Registration Dossier

Administrative data

Endpoint:
toxicity to microorganisms
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study has been presented to ECHA in the framework of a NONS notification. The document is now public because presented more than 12 years ago. The summary received is from migrated NONS dossier on analogue substance

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed
Year:
1988

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other: Directive 87/302/EEC L 133/118
GLP compliance:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent

Study design

Test type:
other: aerobic
Total exposure duration:
30 min

Results and discussion

Effect concentrationsopen allclose all
Duration:
30 min
Dose descriptor:
IC50
Effect conc.:
> 100 mg/L
Duration:
30 min
Dose descriptor:
NOEC
Effect conc.:
ca. 100 mg/L

Applicant's summary and conclusion