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EC number: 226-546-1 | CAS number: 5422-34-4
- 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
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 10 Aug -06 Sep 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
- Report date:
- 2016
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- Version / remarks:
- version April 2004
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- Department of Health -The Department of Health of the Government of the United Kingdom
Test material
- Reference substance name:
- N-2-hydroxyethyllactamide
- EC Number:
- 226-546-1
- EC Name:
- N-2-hydroxyethyllactamide
- Cas Number:
- 5422-34-4
- Molecular formula:
- C5H11NO3
- IUPAC Name:
- N-2-hydroxyethyllactamide
Constituent 1
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: control and 100 mg/L, from the bulk test preparation at 0 hours and from the pooled replicates at 48 hours
- Sampling method and storage: All samples were taken and stored frozen prior to analysis.
Test solutions
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: A nominal amount of test item (100 mg) was dissolved in test water and the volume adjusted to 1 liter to give the 100 mg/L test concentration. The prepared concentration was inverted several times to ensure adequate mixing and homogeneity.
- Controls: yes
Test organisms
- Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: water flea
- Source: in-house laboratory cultures
- Age of parental stock (mean and range, SD): 1st instar Daphnia magna
- Feeding during test: no
- Food type: mixture of algal suspension (Desmodesmus subspicatus) and Tetramin® flake food suspension
- Frequency: daily (for culture)
- Medium: Elendt M7 medium
METHOD FOR PREPARATION AND COLLECTION OF EARLY INSTARS OR OTHER LIFE STAGES: The test was carried out using 1st instar Daphnia magna. Gravid adults were isolated the day before test initiation, such that the young daphnids produced overnight were less than 24 hours old. These young were removed from the cultures and used for testing.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 48 h
Test conditions
- Hardness:
- 250 mg/L as CaCO3
- Test temperature:
- test start and test end: 22 °C
- pH:
- test start: 7.5 - 7.6
test end: 7.9 - Dissolved oxygen:
- test start: 8.6 - 8.7 mg O2/L
test end: 7.5 mg O2/L - Nominal and measured concentrations:
- nominal: control and 100 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel
- Material, size, headspace, fill volume: 150 mL glass beakers (covered)
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Reconstituted water (ISO medium)
- Culture medium different from test medium: yes: Elendt M7 medium for the stock culture and Iso medium for the test
- Intervals of water quality measurement: Water temperature was recorded daily throughout the test. Dissolved oxygen concentrations and pH were recorded at the start and termination of the test
OTHER TEST CONDITIONS
- Adjustment of pH: Elendt M7 Medium: 7.9 ± 0.3; Reconstituted Water – ISO Medium: 7.8 ± 0.2
- Photoperiod: 16 hours light and 8 hours darkness with 20 minute dawn and dusk transition periods
- Light intensity:between 200 and 1200 Lux
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Immobilization or adverse reactions were recorded at 24 and 48 hours after the start of exposure. The criterion of effect used was that daphnia were considered to be immobilized if they were unable to swim within 15 seconds after gentle agitation.
VEHICLE CONTROL PERFORMED: no
RANGE-FINDING STUDY
- Test concentrations: 0.10, 1.0, 10 and 100 mg/L.
- Results used to determine the conditions for the definitive study: the test concentrations of the definitive test were based on the results of the range -finding test - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
Results and discussion
Effect concentrationsopen allclose all
- 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:
- NOEC
- Effect conc.:
- 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Details on results:
- - Behavioural abnormalities: A sub-lethal effect of exposure was observed in the 100 mg/L test concentration. One Daphnia was trapped at the surface.
- Mortality of control: no
- Others: Biological results of the range-finding test, the analytical results of the definitive test and the analytical results are summarized in the tables 1-3 in section "Any other information on results incl. tables". - Results with reference substance (positive control):
- potassium dichromate
EC50 (48h): 0.64 mg/L - Reported statistics and error estimates:
- An estimate of the EC50 values was given by inspection of the immobilization data.
Any other information on results incl. tables
Table 1: Results of the range-finding test
Nominal Concentration (mg/L) |
Observations (Initial Population: 10 Per Replicate) |
|||
24 Hours |
48 Hours |
|||
Cumulative Immobilized Daphnia |
Observations |
Cumulative Immobilized Daphnia |
Observations |
|
Control |
0 |
10 N |
0 |
10 N |
0.10 |
0 |
10 N |
0 |
10 N |
1.0 |
0 |
10 N |
0 |
10 N |
10 |
0 |
1 T 9 N |
0 |
1 T 9 N |
100 |
0 |
1 T 9 N |
0 |
10 N |
N = No sub-lethal effects observed
T = Trapped at surface
Validity criteria:
The test was considered as valid since:
No more than 10% of the control daphnids show immobilization or other signs of disease or stress.
The dissolved oxygen concentration at the end of the test is equal to or greater than 3 mg/L in the control and test vessels.
Table 2: Results of the definitive test after 24 h
Nominal Concentration (mg/L) |
24 Hours |
|||||||||
Cumulative Immobilized Daphnia (Initial Population: 5 Per Replicate) |
Observations |
|||||||||
R1 |
R2 |
R3 |
R4 |
Total |
% |
R1 |
R2 |
R3 |
R4 |
|
Control |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
100 |
0 |
0 |
0 |
1* |
1 |
5 |
5 N |
1 T 4 N |
5 N |
4 N |
R1 – R4 = Replicates 1 to 4
N = No sub-lethal effects observed
T = Trapping at the surface
*Single immobilized daphnid considered to be due to natural causes given that less than 10% immobilization was observed.
Table 2: Results of the definitive test after 48 h
Nominal Concentration (mg/L) |
24 Hours |
|||||||||
Cumulative Immobilized Daphnia (Initial Population: 5 Per Replicate) |
Observations |
|||||||||
R1 |
R2 |
R3 |
R4 |
Total |
% |
R1 |
R2 |
R3 |
R4 |
|
Control |
0 |
0 |
0 |
0 |
0 |
0 |
5 N |
5 N |
5 N |
5 N |
100 |
0 |
0 |
0 |
1* |
1 |
5 |
5 N |
1 T 4 N |
5 N |
4 N |
R1 – R4 = Replicates 1 to 4
N = No sub-lethal effects observed
T = Trapping at the surface
*Single immobilized daphnid considered to be due to natural causes given that less than 10% immobilization was observed.
Table 3: Analytical results
Time Point |
Nominal Concentration of Test Item in Test Sample |
Sample Preparation Factor |
Determined Concentration of Test Item in Test Sample |
Percentage of Nominal Concentration |
cnom |
F |
c |
||
[hours] |
[mg/L] |
|
[mg/L] |
[%] |
0 |
Control |
1 |
<LOQ |
- |
100 |
100 |
115 |
115 |
|
48 |
Control |
1 |
<LOQ |
- |
100 |
100 |
114 |
114 |
LOQ = Limit of Quantification
- = not applicable
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
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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