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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The test was conducted according to relevant guidelines.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1994
Report date:
1994

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
other: Directive 88/302/EEC
Qualifier:
according to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
[29H,31H-phthalocyaninetrisulphonyl trichloridato(2-)-N29,N30,N31,N32]copper
EC Number:
248-236-5
EC Name:
[29H,31H-phthalocyaninetrisulphonyl trichloridato(2-)-N29,N30,N31,N32]copper
Cas Number:
27121-30-8
Molecular formula:
C32H13Cl3CuN8O6S3
IUPAC Name:
Copper, [29H,31H-phthalocyanine-C,C,C-trisulfonyl trichloridato(2-)-kN29,kN30,kN31,kN32]-

Sampling and analysis

Analytical monitoring:
no

Test solutions

Details on test solutions:
A stock solution (nominal concentration 2000 mg/L) was prepared. 200 mg/L test were placed in a beaker in mixed with 800 mL water. After stirring for 1.5 hours at 19°C, the test solution was adjusted with diluted sodium hydroxide from pH 2.1 to 7.0 und filled up to 1 L.
Nominal concentrations of 250 mg/L, 500 mg/L and 1000 mg/L were tested.

Test organisms

Test organisms (species):
activated sludge, domestic
Details on inoculum:
Source: municipal sewage treatment works of Frankfurt/M-Sindlingen
Pretreatment: according to the guideline
Acclimatization: Not pre-adapted in the laboratory to the sumission substance or the reference substance

Study design

Limit test:
no

Test conditions

Test temperature:
20°C ± 2°C
pH:
7.2 ± 0.2
Nominal and measured concentrations:
nominal concentrations: 250 mg/L, 500 mg/L, 1000 mg/L
Details on test conditions:
TEST SYSTEM
- Test vessel: glass beakers, diameter 60 mm, height 170 mm, volume appr. 480 mL
Reference substance (positive control):
yes
Remarks:
3,5-dichlorophenol: 5, 20, 30 mg/L

Results and discussion

Effect concentrationsopen allclose all
Duration:
3 h
Dose descriptor:
other: EC20
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Duration:
3 h
Dose descriptor:
EC50
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Duration:
3 h
Dose descriptor:
other: EC80
Effect conc.:
> 1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate
Details on results:
The submission substance is not harmful to activated sludge micororganisms. The EC50 is in the range of >1000 mg/L (nominal concentration).
Results with reference substance (positive control):
The EC50 (3 hours) for the reference substance was in the required range of the guideline.
Reported statistics and error estimates:
no data

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Conclusions:
In an activated sludge respiration inhibition test, the submission substance proved to be innooxious to activated sludge microorgansims. The EC50 (3 hours) for respiration inhibition had been determined to be >1000 mg/L.
Executive summary:

In an activated sludge respiration inhibition test, the submission substance proved to be nontoxic to activated sludge microorgansims. The test was conducted according to relevant guidelines. However, documentation is limited (reliability 2). The EC50 (3 hours) for respiration inhibition had been determined to be >1000 mg/L.