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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP Guideline study, test was performed with sludge from municipal waste water treatment plant

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1995
Report date:
1995

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
Reference substance name:
6-methylhept-5-en-2-one
EC Number:
203-816-7
EC Name:
6-methylhept-5-en-2-one
Cas Number:
110-93-0
IUPAC Name:
6-methylhept-5-en-2-one
Details on test material:
- Name of test material (as cited in study report): 2-methylhepten-2-on-6
- Lot/batch No.: 94-1739
- Analytical purity: > 98 %
- Impurities (identity and concentrations): 2-methyl-2-hepten-6-ol: < 1%

Sampling and analysis

Analytical monitoring:
no

Test organisms

Test organisms (species):
activated sludge, domestic
Details on inoculum:
Test mixture contained test substance (1g/l), sewage feed (as prescribed by OECD 209) and activated sludge from laboratory wastewater treatment plants treating municipal wastewater.

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
30 min

Test conditions

Nominal and measured concentrations:
- Test concentrations (mg/L): 20, 100, 250, 500, 1000 (nominal)
Details on test conditions:
TEST CONDITIONS
Test mixture (total volume 250 ml) was incubated at 20+/-2°C for 30 minutes, after which the respiration rate was measured.

TEST SYSTEM
The following controls were included:
- Inoculum blank: control without test substance but with inoculum (3 flasks)
- Positive control: with inoculum (3 flasks, 1, 10, and 100 mg/l).
Reference substance (positive control):
yes
Remarks:
3,5-dichlorophenol

Results and discussion

Effect concentrationsopen allclose all
Duration:
30 min
Dose descriptor:
other: EC20
Effect conc.:
ca. 27 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Duration:
30 min
Dose descriptor:
EC50
Effect conc.:
800 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Details on results:
Respiration rate
Test substance Inhibition (mgO2/l*h) Inhibition (%)
20 mg/l 13 -19
100 mg/l 12 -25
250 mg/l 11 -31
500 mg/l 10 -38
1000 mg/l 7 -56
Results with reference substance (positive control):
Respiration rate
Reference substance Inhibition (mgO2/l*h) Inhibition (%)
1 mg/l 15 -6
10 mg/l 9 -44
100 mg/l 1 -94

The EC20 for the reference 3,5-dichlorophenyl was 2.5 mg/l and the EC50 was 15 mg/l. The EC50 for the reference is valid because of ranging between 5 and 30 mg/l as validity criteria.

Applicant's summary and conclusion