Registration Dossier

Administrative data

Endpoint:
toxicity to microorganisms
Adequacy of study:
other information

Data source

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

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other: OECD Guideline No. 209 EC Directive 92/69/EEC Annex V Test Method C.11
GLP compliance:
yes

Study design

Test type:
other: aerobic
Total exposure duration:
3 h

Results and discussion

Effect concentrations
Duration:
3 h
Dose descriptor:
IC50
Effect conc.:
68.06 mg/L

Applicant's summary and conclusion