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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 204-709-8 | CAS number: 124-68-5
- 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
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Not applicable
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Remarks:
- no analytical follow-up
- Qualifier:
- according to guideline
- Guideline:
- other: Methods of Acute Toxicity Tests with Fish, Macroinvertebrates and Amphibians. Stephan, C. E., Chairman. 1975. Committee on Methods for Toxicity Tests with Aquatic Organisms. U.S. EPA, Ecol. Res. Ser. 660/3-75009.
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
Not applicable - Analytical monitoring:
- no
- Details on sampling:
- - Concentrations:0, 32, 56, 100, 180, 320 and 560 mg/l, with ten fish per concentration. Before the test concentrations were prepared, the standard was allowed to warm to room temperature (22°C). The test concentrations were obtained by transferring appropriate aliquots of a working solution directly to the test chambers. The working solution was prepared in deionized water,
- Vehicle:
- no
- Details on test solutions:
- Prepared in deionized water. Test concentrations were prepared based on the total compound.
- Test organisms (species):
- Lepomis macrochirus
- Details on test organisms:
- Bluegill sunfish were obtained from a commercial supplier, and held in culture tanks with a 16-hour light cycle, and acclimated for 14 days prior to exposure to the test material. Fish received a standard commercial fish food until 48 hours prior to testing, at which time feeding was discontinued. The fish had a mean weight of 0.21 grams and a mean standard length of 22 mm.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Post exposure observation period:
- Not applicable
- Hardness:
- 45 mg/L as CaCO3
total alkalinity was 25 mg/L CaCO3 - Test temperature:
- 21-23C
- pH:
- 7.0
- Dissolved oxygen:
- 8.8 mg/L
- Nominal and measured concentrations:
- Dose levels for the definitive assay were 32-560 mg/L in logarithmic series. Concentrations are reported based on nominal dose.
Dose levels for the definitive 96-hour study were set in a 72-hour range-finding test at 1, 10, 100, 560, 1000 mg/L. - Details on test conditions:
- The static bioassay was conducted in 5-gallon glass vessels containing 15 liters of reconstituted water (48mg NaHCO3, 30mg CaSO4, 30mg MgSO4, and 2mg KCl). Vessels were kept in a water bath at 21-23C, and the fish were acclimated to the dilution water and test temperature, and fasted for 48 hours prior to testing.
- Reference substance (positive control):
- yes
- Remarks:
- Antimycin A
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 190 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 150-250 mg/L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: mortality and sublethal effects
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- 220 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 170-280 mg/L
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 220 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 170-280 mg/L
- Details on results:
- The LC50 data was reported as follows:
AMP 24-hour LC50 = 220 (170-280) mg/L
AMP 48-hour LC50 = 220 (170-280) mg/L
AMP 96-hour LC50 = 190 (150-250) mg/L
Loss of equilibrium and surfacing was noted in some fish at 320 mg/L. - Results with reference substance (positive control):
- The LC50 data was reported as follows:
Antimycin A 24-hour LC50 = 0.000056 mg/L
Antimycin A 48-hour LC50 = 0.000037 mg/L
Antimycin A 96-hour LC50 = 0.000028 mg/L - Sublethal observations / clinical signs:
The LC50 was determined with the Probit method
- Validity criteria fulfilled:
- not specified
- Remarks:
- There is no information on the stability of the test subtance. No mortality was observed in the control.
- Conclusions:
- In Lepomis macrochirus, 96h NOEC and LC50 values were 100 and 190 mg/L, resp., expressed in test material containing 5% water. This corresponds to NOEC and LC50 values of 95 and 180 mg active substance/L, resp. All values are nominal (no analytical follow-up).
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Not applicable
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Remarks:
- no analytical follow-up
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EPA OPPTS 850.1075 (Freshwater and Saltwater Fish Acute Toxicity Test)
- Deviations:
- yes
- Remarks:
- A saltwater species was tested. No analytical verification of the test concentrations
- Principles of method if other than guideline:
- The test protocols are appended to the report.
- GLP compliance:
- no
- Analytical monitoring:
- no
- Vehicle:
- not specified
- Details on test solutions:
- Concentrations were prepared in sea-water.
- Test organisms (species):
- Pleuronectes platessa
- Details on test organisms:
- - Length at study initiation (length definition, mean, range and SD): mean length of 63.2mm
- Weight at study initiation (mean and range, SD): mean weight of 4.1g
- Nb of fish per vessel : 20
- Source: Tor Bay - Test type:
- semi-static
- Water media type:
- saltwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- not reported
- Test temperature:
- Nominal temperature of the test solution was 15C (14.4-15C during the test).
- pH:
- 8.1-10.3
- Dissolved oxygen:
- 7.0-8.2 mg/L
- Salinity:
- 34.76-34.82 o/oo
- Nominal and measured concentrations:
- Nominal concentrations tested were 100, 320, 560, 1000 mg/L.
- Details on test conditions:
- In a 96-hour, semi-static seawater test system, the toxicity of AMP-95 to Plaice was studied. Fish (20 per dose level, mean weight of 4.1g and mean length of 63.2mm) were placed in 18L glass vessels containing 10L of the test solution. The pH of the dilution seawater was 8.08-8.14, and salinity was 34.76-34.82 o/oo. Concentrations tested were 100, 320, 560, 1000 mg/L.
- Reference substance (positive control):
- no
- Duration:
- 24 h
- Dose descriptor:
- LC50
- Effect conc.:
- 231 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 138-385 mg/L
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 184 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 31-340 mg/L
- Duration:
- 72 h
- Dose descriptor:
- LC50
- Effect conc.:
- 184 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 31-340 mg/L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 184 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CL: 31-340 mg/L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Reported statistics and error estimates:
- The LC50 were determined based on the Probit model.
- Sublethal observations / clinical signs:
Not applicable
- Validity criteria fulfilled:
- yes
- Remarks:
- No mortality was observed in the control, the DO ranged between 7.2-8.4 mg/L and the substance is not hydrolysable.
- Conclusions:
- In marine fish Pleuronectes platessa, 96h NOEC and LC50 values were 100 and 184 mg/L, resp., expressed in test material containing 5% water. This corresponds to NOEC and LC50 values of 95 and 175 mg active substance/L, resp. All values are nominal (no analytical follow-up).
Referenceopen allclose all
Description of key information
- 95 and 180 mg/L, resp. over 96h in freshwater fish Lepomis macrochirus;
- 320 and 331 mg/L, resp. over 48h in freshwater fish Leuciscus idus melanotus;
- 95 and 175 mg/L, resp. over 96h in marine fish Pleuronectes platessa.
All available studies evidence negligible acute toxicity to fish. NOEC and LC50 values were:
All values are nominal (no analytical follow-up) and expressed as mg active substance/L. Reported nominal LC50/NOECs were converted into active substance equivalents taking into account the water content of the test items. Measured concentrations in two 2014 algae studies demonstrated the stability in both fresh- and saltwater media over 96h.
The data evidence similar sensitivity of freshwater and marine species.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Dose descriptor:
- LC50
- Effect concentration:
- 180 mg/L
Marine water fish
Marine water fish
- Dose descriptor:
- LC50
- Effect concentration:
- 175 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.
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.