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Diss Factsheets
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EC number: 821-749-7 | CAS number: 154581-97-2
- 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:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Results derived from a valid read across, with adequate and reliable documentation / justification.
- Justification for type of information:
- The read across justification is presented in the overall Aquatic Endpoint Summary because in that document long-term toxicity to aquatic invertebrates and toxicity to aquatic algae is also included. The corresponding documentation file is also attached there.
- Reason / purpose for cross-reference:
- read-across source
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.247 mg/L
- Remarks on result:
- other: Based on read across information
- Validity criteria fulfilled:
- yes
- Remarks:
- Justification for read across is presented in the overall aquatic endpoint summary.
- Conclusions:
- For Acalea an 48h-EC50 of 0.247 mg/L has been derived for Daphnia based on read across information from Hexyl Cinnamic Aldehyde.
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- from June 2003 to December 2004
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- The test is conducted following OECD 202 guidelines and under GLP rules however, use of a solvent led to use of concentrations which caused floaters potentially confounding the toxicological results. Nevertheless this study can be considered fit for risk assessment purposes.
- Justification for type of information:
- Information used for read across to Acalea. The study record of HCA from the LR registrant is copied here, who finally derived an EC50 value of 0.247 mg/l.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Nominal concentrations selected for this study were 0.13, 0.25, 0.50, 1.0 and 2.0 mg a.i./L.
Concentration of samples collected in the pretest period were approximately 34 to 67% of nominal concentration.
Concentration of samples collected during the test were approximately 35 to 72% of nominal concentration.
- Sampling method: the samples were collected from one test chamber of each treatment and control group 2 days prior to the start of the test after conditioning the diluter for three days. Stock solution samples were collected on the day prior to test initiation to confirm the concentrations being delivered to the diluter. Samples also were collected from alternating replicate test chambers in each treatment and control group at test initiation and termination to measure concentrations of the test substance. All test solution samples were collected at mid-depth and placed in glass vials.
- Sample storage conditions before analysis:samples were analyzed immediately without storage. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Cladoceran
- Strain: Daphnia Magna
- Source: from cultures maintained by Wildlife International, Ltd., Easton, Maryland
- Age at study initiation (mean and range, SD): less than 24h old
- Weight at study initiation (mean and range, SD): no data
- Length at study initiation (length definition, mean, range and SD): no data
- Valve height at study initiation, for shell deposition study (mean and range, SD): not applicable
- Peripheral shell growth removed prior to test initiation: not applicable
- Method of breeding: Adult Daphnids were cultured in water approximately at the same temperature used during the test. They were held for at least 22 days prior to collection of the juveniles for testing.
- Feeding during test
- Food type: the neonates were not fed during the test
- Amount: not applicable
- Frequency: not applicable
- Test type:
- flow-through
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 128 mg/L as CaCO3
- Test temperature:
- water temperatures were within 20 ± 1 ºC
- pH:
- measurements of pH ranged from 8.1 to 8.3
- Dissolved oxygen:
- dissolved oxygen concentrations remained ≥7.9 mg/L (88% of saturation)
- Salinity:
- 184 mg/L as CaCO3
- Nominal and measured concentrations:
- Concentrations as mg a.i./L
Nominal Concentration: 0.13; Measured Concentration: 0.0886 (0h) and 0.0796 (48h)
Nominal Concentration: 0.25; Measured Concentration: 0.159 (0h) and 0.150 (48h)
Nominal Concentration: 0.50; Measured Concentration: 0.358 (0h) and 0.353 (48h)
Nominal Concentration: 1.0; Measured Concentration: 0.622 (0h) and 0.562 (48h)
Nominal Concentration: 2.0; Measured Concentration: 0.690 (0h) and 0.690 (48h) - Reference substance (positive control):
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.36 - < 0.59 mg/L
- Nominal / measured:
- estimated
- Conc. based on:
- act. ingr.
- Remarks on result:
- other: 95% confidence limits were 0.084 to 0.59 mg a.i./L
- Details on results:
- Concentraion
Control - Validity criteria fulfilled:
- yes
- Conclusions:
- The test substance was tested in a 48h flow-through acute toxicity test with daphnia magna following OECD 202 guidelines. EC50(48h) was found to be 0.247 mg a.i./L based on measured concentrations. While physical effects may be the cause of some immobilisation observed (floaters found in the test at all concentrations except the control) a 48 h EC50 for this test was determined and considered acceptable to evaluate the acute toxicity of the substance on invertebrates
- Executive summary:
The Daphnia Magna was exposed to five concentrations of the test substance under flow-through conditions for 48 hours. Analysis of the test solutions at 0 and 48 hours indicated that the test substance was not stable in water, as evidenced by the measured concentrations that ranged from approximately 35 to 72% nominal.
Concentration response effects were observed in the study and while physical effects may be the cause of some immobilisation observed (floaters found in the test at all concentrations except the control) the EC50 obtained is believed to be acceptable for use in hazard assessment.
Based on the mean measured test concentrations, a 48 -hour EC50 value of 0.247 mg/L was calculated.
Referenceopen allclose all
Nominal (mg/L) | Measured Concentration (mg/L) | % Immobilisation 24 h | % Immobilisation 48 h |
0 | Control | 0 | 5 |
0 | Solvent Control | 0 | 0 |
0.13 | 0.084 | 0 | 5 |
0.25 | 0.15 | 0 | 35 |
0.5 | 0.36 | 0 | 40 |
1 | 0.59 | 10 | 100 |
2 | 0.69 | 60 | 100 |
Description of key information
For Acalea an 48h-EC50 of 0.247 mg/L has been derived for Daphnia based on read across information from Hexyl Cinnamic Aldehyde.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 0.247 mg/L
Additional information
The experimental information from the source is presented here. The read across justification is presented in the overall Aquatic Endpoint Summary.
Hexyl Cinnamic Aldehyde and its short-term toxicity to Daphnia (copied from the Lead Registrant):
"The Daphnia Magna was exposed to five concentrations of the test substance under flow-through conditions for 48 hours. Analysis of the test solutions at 0 and 48 hours indicated that the test substance was not stable in water, as evidenced by the measured concentrations that ranged from approximately 35 to 72% nominal.
Concentration response effects were observed in the study and while physical effects may be the cause of some immobilisation observed (floaters found in the test at all concentrations except the control) the EC50 obtained is believed to be acceptable for use in hazard assessment.
Based on the mean measured test concentrations, a 48 -hour EC50 value of 0.247 mg/L was calculated".
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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