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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987
Report date:
1987

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: German Industrial Standard DIN 38412 part 15
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
sodium carboxylate solution
IUPAC Name:
sodium carboxylate solution
Details on test material:
- name: Sodium carboxylate solution
- purity: not specified

Sampling and analysis

Analytical monitoring:
no

Test solutions

Vehicle:
not specified

Test organisms

Test organisms (species):
Leuciscus idus
Details on test organisms:
- Test fish: Leuciscus idus (golden variety)
- Supplier: Fischzucht Paul Eggers, 2354 Hohenweststedt, Germany
- Body length: 5.8 cm (range 5.1 - 6.4 cm)
- Body weight: 2.4 g (range 1.8 - 3.3 g)
- Loading rate (g fish/l test water): 2.4
- Medical treatment: twice with 0.05 mg/l malachite green chloride, once with 10 mg/l tetracycline hydrochloride

Study design

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

Test conditions

Test temperature:
20 - 21 °C
pH:
7.6 - 10.0
Dissolved oxygen:
7.5 - 8.7 mg/l
Details on test conditions:
- Dilution water source: reconstituted freshwater according to DIN 38412, Part II, 1982

Dilution water chemistry
- Total hardness: 2.5 mmol/l
- Acid capacity: 0.8 mmol/l
- Ratio Ca/Mg ions: 4:1
- Ratio Na/K ions: 10:1
- pH: about 7.7
- The test solution was prepared by adding the test item to the test media without any pre-treatment. Then, the fish were placed into the test aquaria. Nominal test concentrations: 5000 and 10000 mg/l. In addition, a control was tested in parallel.
- Test vessels: All glass aquaria (30 x 22 x 24 cm)
- Volume of water: 10 l
- Continuous aeration with oil-free air, slight
- Photoperiod: 16 : 8 hours day-night regime
- One test vessel per treatment
- No of animals per test concentration and control: 10
- Duration of adaption: about 2 weeks
- Mortality during the adaption period: 0 %
- Withdrawal of food: 1 day before and during exposure.
- observations: mortality and symptoms after 0, 4, 24, 48, 72, and 96 h
- measurements: pH and oxygen content after 0, 24, 48, 72 and 96 h
- Statistical methods: The median lethal concentration (LC50) was calculated using Probit Analysis (Finney D.J., Probit Analysis, Cambr. Univ. Press, 3rd Edition, 1971)

Results and discussion

Effect concentrationsopen allclose all
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 10 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC100
Effect conc.:
> 10 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
10 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC0
Effect conc.:
10 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)

Any other information on results incl. tables

Sublethal observations / clinical signs:
RS-Freetext:
No analytical dose-verification of the test item was carried out.

LC 50 (48h): > 10000 mg/l
LC 50 (72h): > 10000 mg/l
LC 50 (96h): > 10000 mg/l

Table showing cumulative mortality:
Cumulative mortality

Nom. conc. (mg/l) 1h 4h 24h 48h 72h 96h
Control 0 0 0 0 0 0
5000 0 0 0 0 0 0
10000 0 0 0 0 0 0

No symptoms observed

Reference substances (if used):
48 h-LC50 of the positive control Chloroacetamide: about 32 mg/l (corresponds to normal sensitivity).


Behavior of the test item during the test:

No remarkable observations.

Applicant's summary and conclusion