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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Environmental fate & pathways

Biodegradation in water: screening tests

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:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2017

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Enoxolone
EC Number:
207-444-6
EC Name:
Enoxolone
Cas Number:
471-53-4
Molecular formula:
C30H46O4
IUPAC Name:
3-hydroxy-11-oxoolean-12-en-30-oic acid
Test material form:
solid: particulate/powder

Study design

Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, adapted
Details on inoculum:
Activated sludge from a biologic sewage treatment plant was used as inoculum. The cho-sen plant is treating mostly domestic sewage.
Duration of test (contact time):
28 d
Initial test substance concentration
Initial conc.:
20 mg/L
Based on:
ThCO2
Parameter followed for biodegradation estimation
Parameter followed for biodegradation estimation:
CO2 evolution

Results and discussion

% Degradationopen allclose all
Key result
Parameter:
% degradation (CO2 evolution)
Value:
73
Sampling time:
10 d
Key result
Parameter:
% degradation (CO2 evolution)
Value:
84
Sampling time:
28 d

Applicant's summary and conclusion

Validity criteria fulfilled:
yes
Interpretation of results:
readily biodegradable
Conclusions:
All validity criteria were met.
Degradation behaviour of positive control and toxicity control was normal. Abiotic degradation was not observed. Both replicates of the test item showed very good correspondence.
If degradation in the toxicity flask is below 25 % after 14 days, the test item can be consid-ered as toxic towards the inoculum. As degradation in the toxicity flask was 79.3 % after 14 days, the test item can be stated as “not toxic towards the inoculum in a concentration of 26.3 mg/L”.
Ready biodegradability is defined in the guidelines as degradation surpassing 60% within 10 days after reaching a level of 10 %. Therefore, the test item Enoxolone can be considered as “readily biodegradable”.
No observations were made which might cause doubts concerning the validity of the study outcome.
The result of the test can be considered valid.