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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
other information
Study period:
from 16-NOV-2001 to 25-FEV-2002
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Test performed according to OECD 203 (with some deviation), but the validity criteria is not fulfilled (20% mortality in the control group)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
Deviations:
yes
Remarks:
no analytical monitoring, only 3 tested groups
Qualifier:
according to guideline
Guideline:
EU Method C.1 (Acute Toxicity for Fish)
Deviations:
yes
Remarks:
no analytical monitoring, only 3 tested groups
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
ADHBFA-Me
IUPAC Name:
ADHBFA-Me
Test material form:
other: liquid

Sampling and analysis

Analytical monitoring:
no

Test solutions

Vehicle:
no
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: the stock solution was prepared using 450.8 mg of test item mad up to 4500 mL of test medium, stirred during 4 hours

Test organisms

Test organisms (species):
Danio rerio (previous name: Brachydanio rerio)
Details on test organisms:
TEST ORGANISM
- Common name: Danio rerio
- Source: no data
- Length at study initiation (length definition, mean, range and SD): 3.28 cm (min: 2.9 cm, max: 3.5 cm)
- Feeding during test: no


ACCLIMATION
- Acclimation period: 7 days
- Acclimation conditions (same as test or not): no data
- Type and amount of food: no data
- Feeding frequency: no data
- Health during acclimation (any mortality observed): 0% mortality

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
96 h
Post exposure observation period:
none

Test conditions

Hardness:
90 mg of CaCO3 per litre of test medium
Test temperature:
21.0 °C to 23.1 °C
pH:
8.06 to 8.29
Dissolved oxygen:
98 to 105 mg/L
Nominal and measured concentrations:
0, 1, 10 and 100 mg/L (nominal)
Details on test conditions:
TEST SYSTEM
- Test vessel: tank of at least 4-litre capacity
- Type: supplied with cover
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): one
- No. of vessels per control (replicates): one
- Biomass loading rate: maximum 1 g/L

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: tap water
- Culture medium different from test medium: no data
- Intervals of water quality measurement: regularly (no other information)

OTHER TEST CONDITIONS
- Adjustment of pH: no
- Photoperiod: 12hr/12hr
- Light intensity: no data

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- mortality (at 2-4 hrs and then at 24, 48, 72 and 96 hrs)
- clinical observations (at 2-4 hrs and then at 24, 48, 72 and 96 hrs)

TEST CONCENTRATIONS
- Spacing factor for test concentrations: 10
- Justification for using less concentrations than requested by guideline: restricted test
Reference substance (positive control):
no

Results and discussion

Effect concentrations
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
10 - 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Details on results:
- Behavioural abnormalities: at 100 mg/L equilibrium problem, pigmentation problems and breating problems at 0-4 hrs. Nothing to report thereafter.
- Mortality of control: 1 death at 24 hrs and 2 death at 48 hours (20% mortality)
- Any observations (e.g. precipitation) that might cause a difference between measured and nominal values: none
- Effect concentrations exceeding solubility of substance in test medium: no data

Applicant's summary and conclusion

Validity criteria fulfilled:
no
Remarks:
20% mortality in control
Conclusions:
Danio rerio 96-hr LC50 is between 10 and 100 mg/L