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Diss Factsheets

Administrative data

Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Study test phase 2012-07-30 to 2012-08-03. Study report date 2012-08-31
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Meets the criteria as reliable without restriction according to Klimisch et al (1997).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2012
Report date:
2012

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 203 (Fish, Acute Toxicity Test)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
lithium 3-((3,4-dicyanophenyl)sulfonyl)propane-1-sulfonate)
EC Number:
700-777-2
Cas Number:
667889-11-4
Molecular formula:
C11H9N2O5S2Li
IUPAC Name:
lithium 3-((3,4-dicyanophenyl)sulfonyl)propane-1-sulfonate)
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
- Storage condition of test material: Ambient temperature

Sampling and analysis

Analytical monitoring:
yes
Details on sampling:
- Concentrations: 120 mg/L
- Sampling method: samples taken from the control and exposure test concentration at 0h and 96h

Test solutions

Vehicle:
yes
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION Required amount of test material was directly weighed into a glass vial and added to the dilution water in the test tank and stirred for 5 minutes.
- Evidence of undissolved material: Final solution clear and colourless

Test organisms

Test organisms (species):
Oncorhynchus mykiss (previous name: Salmo gairdneri)
Details on test organisms:
TEST ORGANISM
- Common name: Rainbow trout
- Source: Houghton Springs Fish Farm, Winterbourne Houghton, Blandford Forum, Dorset, DT11 0PD
- Feeding during test: None

ACCLIMATION
- Acclimation period: 40 days
- Acclimation conditions : same as test
- Type and amount of food: fed daily with commercial fish food
- Health during acclimation: 2 mortalities (<1%) recorded within 7 days prior to start of study

Study design

Test type:
not specified
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
96 h

Test conditions

Test temperature:
14.9 - 15.5 deg. C
pH:
7.15 - 7.79
Dissolved oxygen:
8.08 - 9.71 mg/L
Nominal and measured concentrations:
The measured concentration of test material at both the start and the end of the study was 124 mg/L. Based on the results of this analysis the nominal concentration was used for reporting the results.
Details on test conditions:
TEST SYSTEM
- Test vessel: Glass tanks
- Size: Test vessels with a working volume of 30L
- Aeration: Yes
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Tap water coarsely filtered to remove particulate material, passed through activated carbon and dechlorinated using sodium thiosulphate. Salts added to maintain hardness levels and the treated water passed through a UV steriliser and filtered to 10um. Dilution water was delivered to header tank and set to nominal test temp of 15 +/-1 deg. C
- Particulate matter: <3 mg/L (water supply)
- Chlorine: Total <2 ug/L (water supply)
- Alkalinity: 26.0 mg/L as CaCO3 (water supply)
- Conductivity: 189.5 uS/cm (water supply)

OTHER TEST CONDITIONS
- Photoperiod: 16h light & 8h dark with 20 min. transition period.

EFFECT PARAMETERS MEASURED: Observations of mortality and symptoms of toxicity were made at 3, 24, 48, 72 & 96h

TEST CONCENTRATIONS
- Test concentration: 120 mg/L
Reference substance (positive control):
no

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
> 120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
> 120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
72 h
Dose descriptor:
LC50
Effect conc.:
> 120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LOEC
Effect conc.:
> 120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality (fish)
Details on results:
- Behavioural abnormalities: none
- Observations on body length and weight: 49-60 mm and 1.54-2.71 g
- Mortality of control: 0
- Other adverse effects control: none
- Abnormal responses: none
- Any observations that might cause a difference between measured and nominal values: Solutions were clear and colourless

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
No mortalities were observed in the control or the 120 mg/L test concentration during this study. Therefore the 96h LC50 was determined to be >120 mg/L. It is concluded that 120 mg/L of the test substance did not have a significant toxic effect on the test organism, Oncorhynchus mykiss, in this study.
Executive summary:

Introduction

This study was performed to assess the acute toxicity of the test substance to rainbow trout Oncorhynchus mykiss. The method was designed to be compatible with:

OECD 203, Fish, Acute Toxicity Test. Adopted 17 July 1992.

Results & Conclusions

No mortalities were observed in the control or the 120 mg/L test concentration during this study. Therefore the 96h LC50 was determined to be >120 mg/L. It is concluded that 120 mg/L of the test substance did not have a significant toxic effect on the test organism, Oncorhynchus mykiss, in this study.