Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Body responsible for the test

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method C.2 (Acute Toxicity for Daphnia)
Deviations:
not specified
GLP compliance:
yes

Test material

Constituent 1
Reference substance name:
Body responsible for the test
IUPAC Name:
Body responsible for the test

Sampling and analysis

Analytical monitoring:
not specified

Test solutions

Vehicle:
yes
Details on test solutions:
Identity and concentration of auxiliary solvent for dispersal: 1 g of the substance was dissolved in and made up to 10 mL with DMF. This solution was diluited to a concentration of 100 mg/l with water containing 2.3 mg/l Alkylphenol-polyglycolether

Test organisms

Test organisms (species):
other aquatic crustacea: DM

Study design

Test type:
not specified
Water media type:
not specified
Limit test:
no
Total exposure duration:
24 h

Test conditions

Hardness:
240 mg CaCO3/L

Results and discussion

Effect concentrationsopen allclose all
Duration:
24 h
Dose descriptor:
EC100
Effect conc.:
> 5.5 mg/L
Duration:
24 h
Dose descriptor:
EC0
Effect conc.:
< 0.5 mg/L

Any other information on results incl. tables

The immobility of most daphnias was affected by deposits of the test substance on their body. Therefore EC50 could not be determinated.

Applicant's summary and conclusion

Validity criteria fulfilled:
not specified
Conclusions:
EC0 < 0.5 mg/L (24h)
EC100 > 5.5 mg/L (24h)