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Diss Factsheets

Administrative data

Endpoint:
activated sludge respiration inhibition testing
Type of information:
experimental study
Adequacy of study:
key study
Study period:
26 - 28 October 1999
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP study according to international guidelines.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2000
Report date:
2000

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
GLP compliance:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
liquid: viscous
Details on test material:
Batch: T4649
Expiry date: 23 April 2000
Storage at 10 to 30 dC

Sampling and analysis

Analytical monitoring:
no

Test solutions

Details on test solutions:
Ceraphyl RMT was not soluble in water at concentrations normally used for stock solutions. Therefore, the weighed amounts of substance were directly added to the test medium. The test solutions were subsequently treated with ultra-sonic waves for ten minutes before addition of the inoculum.

Test organisms

Test organisms (species):
activated sludge
Details on inoculum:
Collected from one of the return lines at Burley Menston domestic sewage treatment works (Yorkshire water). The activated sludge had not been adapted or acclimatised to Ceraphyl RMT before exposure.

Study design

Test type:
static
Water media type:
freshwater
Limit test:
yes
Total exposure duration:
3 h

Test conditions

pH:
pH was checked before the start of the test and adjusted to a value between 6 - 8 when it was below 6.
Nominal and measured concentrations:
Nominal: 1.0, 10, 100 and 1000 mg/L
Details on test conditions:
All mixtures tested comprised 16 mL synthetic sewage diluted to 300 mL. Inoculation entailed addition of 200 mL activated sludge.
Before measurements the DO-meter was calibrated at 0 and 100% saturation. At the end of the 3-h incubation, a portion of the first test mixture was transferred to fill a clean 250 mL sample bottle containing a stirrer bar. The dissolved oxygen was measured at 15-minute intervals with the DO-meter under continuous stirring. Respiration rates were subsequently derived from tthe longest linear portion of each valid trace.
Reference substance (positive control):
yes
Remarks:
3,5-dichlorophenol

Results and discussion

Effect concentrationsopen allclose all
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:
NOEC
Effect conc.:
1 000 mg/L
Nominal / measured:
nominal
Conc. based on:
test mat.
Basis for effect:
inhibition of total respiration
Remarks:
respiration rate

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Remarks:
The control respiration rates used to obtain the mean lay within 15% of each other. The EC50 of the reference inhibitor was between 5 and 30 mg/L, the limits for acceptance of the reference test.
Conclusions:
The test substance has proven to be non-toxic to fresh-water micro-organisms at levels below, at and above its solubility in water.