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EC number: 203-607-0 | CAS number: 108-69-0
- 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:
- Dec.24, 1997 - March 91, 1998
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- Study on behalf of competent authorities of Japan
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- 1984
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
The test solution was prepared by diluting 1000 mg of the test substance in 1000 mL of pure water (concentration of test substance: 1000 mg/L). For the test solution, the following volume of the test substance stock solution was taken and diluted to 5.0 g/L with dilution water.
A stock solution containing 100 mg/ml of the test substance was prepared. After adding the test substance stock solution according to each concentration, each test solution was prepared. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Age at study initiation (mean and range, SD): juvenile daphnia within 24 hours of birth
- Stage and instar at study initiation: juveniles
- Source: National Institute for Environmental Studies on July 18, 1995.
- Breeding density: Juveniles: 35 or 40 / 3L; Adults 35 / 3L
- Feeding
- Food type: Chlorella vulgaris
- Amount: 0.15 mg C per Daphnia magna/day
- Feeding during test: no
METHOD FOR PREPARATION AND COLLECTION OF EARLY INSTARS OR OTHER LIFE STAGES, INCLUDING CULTURING CONDITIONS:
Adult females of sufficient size to be visually healthy with juvenile Daphnia magna were selected from those in the passages and transferred to a separately prepared beaker.
The next day, the produced larvae were divided into another beaker. The next day, the produced juveniles were divided into another beaker.
At the beginning of the fourth week, on the day before the start of exposure, the larvae were removed at least twice a week.
On the day before the start of the fourth week of exposure, adult females with juveniles in the broodstock were selected from batches that had not produced dormant eggs or males and had less than 5% mortality in the previous two weeks. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 63 mg/L (CaCO3)
- Test temperature:
- 20±1 ℃
- pH:
- 8.1
- Nominal and measured concentrations:
- control, 1.00, 1.30, 1.70, 2.30, 3.00, 5.50, 13.0 and 30.0 mg/L (ratio 1.3 - 2.4)
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Test container
- Type (delete if not applicable): closed with Teflon sheet
- Material, size, headspace, fill volume: glass, 100 mL
- Volume of solution: 100 ml test solution
- No. of organisms per vessel: 5 (20 per concentration)
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
OTHER TEST CONDITIONS
- Adjustment of pH:
- Photoperiod: 16h light/8h dark
- Light intensity: 1200 lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
RANGE-FINDING STUDY
two preliminary tests
- Test concentrations: 0.1, 1.00, 10.0, 30.0, 100 mg/L and 1.00, 3.00, 10.0 , 30.0 and 100 mg/L - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate The EiC50 was 0.23 mg/kg for 48 hours.
- Duration:
- 48 h
- Dose descriptor:
- LC100
- Effect conc.:
- 5.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.3 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 2.2 mg/L
- 95% CI:
- >= 2.02 - <= 2.4
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- Since all measured concentrations of the test substance were within ±20% of the set value, the set value was used for the calculation of each effect concentration.
No Daphnia magna was observed floating on the surface of the water in the control area. - Reported statistics and error estimates:
- The swimming inhibition rate (%) was calculated from the number of Daphnia magna swimming inhibition in each concentration zone and the number of individuals tested (20), and the half swimming inhibition concentration (Eic50) was calculated by the Probit method.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The median immobilisation concentration (EC50) after 48 hours was determined to be 2.2 mg/L.
- Executive summary:
A GLP- acute immobilization test (static) of 3,5-xylidine on Daphnia magna in a 48-hour exposure was carried out in accordance with the acute immobilization test described in "Methods of Tests pertaining to New chemical Substances, Etc" and comparable to OECD Guideline 202.
20 daphnids per concentration area (5 daphnids/ container) were exposed to the test substance at static conditions and at test concentrations of 0.1, 1.00, 10.0, 30.0, 100 mg/L and 1.00, 3.00, 10.0 , 30.0 and 100 mg/L (nominal). The median immobilisation concentration (EC50) after 48 hours was determined to be 2.2 mg/L and the NOEC was determined to be 1.3 mg/L.
Reference
Description of key information
OECD 202, GLP, Daphnia magna, static: EC50(48h) 2.2 mg/L (nominal)
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- 2.2 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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