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EC number: 203-412-0 | CAS number: 106-58-1
- 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:
- 1996-03-26 - 1996-03-28
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Version / remarks:
- Directive 79/831/EEC, Annex V, Part C
- GLP compliance:
- yes
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): 1,4-Dimethylpiperazin
- Analytical purity: 99.7 %
- Lot/batch No.: Abl.-No. 32-1 659
- CAS No.: 106-58-1
- State of aggregation : fluid
- Purity of active ingredient : 99,7% (Analytical Report ZAX 961-00033)
- Impurities/ secondary components : 0,08% water (Analytical Report ZAX 961-00033)
- Stability : stable. Store at room temperature under nitrogen atmosphere
- Date of production : September 1994
- Solubiiity in water : mixable up to 10 g/L - Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 0 (control), 6.25, 25 and 100 mg/L
- Sampling method: At the start of the test (after 0 hours) samples from vessels which were not stocked with daphnids were analysed and at the end
of the test (after 48 h) samples from stocked and unstocked vessels were analysed.
- Sample storage conditions before analysis: ambient temperature - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: For the preparation of the stock solution (100 mg/L) the test substance was stirred for about 10 min. at 22 ± 10 °C in M4-Medium.
The nominal concentration of the stock solution was 100 mg/L. The test solutions were prepared by dilution the stock solution. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: STRAUS
- Source: Institut National de Recherche Chimique Appliqué
- Age at study initiation (mean and range, SD):
- Weight at study initiation (mean and range, SD):
- Length at study initiation (length definition, mean, range and SD):
- Valve height at study initiation, for shell deposition study (mean and range, SD):
- Peripheral shell growth removed prior to test initiation:
- Method of breeding:
- Feeding during test: none
ACCLIMATION
- Acclimation period:
- Acclimation conditions (same as test or not):
- Type and amount of food:
- Feeding frequency:
- Health during acclimation (any mortality observed):
QUARANTINE (wild caught)
- Duration:
- Health/mortality: - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 2,20 - 3,20 mmol/L
- Test temperature:
- 20 +/- 1 °C
- pH:
- 8.0 - 8.8
- Dissolved oxygen:
- 7.9 - 8.3 mg/L
- Nominal and measured concentrations:
- Nominal test concentrations (mg/L): 6.25, 12.5, 25, 50, 100, control
Analytically determined concentrations (mg/l):
at test start:
6.5, 24.2, 97.5 (104 % of nominal)
at test termination:
6.4, 24.15, 97.7 (102.4 % of nominal ) - Details on test conditions:
- TEST SYSTEM
- Test vessel: Test tubes (glass) with fiat bottom (20 mL)
- Fill volume: 10 mL
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
- Biomass loading rate: 0.5 animals /l test water
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: according to guideline
- Culture medium different from test medium: no
- pH: 8.0
- Total hardness: 2.20-3.20 mmol/L
- Alkalinity: 0.80-1.00 mmol/L (up to pH 4.3)
- Ca/mg ratio: ca. 4:1
- Conductivity: 550-650 µS/cm
OTHER TEST CONDITIONS
- Photoperiod: day night rhythm = 16 : 8 hours
- Light intensity: Artificial light, OSRAM L58 W31 warm white; About 5 -6 pE/(m2.S) in the range of 400 - 700 nm
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Swimming ability of the test animals (Visually, after 0, 3, 6, 24 and 48 h)
- Measurements: Temperature after 0, 24 and 48 h in an extra vessel close to the test vessels, pH and oxygen content after 0 and 48 h in one parallel at each concentration
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2
- Justification for using less concentrations than requested by guideline: not applicable
- Range finding study
- Test concentrations: no data
- Results used to determine the conditions for the definitive study: no data - Duration:
- 48 h
- Dose descriptor:
- EC0
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- act. ingr.
- Basis for effect:
- mobility
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Duration:
- 48 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Reported statistics and error estimates:
- Due to the results of the test a statistical evaluation of the data was unnecessary.
- Validity criteria fulfilled:
- yes
- Conclusions:
- The reported EC50 value at 48 hours was above 100 mg/L. The result is expressed as the nominal concentration.
Reference
Since the analytically determined concentrations were within +/-20% of the nominal concentrations, the results can be based on nominal concentrations.
Nominal conc. (mg/l) |
Cumulative immobility |
|||
3 h |
6 h |
24 h |
48 h |
|
Control |
0 |
0 |
0 |
0 |
6.25 |
0 |
0 |
0 |
0 |
12.5 |
0 |
0 |
0 |
0 |
25 |
0 |
0 |
0 |
0 |
50 |
0 |
0 |
0 |
0 |
100 |
0 |
0 |
0 |
0 |
Nominal conc. (mg/l) |
pH value |
Oxygen content (mg/L) |
||
0 h |
48 h |
0 h |
48 h |
|
Control |
8.0 |
8.0 |
8.2 |
8.1 |
6.25 |
8.1 |
8.1 |
8.3 |
8.1 |
12.5 |
8.2 |
8.1 |
8.2 |
8.1 |
25 |
8.3 |
8.1 |
8.2 |
7.9 |
50 |
8.6 |
8.2 |
8.3 |
8.0 |
100 |
8.8 |
8.4 |
8.3 |
8.1 |
In the control immobilization was < 10%. Thus, the validity criteria were fulfilled by the test.
Description of key information
The key value for acute toxicity to invertebrates was obtained from a study exposing Daphnia magna during 48 hours under GLP conditions and according to EEC Directive 79/831/EEC, Annex V, Part C. The 48-h EC50 for the test substance was > 100 mg/L. As a worst-case, a value of 48-h EC50 = 100 mg/L was used for the PNEC derivation.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Dose descriptor:
- EC50
- Effect concentration:
- 100 mg/L
Additional information
The acute toxicity of the test substance to the water flea Daphnia magna STRAUS was investigated in a 48-hour static test (BASF, 1998) according to EEC Directive 79/831/EEC, Annex V, Part C. Daphnia magna were exposed to different concentrations of test substance during 48 hours. Instead of mortality the test criterium of the acute toxicity is immobilization of the daphnids after 48 hours. Since the analytically determined concentrations were within +/- 20% of the nominal concentrations, the results were based on nominal concentrations. The results showed an 48-h EC50 of > 100 mg/L. In the control treatment immobilization was <= 10%. Thus, the validity criterium for the control treatment was fulfilled in the test.
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