Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
short-term toxicity to aquatic invertebrates
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Deviations:
yes
Remarks:
Limited number of animals per concentration; low hardness
GLP compliance:
no
Specific details on test material used for the study:
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- Treatment of test material prior to testing: test compound dissolved in acetone
Analytical monitoring:
not specified
Details on sampling:
- Concentrations: 0.24 mg/L; 0.16 mg/L; 0.10 mg/L; 0.065 mg/L; 0.042 mg/L; 0.028 mg/L; 0.018 mg/L; 0.012 mg/L.
Vehicle:
yes
Remarks:
acetone
Details on test solutions:
PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: For each test concentration, the appropriate amount of test compound, dissolved in acetone, was pipetted into 500 ml of diluent water and mixed with a magnetic stirrer. The remaining 50 ml were used for 0-hour pH and DO determinations.
- Controls: Negative controls (same dilution water and conditions but with no test substance or acetone) and positive controls (containing greatest amount of acetone introduced into any one test vessel).
- Chemical name of vehicle (organic solvent, emulsifier or dispersant): Acetone
Test organisms (species):
Daphnia magna
Details on test organisms:
TEST ORGANISM
- Common name: Water flea
- Source: Laboratory stocks cultured at Bionomics
- Age of parental stock: <= 24 hours
Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
48 h
Hardness:
35 mg/L CaCO3
Test temperature:
21 ± 1 °C
pH:
7.1
Dissolved oxygen:
> 60% saturation
Nominal and measured concentrations:
Nominal concentrations (mg/L): 0.24; 0.16, 0.10; 0.065; 0.042; 0.028; 0.018; 0.012.
Details on test conditions:
TEST SYSTEM
- Test vessel: 250 ml beaker
- Material, size, headspace, fill volume: 250 ml beaker containing 150 ml test solution
- Aeration: Test solutions were not aerated during the tests
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 3

TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Well water was used to culture the water fleas. Prior to the test, diluent water was filtered through polyester fiber and sterilized with an ultraviolet light to remove any microorganisms.
- Intervals of water quality measurement: Dissolved oxygen concentration, pH and temperature of test solutions were checked at 0 and 48 hours in the highest, middle and lowest test concentrations, at a minimum.

EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : percentage mortality at 24 and 48 hours

VEHICLE CONTROL PERFORMED: yes

RANGE-FINDING STUDY
- Test concentrations: The preliminary test defined a narrower range of concentrations to be used in the definitive test which would then assess the dose-response relationship and permit calculation of an LC50 and its 95% confidence interval from the mortality data produced.
Reference substance (positive control):
no
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
0.13 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Key result
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
0.039 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
0.018 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
mortality
Details on results:
- Other biological observations: All dead water flea observed during this exposure were carrying a partially attached carapace, suggesting the organisms died while attempting to moult.
- Mortality of control: No mortality
- Other adverse effects control: No effects
Reported statistics and error estimates:
LC50 (24hr) = 0.068 - 0.26 mg/L (95% confidence interval)
LC50 (48hr) = 0.030 - 0.052 mg/L (95% confidence interval)

Table showing concentrations tested and corresponding average observed percentage mortalities for the water flea (Daphnia magna) exposed to hexachlorocyclopentadiene:

 Nominal concentration (mg/L)     Average percentage mortality   
 24 hr  48 hr
 0.24 87   100
 0.16  33  100
 0.10  33  100
 0.065  40  93
 0.042  7  57
 0.028  0  20
 0.018  0  0
 0.012  0  0
control (acetone)   0  0
 control  0  0
Validity criteria fulfilled:
yes
Conclusions:
The 48 hr LC50 of hexachlorocyclopentadiene for Daphnia magna was 0.039 mg/L.
Executive summary:

The short-term toxicity of hexachlorocyclopentadiene to the freshwater invertebrate species Daphnia magna was determined using a procedure equivalent to the OECD Guideline for Testing of Chemicals 202, with acceptable restrictions. The study determined the average percent mortality over a range of concentrations between 0.012 - 0.24 mg/L. It was determined that the 48 hr LC50 of the registered substance was 0.039 mg/L.

Description of key information

Two non-GLP short-term toxicity studies were performed according to a method similar to the OECD Testing Guideline 202 on Daphnia magna. The lowest 48-hour EC50 was 0.039 mg/l. It was selected as the key value as it represents a worst-case scenario.

Key value for chemical safety assessment

Fresh water invertebrates

Fresh water invertebrates
Effect concentration:
0.039 mg/L

Additional information

The short-term toxicity of the registered substance to marine invertebrates was not investigated as part of this REACH Registration. It was not considered as relevant taking into account the uses of the substance.