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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicity to microorganisms

Currently viewing:

Administrative data

Link to relevant study record(s)

Description of key information

The validity criteria applied to this study type were met and therefore the study is considered valid.
The following endpoints are applied to this study data:
NOEC: 30.5 mg/L
LOEC: 97.7 mg/L
EC50: 347.2 mg/L

Key value for chemical safety assessment

EC50 for microorganisms:
347.2 mg/L
EC10 or NOEC for microorganisms:
30.5 mg/L

Additional information

The objective of this study was to determine the no observable effect concentration (NOEC) and the effect concentration for a 50% effect (EC50) for activated sludge exposed to the test substance. The study was undertaken according to OECD Guideline 209, Adopted July, 2010.

A range-finding test, was undertaken in order to establish suitable dose levels for the definitive test.

The definitive test rate concentrations were 9.5, 30.5, 97.7, 312.5 and 1000 mg/L and were achieved by direct addition of the test substance to the test vessels.

The activated sludge inoculum was collected from the sludge return line at Burley Menston Sewage Treatment Works (West Yorkshire, U.K.) which has a predominantly domestic catchment. The point of collection was to ensure that the activated sludge sample was relatively free of exogenous material.

For the definitive test the suspended solids concentration for the sludge was 3.244 g/L and was within the required range of 3 g/L ± 0.3 g/L. The pH of the sludge was adjusted to pH 7.3 by the addition of 2M NaOH.

The following endpoints are applied to this study data:

NOEC: 30.5 mg/L

LOEC: 97.7 mg/L

EC50: 347.2 mg/L

The validity criteria applied to this study type were met and therefore the study is considered valid.