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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1998
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Reliability rating was 1 because study was carried out using OECD 209 test guideline and was performed under GLP.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
GLP compliance:
yes

Test material

Constituent 1
Constituent 2
Reference substance name:
MCP 1440
IUPAC Name:
MCP 1440
Details on test material:
- Name of test material (as cited in study report): MCP 1440
- Physical state: Liquid
- Analytical purity: 100%

Sampling and analysis

Analytical monitoring:
no

Test solutions

Vehicle:
no

Test organisms

Test organisms (species):
activated sludge of a predominantly domestic sewage
Details on inoculum:
Activated sludge was collected from municipal wastewater treatment plant that handles predominantly domestic waste.
Suspended solids in the collected activated sludge sample was determined. The collected activated sludge was diluted as need to provide 8 liters of activated sludge inoculum with a nominal suspended solid conc of 4 gm/L. pH of the activated sludge was maintained between pH 6-8. Inoculum was not acclimated or adapted to the test substance before start of study.

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h

Test conditions

pH:
pH 6-8
Nominal and measured concentrations:
Test material evaluated at 1, 10, 100 and 1000 mg/L nominal concentration.
Positive control, 3,5-DCP was evaluated at 5, 15 and 45 mg/L concentrations.
Reference substance (positive control):
yes
Remarks:
3,5-DCP

Results and discussion

Effect concentrationsopen allclose all
Duration:
3 h
Dose descriptor:
other: EL50
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Remarks:
nominal loading
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Duration:
3 h
Dose descriptor:
other: NOEL
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Remarks:
nominal loading
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Results with reference substance (positive control):
In order for the test to be valid, ghd OECD 209 guidelines require that the EC50 for positive control (3,5-DCP) be in the range of 5 to 30 mg/L. In this test, 3,5-DCP was found to have an EC50 of 6 mg/L which satisfies the guideline requirement.

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
The test substance did not inhibit the respiration of activated sludge microorganisms. The 3 hr EL50 value was determined to be >1000 mg/L . The 3 hr NOEL was estimated to be >1000 mg/L. Overall, these results indicate that the test substance was not toxic to aquatic microorganism or bacteria in activated sludge inoculum.
Executive summary:

The test substance did not inhibit the respiration of activated sludge microorganisms. The 3 hr EL50 value was determined to be >1000 mg/L (nominal). The 3 hr NOEL was estimated to be >1000 mg/L (nominal). Overall, these results indicate that the test substance was not toxic to aquatic microorganism or bacteria in activated sludge inoculum.