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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Ecotoxicological information

Short-term toxicity to aquatic invertebrates

Administrative data

Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2017.10.16~2017.12.18
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2017
Report date:
2017

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Lithium bis(fluorosulfonyl)imide
EC Number:
686-526-7
Cas Number:
171611-11-3
Molecular formula:
F2 H N O4 S2 . Li
IUPAC Name:
Lithium bis(fluorosulfonyl)imide
Test material form:
solid: bulk

Test solutions

Vehicle:
no
Details on test solutions:
1) Duration : 48 hours under a static system
2) Loading : 20 Daphnia aged less than 24 hours were divided into 4 groups of five animals each
3) Exposure condition
100mL of test solution was filled up to the 125mL of glass beaker. The photoperiod was 16 hours light :
8 hours darkness, and the temperature of test water was 20 +/- 2 celcious

Test organisms

Test organisms (species):
Daphnia magna

Study design

Test type:
static
Limit test:
yes
Total exposure duration:
48 h

Test conditions

Test temperature:
20.6 celcious
pH:
8.10
Dissolved oxygen:
8.08mg/L
Details on test conditions:
no abnormal behaviours were observed in any of the test daphnia exposed to control and treatment group
during the test
Reference substance (positive control):
no

Results and discussion

Effect concentrations
Key result
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
> 100 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
Observation time(24hr) : EC50 > 71.8 mg/L NOEC : 71.8 mg/L
Observation time(48hr) : EC50 > 71.8 mg/L NOEC : 71.8 mg/L