Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Environmental fate & pathways

Biodegradation in water: screening tests

Currently viewing:

Administrative data

Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992
Report date:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method C.4-B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test)
Version / remarks:
Cited as Directive 84/449/EEC, C.3
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2,6,6-tetramethyl-4-piperidone
EC Number:
212-554-2
EC Name:
2,2,6,6-tetramethyl-4-piperidone
Cas Number:
826-36-8
Molecular formula:
C9H17NO
IUPAC Name:
2,2,6,6-tetramethylpiperidin-4-one

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic (adaptation not specified)
Details on inoculum:
- Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): municipal STP, Marl-Ost
- Water filtered: yes
Duration of test (contact time):
28 d
Initial test substance concentration
Initial conc.:
11.6 mg/L
Based on:
DOC
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
DOC removal
Details on study design:
TEST CONDITIONS
- Composition of medium: 2 mL mineral nutrient solution, 2 mL micronutrients solution, 2 mL vitamin solution, 1 mL inoculum, test item solution resulting in approx. 10 mg DOC/L, water added up to a volume of 2 L
- Test temperature: 25-25.1°C
- pH adjusted: no data
- Continuous darkness: yes

TEST SYSTEM
- Number of culture flasks/concentration: 2
- Number of inoculum blank samples: 2
- Number of reference substance samples: 2
Reference substance
Reference substance:
benzoic acid, sodium salt

Results and discussion

% Degradation
Parameter:
% degradation (DOC removal)
Value:
11
Sampling time:
28 d
Details on results:
Kinetic of test substance (in % DOC reduction):
7% after 7 day(s)
11% after 14 day(s)
4% after 21 day(s)
7% after 27 day(s)
11% after 28 day(s)

BOD5 / COD results

Results with reference substance:
Kinetic of control substance (in % DOC reduction):
98% after 14 day(s)
100% after 28 day(s)

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Interpretation of results:
other: not readily biodegradable
Conclusions:
In this screening test for ready degradability the test item triacetonamine showed a degradation of 11% after 28 days.