic females
- Source: Strain of Bundesgesundheitsamt Berlin
- Maintenance and Acclimatisation: A population of parthenogenetic females of synchronized age structure has been maintained for more than 15 years in the test facility under constant temperature conditions (20 +/- 1 °C) at a 16 : 8 hour light-dark photoperiod (light intensity:
< 20 µE x m-2 x s-1). The culture water (so-called 'M4 medium') was partly renewed once a week. The Daphnia were exclusively fed unicellular green algae (Desmodesmus subspicatus) 'ad libitum'. Mortalities of parent Daphnia during the culture period were recorded daily in a semi-quantitative way. The neonates were separated from their parent Daphnia by filtration prior to the acute test. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Hardness:
- 16 °dH (= 286 mg/L CaCO3)
- Test temperature:
- 19.4 - 19.9 °C measured at each test vessel at the beginning and thr end of the test
- pH:
- 8.0 - 8.1 measured at each test vessel at the beginning and thr end of the test
- Dissolved oxygen:
- 7.5 - 9.1 mg/L with 90 - 99 % saturation measured at each test vessel at the beginning and thr end of the test
- Nominal and measured concentrations:
- 100 mg/L (nominal) plus control
The results are expressed in terms of nominal concentrations concentrations at 48 h. Effective concentrations correspond to 104.1 % of nominal values at 0 hours and to 99.9 % of nominal values at 48 hours. - Details on test conditions:
- Pretreatment of test item and preparation of test item concentrations:
To produce the only test item concentration, 284.0 mg of the test item were weighed out and were added directly to 1 litre of dilution water and stirred for 24 h on a magnetic stirrer.
The pH was measured to be 8.1.
50 mL of the solution were taken and 0.5 mL of dilution water containing 10 daphnids were given to each replicate. For the test item concentration and the control 2 replicates were prepared.
Test system:
- Test vessels: 100 mL glass beakers covered with watch glasses holding 10 neonates in 50 mL of test medium
- Experimental design: 1 test concentration plus 1 control, 10 neonates per vessel, 2 replicates per concentration/control, no feeding during the exposure period, static system
- Method of initiation: neonates were placed in prepared media
- Photoperiod: 16 h light : 8 h dark
- Temperature of incubation unit: 20.2 to 20.3°C
- Aeration: none
- Test item concentration: 100 mg/L (active ingredient)
- Method of administration: direct weighing
- Medium renewal: none
- Duration of exposure: 48 hours
- Criteria of effects: The criterion of adverse effects used in this study was the item-induced alteration of the normal mobility behaviour and the loss of locomotory actions of the neonates, observed at 48 hours. - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- The test medium exhibited a too strong colouration to observe immobility and behaviour of the daphnids at 24 hours. To verify immobilisation and abnormalities at 48 hours daphnids were placed in clear dilution medium.
No toxic effects against Daphnia were observed at a limit test concentration of 100 mg/L of the test item. - Validity criteria fulfilled:
- yes
- Remarks:
- (- The immobilisation and other abnormalities in the controls did not exceed 10 % by the end of the test. - The dissolved oxygen concentration remained above 3 mg/L throughout the exposure period.)
- Conclusions:
- Daphnia magna was exposed under static conditions for 48 hours to one concentration (100 mg/L) of the test substance. No toxic effect was obseved.
- Executive summary:
In order to test acute toxicity to invertebrates of the substance Daphnia magna was expoded to the test solution of one nominal concentration of the test substance (100 mg/L) and blank control solution for a period of 48 hours under static conditions. The test medium exhibited a too strong colouration to observe immobility and behaviour of the daphnids at 24 hours. To verify immobilisation and abnormalities at 48 hours daphnids were placed in clear dilution medium and recorded at 24 and 48 hours. The measured concentrations confirmed that deviation from the nominal concentration was less than 20 % (measured concentration were in the range of 99.9 - 104.1 % of nominal concetrations). No toxic effect and abnormal behavior were obsevered. This toxicity study is classified as acceptable and satisfies the guideline requirements for the acute Daphnia study.
Reference
Description of key information
Daphnia magna was exposed under static conditions for 48 hours to one concentration (100 mg/L) of the test substance. No toxic effect was obseved.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- > 100 mg/L
Additional information
In accordance with REACH Regulation, Art. 3, and ECHA "Guidance for identification and naming of substances under REACH and CLP" v1.2, March 2012, substances have to be separated from solvents if this is not affecting the stability of the substance or changing its composition.
In this case, separation of water would only be possible by thermical damaging of the substance. Furthermore, it was not possible to spray dry the pigment solution as it stuck to and partly melted on the conus dryer.
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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