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EC number: 211-471-9 | CAS number: 646-25-3
- 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:
- 2008-06-25 to 2008-06-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- The analytical monitoring was conducted at three test concentrations (1.5, 16.5 and 80 mg/l) at the start (0h) and at the end of the test (48h). After
48h, 2 ml-samples were taken both from additional test vessels (without Daphnia) and from the test vessels with Daphnia to check the influence of the test organisms. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: a stock solution of 80 mg/l was prepared with dilution water; seven test solutions with concentrations ranging from 0.7 to 80 mg/l were
were prepared from this stock solution
- Controls: dilution water - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: Straus
- Source: from a clone breeding at the German Federal Environmental Agency (UBA), Berlin
- Age at study initiation: 4-23 h
- Method of breeding:
- Feeding during test: no
ACCLIMATION
- Acclimation period: 4 h at 20 +/- 2 °C in the dark
- Acclimation conditions: same as test - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Test temperature:
- 20-21 °C
- pH:
- control: 7.8 - 8.5
0.7 mg/l: 7.9 - 7.9
1.5 mg/l: 7.9 - 8.2
3.4 mg/l: 8.0 to 8.2
7.5 mg/l: 8.0 ot 8.1
16.5 mg/L: 8.1 to 8.3
36.4 mg/L: 8.0 to 8.7
80 mg/L: 9.2 to 8.2 - Dissolved oxygen:
- control: 7.6 to 8.0 mg/l
0.7 mg/l: 7.6 to 8.0 mg/l
1.5 mg/l: 7.6 to 7.9 mg/l
3.4 mg/l: 7.7 to 8.1 mg/l
7.5 mg/l: 7.7 to 8.0 mg/l
16.5 mg/L: 7.7 to 8.0 mg/l
36.4 mg/L: 7.6 to 7.9 mg/l
80 mg/L: 7.7 to 8.0 mg/l - Nominal and measured concentrations:
- A: 0.7, B: 1.5, C: 3.4 ,D: 7.5, E: 16.5, F: 36.4 and G: 80.0 mg/l (nominal)
B: 1.46, E: 16.1, G: 78.8 mg/l (measured, 0 h)
B: 1.47, E: 16.3, G: 79.4 mg/l (measured, 48 h, with animals)
B: 1.5, E: 16.6, G: 85.7 mg/l (measured, 48 h, without animals) - Details on test conditions:
- TEST SYSTEM
- Test vessel: 50 ml-beakers, filled with 20 ml test medium each
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- ISO test water
EFFECT PARAMETERS MEASURED:
- immobility at 0 and 48 hours
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.2
- Range finding study: yes (non-GLP - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 7.71 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 6.23-9.55
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 20.1 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 14.98-26.96
- Duration:
- 24 h
- Dose descriptor:
- EC10
- Effect conc.:
- 3.88 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 2.76-5.45
- Duration:
- 48 h
- Dose descriptor:
- EC10
- Effect conc.:
- 7.14 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 4.20-12.11
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 3.4 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- 80 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Behavioural abnormalities: no
- Mortality of control: no
- Other adverse effects control: no
At the higher test concentrations, more immobilised Daphnia were observed after 24h than after 48h. The results indicate that apparently the Daphnia were temporarily intoxicated at 36.4, 16.5 and 7.5 mg/l. After 48 h, recovery took place, explaining the higher 48h-EC50. - Results with reference substance (positive control):
- - Results with reference substance valid
- EC50: 1.12 mg/l (CL, 95 %: 1.02-1.24 mg/l) - Reported statistics and error estimates:
- EC10-, EC20- and EC50-values (including confidence limits) as well as the concentrations demonstrating no effect (NOEC) were calculated for both
assessments (24 and 48h) using the statistical software ToxRat (ToxRat solutions GmbH, Alsdorf) - Validity criteria fulfilled:
- yes
- Conclusions:
- The EC50 (48h) based on nominal concentrations was determined as 20.1 mg/L indicating that the test substance may be harmful to aquatic invertebrates.
- Executive summary:
The 48-h acute toxicity of decamethylenediamine to Daphnia magna was studied under static conditions according to OECD TGD 201. Daphnids were exposed to the test item at nominal concentrations of 0.7, 1.5, 3.4, 7.5, 16.5, 36.4 and 80.0 mg/l for 48 h. Immobilisation was observed.
The 48h-EC50 was 20.10 mg/L.
This study was assessed as "reliable without restrictions".
Reference
The recovery rates [%] for the test item in the test solutions B (1.5 mg/l), E (16.5 mg/l) and G (80 mg/l) were as follows:
At the start of the test (0h):
B: 97.3%, E: 97.6%, G: 98.5%
At the end of the test (48h):
B: 98.0%, E: 98.8%, G: 99.3% (with animals)
B: 100.0%, E: 100.6%, G: 107.1% (wihtout animals)
Description of key information
The 48-h acute toxicity of decamethylenediamine to Daphnia magna was studied under static conditions according to OECD TGD 201. Daphnids were exposed to the test item at nominal concentrations of 0.7, 1.5, 3.4, 7.5, 16.5, 36.4 and 80.0 mg/l for 48 h. Immobilisation was observed. The 48h-EC50 was 20.10 mg/L.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- 20.1 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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