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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
short-term toxicity to fish
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1997

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method C.1 (Acute Toxicity for Fish)
Version / remarks:
OECD 203
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
424-210-0
EC Name:
-
Cas Number:
23911-85-5
Molecular formula:
C29 H24 O7
IUPAC Name:
2-benzoyl-5-[3-(4-benzoyl-3-hydroxyphenoxy)-2-hydroxypropoxy]phenol

Test solutions

Details on test solutions:
Identity and concentration of auxiliary solvent for dispersal: Dimethylformamide in dechlorinated tap water.

Test organisms

Test organisms (species):
Oncorhynchus mykiss (previous name: Salmo gairdneri)

Study design

Test type:
static
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
96 h

Test conditions

Hardness:
Total hardness was approximately 100 mg/l as CaCO3
Test temperature:
The water temperature was controlled at 14°C
Dissolved oxygen:
greater than or equal to 9.2 mg O2/l
Nominal and measured concentrations:
The test concentrations to be used in the definitive study were determined by preliminary range-finding studies.
An initial range finding study was performed whereby fish were exposed to a series of concentrations of 0.020 and 0.20 mg/l under static test conditions. A second range finding study was performed to concentration 0.10 mg/l.
There were no sub-lethal effects of exposure during the range-finding study. The results of the range-finding studies showed no mortalities at the test concentrations of 0.020, 0.1 and 0.20 mg/l. However, precipitation of the test material was observed at 0.20 mg/l indicating 0.10 mg/l to be the maximum limit of water solubility of the test material under these test conditions.
Based on this information, a single test concentration, in duplicate, of 0.10 mg/l was selected for the definitive study. This experimental design conforms to a "Limit test', to confirm that at the highest attainable test concentration of 0.10 mg/l, no mortalities or sub-lethal effects of exposure were observed.

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
LC50
Effect conc.:
> 0.1 mg/L
Basis for effect:
mortality (fish)
Duration:
48 h
Dose descriptor:
LC50
Effect conc.:
> 0.1 mg/L
Basis for effect:
mortality (fish)
Duration:
72 h
Dose descriptor:
LC50
Effect conc.:
> 0.1 mg/L
Basis for effect:
mortality (fish)
Key result
Duration:
96 h
Dose descriptor:
LC50
Effect conc.:
> 0.1 mg/L
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
LC100
Effect conc.:
> 0.1 mg/L
Basis for effect:
mortality (fish)
Duration:
96 h
Dose descriptor:
NOEC
Effect conc.:
>= 0.1 mg/L

Any other information on results incl. tables

Sublethal observations / clinical signs:

There were no sub-lethal effects observed in 20 fish exposed to a test concentration of 0.10 mg/l for a period of 96 hours.

Applicant's summary and conclusion

Conclusions:
The acute toxicity of Fadex He 1819 PK to the freshwater fish rainbow trout (Oncorhynchus mykiss) has been investigated and gave a 96-Hour LC50 of greater than 0.10 mg/|. Correspondingly the No Observed Effect Concentration was greater than or equal to 0.10 mg/l.