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EC number: 270-335-7 | CAS number: 68425-15-0
- 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:
- 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- not specified
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- Sampled for analysis at 0 and 48 hours.
- Vehicle:
- no
- Details on test solutions:
- Preparation: Since TPS 32 is poorly soluble in water; a saturated solution was prepared by vigorously mixing: 100 mg of TPS 32 with dilution water during 23 hours at 20°C (preliminary test) and 2 mg of TPS 32 with dilution water during 68 hours at 20°C (definitive test). After this saturation period, the saturated solution was filtered with a HV 0.45 µm filter. Vehicle, solvent: Ultrapure water. Dilution water was prepared in the laboratory using pure water and salts according to ISO 6341.
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Strain: Daphnia magna straus strain 5 or A. Source/supplier: Breeding colony was realized in Elendt M7 medium in the laboratory, organisms were selected by sieving. Breeding method: Not available. Age: Less than 24 hours. Feeding: Microscopic algae Raphidocelis subcapitata. Pretreatment: No. Feeding during test: No. Control group: Yes.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
- Post exposure observation period:
- No
- Hardness:
- 200 ± 20 mg/L as CaCO3
- Test temperature:
- 20 ± 1°C
- pH:
- 8.2 ± 0.2
- Dissolved oxygen:
- 9.2 ± 0.3 mg/L
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Series of approximately dilutions of the dissolved item from 6.25% to 100 % . Concentrations: 6.25, 12.5, 25, 50, 100 nominal concentration (% vol), forming a geometric progression with a factor of 2. Measured concentrations were not available, because the analytical method did not allow the determination of the test substance concentration.
- Details on test conditions:
- Type and source of exposure medium: ultrafiltered water with carbon exchange. Test vessel: 250 mL glass flasks. No of organisms per vessel: 5. No of replicates per concentration: 4. Photoperiod: Incubation of test flasks in darkness.
- Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- NOEC
- Effect conc.:
- < 0.1 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- dissolved
- Basis for effect:
- mortality
- Remarks on result:
- other: Limit of quantification
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- < 0.1 mg/L
- Nominal / measured:
- meas. (not specified)
- Conc. based on:
- dissolved
- Basis for effect:
- mortality
- Remarks on result:
- other: Limit of quantification
- Details on results:
- An EC50 was not reported. This may be due to the fact that the test item was not detected at the limit of detection and quantification of the analytical technique due to its very low solubility. A 5% effect was observed at 24hr and 48 hours but this is considered to be not significant as an immobilisation up to 10% is permitted by the TG in the blank control. The limit of detection and quantification for the analytical technique employed was 0.03 and 0.01 mg/l, respectively.
- Results with reference substance (positive control):
- The sensitivity of the test organism is confirmed by a toxicity test with Potassium dichromate periodically, EC50/24h =1.1mg/l.
- Reported statistics and error estimates:
- No data reported
- Validity criteria fulfilled:
- no
- Remarks:
- The analytical method used in the test did not allow the determination of the substance concentration as the solubility of the substance in the test medium was below the limit of quantification. The stability of the test substance was also not checked.
- Conclusions:
- An acute EC50 value could not be calculated for polysulfides, di-tert-dodecyl due to its very low solubility in water and hence the low exposure to the this substance. At the solubility limit of the test substance, no significant immobilization if the test organisms was recorded after 24 and 48 hours. Thus the polysulfides, di-tert-dodecyl was not toxic for daphnia at the maximal exposure concentration corresponding to the solubility limit of the polysulfides, di-tert-dodecyl in the test medium. The solubility/dispersibility limit of polysulfides, di-tert-dodecyl in the test medium was below the range of quantification ( i.e., 0.1 mg/l) and above the detection limit (i.e.0.02 mg/l) of the analytical method, therefore 0.02 mg/l < Solubility limit <0.1 mg/l.
- Executive summary:
Thiebaud (1998) is a 48 hour, static, freshwater, GLP-compliant test on Daphnia magna, follows EU Method C2. The results no significant toxicity to aquatic invertebrates at the limit of solubility (which is below the limits of analytical detection). The study is considered reliable and suitable for use for this endpoint.
Reference
Nominal Measured Immobile (%)
conc Init Final
% mg/l 24 hr 24 hr 48 hr
100 <LQ <LQ 5 5
50 <LD <LD 0 5
25 NA NA 0 0
12.5 NA NA 5 5
6.25 NA NA 0 0
Description of key information
An acute EC50 value could not be calculated for polysulfides, di-tert-dodecyl due to its very low solubility in water and hence the low exposure to the substance. At the solubility limit, no significant immobilization was recorded at 48 hours. Thus the substance was not toxic to daphnia at the maximal exposure concentration (the solubility limit). The solubility/dispersibility limit was below the range of quantification (0.1 mg/l) and above the detection limit (0.02 mg/l) of the analytical method, therefore 0.02 mg/l < solubility limit <0.1 mg/l.
Key value for chemical safety assessment
Additional information
Thiebaud (1998) is a 48 hour, static, freshwater, GLP-compliant test on Daphnia magna, follows EU Method C2. The results indicate that this substance is not significantly toxic to aquatic invertebrates at the limit of solubility (which is below the limits of analytical detection). The study is considered reliable and suitable for use for this endpoint.
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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