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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
toxicity to microorganisms
Type of information:
experimental study
Adequacy of study:
key study
Study period:
29th July - 4th August 1999
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: done under GLP and OECD method

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1999
Report date:
1999

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: EC Directive 88/302 'Biodegradation-Activated Sludge Respiration Inhibition test' and OECD guideline No.209'
GLP compliance:
yes

Test material

Study design

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

Results and discussion

Effect concentrationsopen allclose all
Duration:
3 h
Dose descriptor:
IC50
Effect conc.:
> 100 mg/L
Duration:
3 h
Dose descriptor:
NOEC
Effect conc.:
100 mg/L

Applicant's summary and conclusion

Conclusions:
BMS 217947-01 had no biologically significant inhibitory effect on the respiration rate of activated sludge at 100mg/l, the highest concentration tested. The EC20, EC50 and EC80 of the test substance could not, therefore, be calculated but these must be greater than 100mg/ml, the highest level tested.
Executive summary:

BMS 217947-01 had no biologically significant inhibitory effect on the respiration rate of activated sludge at 100mg/l, the highest concentration tested. The EC20, EC50 and EC80 of the test substance could not, therefore, be calculated but these must be greater than 100mg/ml, the highest level tested.