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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1990-08-2 to 1990-09-03
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: According OECD 209, non GLP, limited information on test substance. Justification for read-across see chemical safety report chapter 1.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1990
Report date:
1990

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
Deviations:
yes
Principles of method if other than guideline:
Instead of using 3,5-dichlorophenol as reference (acc. to OECD 209) potassium dichromate was used in a concentration to inhibit respiration of 50%.
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Quaternary ammonium compounds, C20-22-alkyltrimethyl, chlorides
EC Number:
271-756-9
EC Name:
Quaternary ammonium compounds, C20-22-alkyltrimethyl, chlorides
Cas Number:
68607-24-9
IUPAC Name:
68607-24-9
Constituent 2
Reference substance name:
C20/22 ATQ
IUPAC Name:
C20/22 ATQ
Specific details on test material used for the study:
Details on properties of test surrogate or analogue material (migrated information):
no furhter details are available

Sampling and analysis

Analytical monitoring:
no
Details on sampling:
not applicable as nominal test concentrations are evaluated

Test solutions

Vehicle:
no
Details on test solutions:
no further details available

Test organisms

Test organisms (species):
activated sludge, domestic
Details on inoculum:
- Laboratory culture: activated sludge from municipal waste water treatment plant Hildesheim
- Method of cultivation:
- Preparation of inoculum for exposure: washed twice with dechlorinated, autoclaved tap water
- Pretreatment: none
- Initial biomass concentration: 1.251 g/L dry weight

Study design

Test type:
static
Water media type:
freshwater
Limit test:
no
Total exposure duration:
3 h
Post exposure observation period:
not applicable

Test conditions

Hardness:
not specified
Test temperature:
22°C
pH:
not specified
Dissolved oxygen:
not specified
Salinity:
not specified
Nominal and measured concentrations:
nominal: 10 - 18 - 32 - 58 - 100 - 180 mg/L
Details on test conditions:
TEST SYSTEM
TEST SYSTEM
- Test vessel:500 mL Erlenmeyer flasks
- Type (delete if not applicable): not specified
- Material, size, headspace, fill volume: 500mL
- Aeration: yes, permanently
- Type of flow-through (e.g. peristaltic or proportional diluter): not specified
- Renewal rate of test solution (frequency/flow rate):not specified
- No. of organisms per vessel:not specified
- No. of vessels per concentration (replicates):1
- No. of vessels per control (replicates):1


TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: synthetic water acc. to OECD 209

OTHER TEST CONDITIONS
- Adjustment of pH: not specified
- Photoperiod: not specified
- Light intensity: not specified



Reference substance (positive control):
yes
Remarks:
kaliumdichromat

Results and discussion

Effect concentrationsopen allclose all
Duration:
3 h
Dose descriptor:
EC10
Effect conc.:
9.5 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Remarks on result:
other: n.a.
Duration:
3 h
Dose descriptor:
other: EC20
Effect conc.:
16 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Remarks on result:
other: n.a.
Duration:
3 h
Dose descriptor:
EC50
Effect conc.:
43 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Remarks on result:
other: n.a.
Duration:
3 h
Dose descriptor:
other: EC80
Effect conc.:
120 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Remarks on result:
other: n.a.
Details on results:
no further details available
Results with reference substance (positive control):
- Results with reference substance valid? yes
- Relevant effect levels: 32 - 58 - 100 mg/ L
Reported statistics and error estimates:
no further details available

Any other information on results incl. tables

no further details available

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
Test results are plausible and valid:
EC 10-value: 9.5 mg/L
EC 20-value: 16 mg/L
EC 50-value: 43 mg/L
EC 80-value: 120 mg/L

P 95 %: 11.26 < 43 < 164.17
Executive summary:

Test results are plausible and valid. Level of detail in the report reflect testing strategy and reporting of 1990.