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EC number: 430-550-0 | CAS number: 1671-49-4
- 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:
- 10 May 1999 to 14 May 1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP compliant, guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Deviations:
- yes
- Remarks:
- One control was ouside the range 50 ± 10 mm in length at test termination. This is considered not to impact on the validity of the test
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: Samples were taken from the exposure concentrations and control.
- Sampling method: Samples were taken from the test medium at the start of the test, after 48 hours and after 96 hours. At the same times samples were also taken from the controls. Samples were taken from the approximate centre of the aquarium.
- Sample storage conditions before analysis: Not reported - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method:The test solutions were prepared by the direct addition of the required amounts of the test substance to each exposure vessel and thoroughly stirring for 24 hours.
- Controls: Yes, a single blank control of test water
- Evidence of undissolved material (e.g. precipitate, surface film, etc): A few white particles. - Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
- Details on test organisms:
- TEST ORGANISM
- Common name: Rainbow trout
- Strain: Not reported
- Source: Houghton Springs Fish Farm, Winterbourne Houghton, Blandford Forum, Dorset, DT11 0PD
- Age at study initiation (mean and range, SD): Not reported
- Control fish length at study termination: 39 - 52 mm, mean: 44 mm
- Control fish weight at study termination: 0.74 - 1.89 g, mean: 1.22 g
- Method of breeding: Not reported
- Feeding during test: No feeding from 24 hours prior to test
ACCLIMATION
- Acclimation period: 7 weeks
- Acclimation conditions (same as test or not): same as test, but with feeding and single large tank.
- Type and amount of food: Keystart 1200®
- Feeding frequency: Fed daily
- Health during acclimation (any mortality observed): No evidence of disease. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- 44.0 mg/L as CaCO3
- Test temperature:
- 14.2 ± 15.1°C measured daily
- pH:
- 7.24 - 7.57 measured daily
- Dissolved oxygen:
- 9.23 - 10.27 mg O2/L, measured daily
- Nominal and measured concentrations:
- See Table 1. Measured concentrations were in the range of 99 - 110 % of nominal, so results are reported as nominal concentrations
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Material, size, headspace, fill volume: Borosilicate glass vessels, 400 mm x 280 mm x 280 mm, max capacity 27.5 L, working volume 20 L.
- Aeration: Gentle aeration throughout test..
- Renewal rate of test solution (frequency/flow rate): Static test
- No. of organisms per vessel: 10 fish
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- No. of vessels per vehicle control (replicates): No vehicle control used
- Biomass loading rate: 0.61 g fish (wet weight)/L
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: tap water, passed through activated carbon, coarsely filtered, dechlorinated with sodium thiosulphate and salts added (as required) to maintain minimum hardness levels. Total hardness reduced by ion exchange
- Total organic carbon: Not reported
- Particulate matter: Not reported
- Metals: Not reported
- Pesticides: Not reported
- Chlorine: Free residual: <2 µg/L, Combined residual: <2 µg/L
- Alkalinity: 22.6 mg/L as CaCO3
- Ca/mg ratio: Not reported
- Conductivity: 204 µS cm-1 at 25°C
- Culture medium different from test medium: No
- Intervals of water quality measurement: Not reported
OTHER TEST CONDITIONS
- Adjustment of pH: None
- Photoperiod: 16L:8D with a 20 minute transition period
- Light intensity: Not reported
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Fish were observed after 24, 48, 72 and 96 hours for mortality and visible abnormalities.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.8
- Test concentrations: 10, 18, 32, 56, 100 mg/L - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- LC50
- Effect conc.:
- 70 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CI: 57-94 mg/L
- Duration:
- 72 h
- Dose descriptor:
- LC50
- Effect conc.:
- 61 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CI: 52-74 mg/L
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- 59 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: 95% CI: 49-70 mg/L
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 18 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: all symptoms observed
- Details on results:
- - Behavioural abnormalities: Fish showed the following abnormailities: Quiescence, sounding, loss of balance, cessation of swimming .
- Observations on body length and weight: Not reported
- Other biological observations: Fish showed the following abnormailities: Weakness, dark discolouration.
- Mortality of control: No mortality in controls
- Other adverse effects control: No other adverse effects in controls
- Abnormal responses: No abnormal responses observed
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: Not applicable as test concentrations measured
- Effect concentrations exceeding solubility of substance in test medium: No - Reported statistics and error estimates:
- LC50s and 95% confidence intervals calculated by moving average angle
- Sublethal observations / clinical signs:
Table 2 Effects of the test subsance on the survival of Oncorhynchus mykiss
Nominal concentration (mg/L) Cumulative percentage mortality observed 24 hours 48 hours 72 hours 96 hours Dilution water control 0 0 0 0 10 0 0 10 10 18 0 0 0 0 32 0 0 0 0 56 20 20 30 40 100 60 90 100 100 LC50(mg/L) not calcuated 70 61 59 NOEC (mg/L) (all symptoms) not calcuated not calcuated not calcuated 18 - Validity criteria fulfilled:
- yes
- Conclusions:
- Based on nominal concentration, the 96-hour LC50 for rainbow trout (Oncorhynchus mykiss) was 59 mg/L and the 96-hour NOEC was 18 mg/L.
- Executive summary:
The acute toxicity of the test substance to rainbow trout (Oncorhynchus mykiss) was determined. In accordance with the guideline fish were exposed to a test item concentrations of 10, 18, 32, 56 and 100 mg/L, alongside a dilution water control. Based on nominal concentrations, the 96-hour LC50 was 59 mg/L and the 96 -hour NOEC was 18 mg/L.
Reference
Description of key information
LC50=59 mg/L, 96h, Oncorhynchus mykiss, static, OECD 203, Magor 1999
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Effect concentration:
- 59 mg/L
Additional information
The acute toxicity of the test substance to rainbow trout (Oncorhynchus mykiss) was determined. In accordance with the guideline, fish were exposed to test item concentrations of 10, 18, 32, 56 and 100 mg/L, alongside a dilution water control. Based on nominal concentrations, the 96-hour LC50 was 59 mg/L and the 96-hour NOEC was 18 mg/L. The study is considered to be reliable and adequate for the purposes of risk assessment, classification and labelling.
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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