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EC number: 277-274-5 | CAS number: 73070-48-1
- 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 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
- Study period:
- 23/01/2006 - 16/03/2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- other: ISO 14669:1999 (E) - Draft method
- Deviations:
- not specified
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Details on sampling:
- - Concentrations: Rangefinding concentrations: 0, 2.0, 20.0, 200.0 mg/L test material, 0, 20.0, 35.6, 63.3, 112.5, 200.0 mg/L
- Sampling method: Percentage immobilisation in population - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Test material dissolved in seawater (1 g/ L) and aliquots taken from stock to make range of lower concentrations
- Controls: 1 mortality control (0 mg/L test material) and 1 positive control (reference substance - 3, 5 - dichlorophenol) for each time point (24 and 48 hours).
- Evidence of undissolved material (e.g. precipitate, surface film, etc.): No, test substance was soluble in seawater for maximum concentration tested. - Test organisms (species):
- other aquatic crustacea: Acartia tonsa
- Details on test organisms:
- TEST ORGANISM
- Common name: Acartia tonsa
- Batch number: AT06009
- Source: Guernsey Sea Farms, Guernsey
- Age of parental stock: Unknown, test organisms used were 13 - 15 days olds.
- Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Remarks on exposure duration:
- Measurements taken at 24 and 48 hours
- Test temperature:
- Test condition not provided.
Seawater on arrival was 12 °C and it was stored at 20 (+-2) °C prior to use - pH:
- Test condition not provided.
Seawater on arrival was pH 7.99 - Dissolved oxygen:
- Test condition not provided.
Seawater on arrival had a 100 % dissolved oxygen level. - Salinity:
- Test condition not provided.
Seawater salinity was 33.2 g/L on arrival. - Nominal and measured concentrations:
- Nominal test substance concentrations, 0, 20, 35.6, 63.3, 112.5, 200.0 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel volume: At least 5 mL
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Guernsey Sea Farms
- Alkalinity: pH 7.99 (on arrival)
- Salinity: 33.2 g/L (on arrival)
- Intervals of water quality measurement: at beginning and end of the test, not stated in the study
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : mortality for 24 and 48 hours
RANGE-FINDING STUDY
- Test concentrations: 0, 2.0, 20.0, 200.0 mg/L test material
- Results used to determine the conditions for the definitive study: Yes - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- 120.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 70.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 63.3 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- 112.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Results with reference substance (positive control):
- - Results with reference substance valid?
Information not provided
- Relevant effect levels: LC50, NOEC and LOEC
- Limit test: Yes, only 1.0 mg/L tested - Validity criteria fulfilled:
- yes
- Conclusions:
- The LC50 for 48 hours was 70.2 mg/L and for 24 hours it was 120.5 mg/L. The NOEC for 48 hours was 63.3 mg/L and the LOEC for 48 hours was 112.5 mg/L
- Executive summary:
This study assesses the actue toxicity for 25% M-528 -7 (W/W) neutralised with DEA in deionised water for marine invertebrates. 25% M-528 -7 (W/W) was identified as the registered substance. The study is performed in compliance with GLP and according to the method ISO 14669:1999 guideline. All validity criteria were met. The test organism used was Acartia tonsa and the test was performed in saltwater (seawater). A rangefinding test was performed using the concentrations 0, 2.0, 20.0 and 200.0 mg/L to determine a definitive test range. The definitive test used a range of nominal concentrations 0, 20.0, 35.6, 63.3, 112.5 and 200.0 mg/L test substance. This range was produced by dissolving the test material in seawater (1.0 g/ L) from which aliquots were taken to make dilutions. The results of the definitive test were LC50 for 24 hours was 120.5 mg/L and for 48 hours was 70.2 mg/L, the NOEC for 48 hours was 63.3 mg/L and the LOEC for 48 hours was 112.5 mg/L. The definitive test contained data points for 24 and 48 hours per concentration, with one replicate each. Two mortality controls (0 mg/L test substance) were included per time period with 0% and 3% immobilisation/mortality at 24 and 48 hours, respectively. Two positive controls were included (reference substance, 3,5 - dichlorophenol at 1mg/L) per time period with 0% and 55% immobilisation at 24 and 48 hours, respectively
Reference
Description of key information
This study assesses the acute toxicity for 25% M-528 -7 (W/W) neutralised with DEA in deionised water for marine invertebrates. 25% M-528 -7 (W/W) was identified as the registered substance, The study is performed in compliance with GLP and according to the method ISO 14669:1999 guideline. All validity criteria were met. The test organism used was Acartia tonsa and the test was performed in saltwater (seawater). A rangefinding test was performed using the concentrations 0, 2.0, 20.0 and 200.0 mg/L to determine a definitive test range. The definitive test used a range of nominal concentrations 0, 20.0, 35.6, 63.3, 112.5 and 200.0 mg/L test substance. This range was produced by dissolving the test material in seawater (1.0 g/ L) from which aliquots were taken to make dilutions. The results of the definitive test were LC50 for 24 hours was 120.5 mg/L and for 48 hours was 70.2 mg/L, the NOEC for 48 hours was 63.3 mg/L and the LOEC for 48 hours was 112.5 mg/L. The definitive test contained data points for 24 and 48 hours per concentration, with one replicate each. Two mortality controls (0 mg/L test substance) were included per time period with 0% and 3% immobilisation/mortality at 24 and 48 hours, respectively. Two positive controls were included (reference substance, 3,5 - dichlorophenol at 1mg/L) per time period with 0% and 55% immobilisation at 24 and 48 hours, respectively
Key value for chemical safety assessment
Marine water invertebrates
Marine water invertebrates
- Effect concentration:
- 70.2 mg/L
Additional information
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.
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