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EC number: 253-668-2 | CAS number: 37788-55-9
- 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:
- 11. Dec. 2018 - 20. Dec. 2018
- 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)
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Vehicle:
- no
- Details on test solutions:
- Nominal concentrations [mg/L]: 0 (blank control), 4.6, 10, 22, 46, 100
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- Species Daphnia magna
Authority STRAUS
Strain Berlin
Sex female
Age between 0 and 24 hours
Origin Umweltbundesamt Berlin - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- Resulting hardness in mmol/L: 2.502
Resulting hardness in mg CaCO3/L: 250 - Test temperature:
- 19.6 - 23.3 °C
- pH:
- 7.8 - 8.2
- Dissolved oxygen:
- 8.5 - 9.3 mg/L
- Details on test conditions:
- Medium renewal: twice a week
Photo period: 16/8 hours, using neon tubes - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Key result
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- LOEC
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 100 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality
- Validity criteria fulfilled:
- yes
- Conclusions:
- Based on the test results the EC50, 48h for Daphnie magna can be stated to be > 100 mg/L.
- Executive summary:
Two valid experiments were performed.
The 1stexperiment was performed using one concentration of 100 mg/L (limit test). For the test concentration and the blank control, 20 Daphnia were exposed to the test item for 48 hours in a static test system. After 24 and 48 hours, the immobilised Daphnia were counted.
In this experiment more than 10 % of the Daphnia in the test concentration were immobilised and therefore a 2ndexperiment was performed using 5 concentrations ranging from 4.6 to 100 mg/L (full test). The test was carried out under the same conditions like the 1stexperiment.
The biological results base on the results of the second experiment.
The two lowest concentrations (4.6 mg/L and 10 mg/L) were excluded from the evaluation of the biological results, because they showed no significant toxicity compared to the control.
The two highest concentrations (46 mg/L and 100 mg/L) showed toxicity between 5 and 15 % immobilisation. None of the animals was immobilised in the blank control.
At the beginning and at the end of the test, the content of the test item in the test solutions was determined usingHPLC-UV-determination. The measured concentrations in the 3 highest concentrations were between 98 % and 104 % of the nominal concentration at the beginning and between 108 % and 115 % of the nominal concentrations at the end of the test. Therefore, the determination of the biological results was based on the nominal concentrations of the second experiment.
Potassium dichromate K2Cr2O7(CAS No. 7778-50-9) was used as positive controlin a current reference study to assure that the test conditions are reliable.
The following results were determined for the test itemN-(2-hydroxypropyl)imidazole, purified by distillation(species:Daphnia magna).48h-NOEC≥100 mg/L
48h-LOEC> 100mg/L
48h-EC50> 100 mg/LThe immobilisation of 15 % at the concentration of 100 mg/L lay in the same range as in the limit test (20 %), but the evaluation program does not recognize this as a significant difference in comparison to the control. Therefore, the NOEC was determined as≥the highest tested concentration.
Reference
Immobility
1stExperiment
In the blank control, one of the Daphnia was immobilised (see table below).
Table7.1‑a Immobility
Nominal Concentration in mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
absolute |
in % |
absolute |
in % |
|||||||
Blank control |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
0 |
0 |
5 |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
1 |
20 |
2ndExperiment
In the blank control, none of the Daphnia was immobilised (see table below).
Table7.1‑b Immobility
Nominal Concentration in mg/L |
Immobility 24 hours |
Immobility 48 hours |
||||||||
absolute |
in % |
absolute |
in % |
|||||||
Blank control |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
4.6 * |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
5 |
10 * |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
22 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
46 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
5 |
100 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
1 |
2 |
15 |
* The two lowest concentrations (4.6 mg/L and 10 mg/L) were excluded from the evaluation of the biological results, because they showed no significant toxicity compared to the control.
Description of key information
A study according to OECD 202 was conducted.
Based on the test results the EC50, 48h for Daphnie magna can be stated to be > 100 mg/L.
Thus the test material is not toxic towards aquatic invertebrates according to the criteria of CPL.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 100 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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