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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Valid without restriction

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2005
Report date:
2005

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
GLP compliance:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
Name of the test substance: 505-Oximether
Purity: 84.7 % w/w

Sampling and analysis

Analytical monitoring:
yes

Test solutions

Vehicle:
yes
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test concentration was prepared by diluting an acetonic stock solution with dilution water.
The stock solution was prepared by weighing 0.0506 g test substance and diluting it in 100
mL acetone. This stock solution was further diluted with acetone to recieve stock solutions for
each test concentration (see scheme below). The required amount of the acetonic stock
solution was given into the test vessel. After evaporating of the acetone the test vesseis wer~
filled with test water. The test substance was dissolved in the test water using an ultra turraxl.*
lt was tried to maximize the recovery rates by a prolonged stirring period of 5 days before the
fish were inserted into the test solutions to reach the maximum solubility, since an increase in
the test concentrations was observed in another aquatic study over 3 days. However, in this
test no marked increase was observed during the 5 days stirring period and a decrease of
the concentrations was observed at the end of the exposure period.
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): acetone

Test organisms

Test organisms (species):
Danio rerio (previous name: Brachydanio rerio)
Details on test organisms:
- Test species: Zebrafish (Danio rerio)
- Animal suppier: Zierfisch-Center Klöckner, Ludwigshafen, Germany
- Body weight (wet weight): 0.30 g (0.24 - 0.42 g)
- Body length (from the top of the snout 3.3 cm (3.1 - 3.6 cm) to the end of the caudal fin):
- Age of the animals: Approx. 4 months

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
96 h

Test conditions

Details on test conditions:
- Dilution water source: Municipal water of the city of Frankenthal, not chlorinated and passed through a charcoal filter.
- Total hardness: about 1 mmol/l
Acid capacity: about 2.5 mmol/l
pH: 7.5 - 8.5
Ca content : about 40 mg/l
Mg content : about 5 mg/l
- Exposure vessel type: Test vessels: All glass aquaria (30 x 22 x 24 cm)
- Volume of water: 10 l
- Aeration: Continuous aeration with oil-free air, slight
- Photoperiod: 16 : 8 hours day-night regime
- One test vessel per treatment
- Number of animals per test concentration and control: 10
- pH during the test: 7.8 - 8.2
- Oxygen content during the test: 7.9 - 8.8 mg/l
- Water temperature: 22 - 23 °C;
- Duration of adaption: about 2 weeks Mortality during the adaption period: 0 %
- Withdrawal of food: 1 day before and during exposure.
Reference substance (positive control):
not specified

Results and discussion

Effect concentrationsopen allclose all
Duration:
96 h
Dose descriptor:
LC100
Effect conc.:
0.066 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
0.041 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC0
Effect conc.:
0.026 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mortality (fish)

Any other information on results incl. tables

Sublethal observations / clinical signs:
RS-Freetext:
Nominal concentrations (mg/l): 0.022, 0.05, 0.1, 0.22 and 0.5

An analytical dose-verification of the test item was carried out at day 1.

Nom. Conc. (mg/l) Mean Anal. Conc. (mg/l) % of Nom. Conc.
0 n.d. -
0.022 < loq -
0.05 0.0103 20.6
0.1 0.0188 18.8
0.22 0.0394 17.9
0.5 0.1047 20.9
(n.d. = not detectable, loq = limit of quantification)

LC 50 (48h): 0.041 mg/l
LC 50 (72h): 0.041 mg/l
LC 50 (96h): 0.041 mg/l


Biological observations:
St = stottering, D = swimming at the bottom, C = swimming at the surface, A = apathy

Table showing cumulative mortality:
Cumulative mortality

Nom. conc. (mg/l) 1h 4h 24h 48h 72h 96h
Control 0 0 0 0 0 0
0.022 0 0 0 0 0 0
0.05 0 0 0 0 0 0
0.1 0 0 0 0 0 0
0.22 0 0 0 0 0 0
0.5 0 3 8 10 10 10


Behavior of the test item during the test: No remarkable observations

Applicant's summary and conclusion

Validity criteria fulfilled:
yes