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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Description of key information

Under test conditions, the analogue URALAC ZW 3307 did not induce any visible effects on carp exposed to 0.40-0.46 mg/L (filtered solution) or 3.3 - 8.3 mg/L (unfiltered solution). The 96 h LC50 exceeds the water solubility limit of test substance and is considered to be >0.4 mg/L and the NOEC 0.4 mg/L, which corresponds to the measured concentration in the filtered solution. Since the registered substance and the substance URALAC ZW 3307 both contain the same main component and minor components with similar chemical structure, the 96 h LC50 for the registered substance exceeds the maximum soluble concentration of the test substance in test medium. See the full read-across report in section 13 for details.

Key value for chemical safety assessment

Additional information

In a 96 h acute toxicity study, carp (Cyprinus carpio) were exposed under static conditions to a single concentration of the analogue URALAC ZW 3307 at nominal concentrations of 0 (blank control) and 100 mg/L (measured concentrations: 0.40 -0.46 mg/L for filtered solution; 3.3 - 8.3 mg/L for unfiltered solution).Owing to the low solubility of Uralac ZW 3307 P in water (<0.9 mg/l), concentration levels toxic for carp could not be reached. The LC50 value is considered to be >0.4 mg/L and the NOEC 0.4 mg/L, which corresponds to the measured concentration in the filtered solution. The measured concentrations in the non-filtered solution are not used as this solution was turbid.The present toxicity study is classified as reliable without restrictions since it satisfies the requirements of the OECD Guideline No. 203.

Since the registered substance and the substance URALAC ZW 3307 both contain the same main component and minor components with similar chemical structure, the 96 h LC50 for the registered substance exceedthe maximum soluble concentration of the test substance in test medium.