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EC number: 203-063-4 | CAS number: 102-87-4
- 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 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:
- 2013-04-09- 2013-04-11
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Vehicle:
- no
- Details on test solutions:
- The acute immobilization study on Daphnia magna was performed according to the OECD Guideline for the Testing of Chemicals No. 202 (2004) [1] and the SOP/W/21.
The preliminary tests were performed to determine the range of concentrations to be used in the definitive test.
The tests were performed using the Elendt M7 medium as a diluent necessary to prepare the test concentrations. The medium was aerated prior to the beginning of the test. The daphnids were exposed in glass beakers with a capacity of 150 mL. The beakers were covered with transparent lids in order to minimize evaporation and to prevent accidental contamination. In the preliminary tests, the volume of the test concentration and the test medium for the control in every replicate was 50 mL. In the definitive test, the volume of the test each concentration and the test medium for the control in every replicate was 100 mL. Five individuals of Daphnia magna were used in each replicate; hence, there were 10 or 20 mL of the test solution per daphnid (the OECD Guideline No. 202 requires at least 2 mL) [1]. Each test concentration and the control were tested in four replicates. The daphnids were exposed for 48 hours. The tests were conducted in static design.
During the exposure, the daphnids were not fed. The tests were performed under a 16-hour light and 8-hour dark regime. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- The test organism, Daphnia magna Straus originated from the standard laboratory culture cultivated at the Institute of Industrial Organic Chemistry, Branch Pszczyna, Department of Ecotoxicology [SOP/W/67]. Only organisms up to 24 hours old (not first brood progeny) and in good physiological condition were used in the experiments. The sensitivity of the culture was monitored on a regular basis using a reference substance, potassium dichromate.
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 21.0 – 22.7 ° C
- pH:
- pH of the control: 7.23 – 7.27
- Dissolved oxygen:
- oxygen concentration in the control: 8.4 – 8.5 mg/L
- Nominal and measured concentrations:
- The WAFs prepared from a loading of 6.25, 12.5, 25, 50 and 100 mg/L used in the definitive test were determined based on the preliminary tests results.
In samples of fresh solutions the determined concentrations of the total organic carbon in the control and in the WAF of a loading of 6.25 mg/L and 12.5 mg/L were below LoQ value, in the WAF of a loading of 25 mg/L was 1.186 mg C/L, in the WAF of a loading of 50 mg/L was 1.375 mg C/L and in
the WAF of a loading of 100 mg/L was 2.340 mg C/L.
In the samples of 48-hour-old solutions, the determined concentrations of the total organic carbon in control and in the WAF of a loading of 6.25 mg/L and 12.5 mg/L were below LoQ value, in the WAF of a loading of 25 mg/L was 1.178 mg C/L, in the WAF of a loading of 50 mg/L was 1.508 mg C/L and in the WAF of a loading of 100 mg/L was 2.464 mg C/L. - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 55.7 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- 12.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- LC100
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 50 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Validity criteria fulfilled:
- yes
- Conclusions:
- The substance was tested according to OECD 202. After 48h the EC50 was determined to be EC50:55.7 mg/l.
- 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:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- Being a tridodecylamine and a tri-C8,10-amine, target and source substance are structurally very similar only differing slightly in the length of the alkyl chain. Thus, both target and source subtance have identical functional group(s), common precursor(s)/breakdown product(s) as well as common mechanism(s) of action.
- Reason / purpose for cross-reference:
- read-across source
- Vehicle:
- no
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 55.7 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- 12.5 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- LC100
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 50 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Conclusions:
- Based on data for a suitable read across substance, one can assume that Tridodecylamine is toxic to aquatic invertebrates.
Referenceopen allclose all
Description of key information
EC50(48h) = 55.7 mg/L (nominal) for immobilisation of Daphnia magna (OECD 202, read across)
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 55.7 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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