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Ecotoxicological information

Short-term toxicity to fish

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Study period:
28/02/2005 - 11/04/2005
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
T
Analytical monitoring:
no
Details on sampling:
- Concentrations: 100, 320, 560, 1000, 1800 mg/L
- Sampling method: Population mortality % measured over time.
Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Test material added by water accommodated fractions
- Controls: Negative control (0 mg/L test material)
Test organisms (species):
other: Scophthalmus maximus
Details on test organisms:
TEST ORGANISM
- Common name: Turbot
- Length at study initiation (length definition, mean, range and SD): 38.6 - 42.2 g
- Weight at study initiation (mean and range, SD): 1.671 - 2.272 g


ACCLIMATION
- Acclimation period: 12 days
- Acclimation conditions (same as test or not): No
- Type and amount of food during acclimation: pellet food form
- Feeding frequency during acclimation: at least twice a day
- Health during acclimation (any mortality observed): Mortality observations conducted daily
Test type:
semi-static
Water media type:
saltwater
Limit test:
yes
Total exposure duration:
96 h
Remarks on exposure duration:
Measurements taken at 0, 24, 48, 72 and 96 hours
Test temperature:
13.9-15.1 °C
pH:
6.67-8.11 over 96 hours
Dissolved oxygen:
99-103%
Conductivity:
51.4-55.0 mS/cm
Nominal and measured concentrations:
Nominal concentrations for test substance were 100, 320, 560, 1000, 1800 mg /L
Details on test conditions:
TEST SYSTEM
- Test vessel: soda-lime glass tank
- Material, size, headspace, fill volume: 14 L capacity
- Aeration: gentle aeration
- No. of organisms per vessel: 7
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Natural seawater from Scapa Flow, Orkney.
- Total organic carbon:
- Particulate matter: Sand filtered to 1 µM
- Alkalinity: pH 7.98
- Intervals of water quality measurement: Daily

OTHER TEST CONDITIONS
- Photoperiod: Constant illumination

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Mortality in test population

TEST CONCENTRATIONS
- Test concentrations: Nominal concentrations used were 100, 320, 560, 1000 and 1,800 mg/ L-1
Reference substance (positive control):
no
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
> 1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
> 1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
72 h
Dose descriptor:
LC50
Effect conc.:
> 1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Key result
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
other: LC90
Effect conc.:
1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
1 800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Details on results:
- Behavioural abnormalities:
- Mortality of control: Cumulative mortality (0.52%)
- Effect concentrations exceeding solubility of substance in test medium: Effect concentration exceeded maximum concentration tested.
Validity criteria fulfilled:
yes
Conclusions:
The study concludes that the LC50 for 24, 48, 72 and 96 hours was > 1800 mg/L, the LC90 for 96 hours was >1800 mg/L and the NOEC for 96 hours was > 1800 mg/L
Executive summary:

The study assessed the short-term toxicity of Monoethanolamine Salt of Nitrilotriacetic Acid to marine fish. The study was performed in compliance with GLP and in accordance with the testing guidelines OSPARCOM (1995): Protocol for a fish acute toxicity test. The test organisms used in this study was Scophthalmus maximus and all validity criteria were met. The results from the definitive test looked at 5 different concentrations of the test material (100, 320, 560, 1000 and 1800 mg/L) over 4 different time points (24, 48, 72 and 96 hours) with 1 replicate per concentration (7 organisms per replicate). The definitive test concentrations were derived from the allied Skeletonema toxicity test. Monoethanolamine Salt of Nitrilotriacetic Acid exhibited no effect at 1800 mg/L (direct addition) to the marine fish Scophthalmus maximus in the water phase after 96h.

Description of key information

The study assessed the short-term toxicity of Monoethanolamine Salt of Nitrilotriacetic Acid to marine fish. The study was performed in compliance with GLP and in accordance with the testing guidelines OSPARCOM (1995): Protocol for a fish acute toxicity test. The test organisms used in this study was Scophthalmus maximus and all validity criteria were met. The results from the definitive test looked at 5 different concentrations of the test material (100, 320, 560, 1000 and 1800 mg/L) over 4 different time points (24, 48, 72 and 96 hours) with 1 replicate per concentration (7 organisms per replicate). The definitive test concentrations were derived from the Skeletonema toxicity test. Monoethanolamine Salt of Nitrilotriacetic Acid exhibited no effect at 1800 mg/L (direct addition) to the marine fish Scophthalmus maximus in the water phase after 96h.

Key value for chemical safety assessment

Marine water fish

Marine water fish
Effect concentration:
1 800 mg/L

Additional information