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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
4-chloro-3,5-dinitro-α,α,α-trifluorotoluene
EC Number:
206-889-3
EC Name:
4-chloro-3,5-dinitro-α,α,α-trifluorotoluene
Cas Number:
393-75-9
Molecular formula:
C7H2ClF3N2O4
IUPAC Name:
4-chloro-3,5-dinitro-α,α,α-trifluorotoluene

Test organisms

Test organisms (species):
Daphnia magna

Study design

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

Test conditions

Hardness:
250 mg/l
Test temperature:
20-21°C
pH:
8.0-8.1
Nominal and measured concentrations:
Due to the low water solubility a supersaturated stock suspension of the test item with a nominal concentration of 100 mg/l was continuously stirred at room temperature in the dark over 96 hours and filtered. The dilutions 1:100, 1:222, 1:454, 1:1000 and 1:2222 of the filtrate were used as test media.
The mean analytically determined test item concentration in the analyzed test media samples (dilutions 1:454, 1:222 and 1:100) amounted to 0.18, 0.38 and 0.88 mg/l at the start of the test. The values found at the end of the test ranged from 98-106% of the initially measured values.
The lowest test concentrations (dilutions 1:1000 and 1:2222) were not analysed since below the 48-hr NOEC.

Results and discussion

Effect concentrationsopen allclose all
Duration:
48 h
Dose descriptor:
EC50
Effect conc.:
0.6 mg/L
Nominal / measured:
meas. (geom. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Remarks on result:
other: 0.5-0.7 mg/l
Duration:
48 h
Dose descriptor:
NOEC
Effect conc.:
0.38 mg/L
Nominal / measured:
meas. (geom. mean)
Conc. based on:
test mat.
Basis for effect:
mobility
Duration:
48 h
Dose descriptor:
EC100
Effect conc.:
1.9 mg/L
Nominal / measured:
estimated
Details on results:
All biological test results are related to the total mean measured test item concentrations of 0.19 mg/l (1:454), 0.38 mg/l (1:222) and 0.87 mg/l (1:100), calculated as the average over all measurements per test concentration during the test period.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes