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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Reference
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
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 D (Ready Biodegradability: Closed Bottle Test)
Deviations:
no
GLP compliance:
yes
Oxygen conditions:
aerobic
Inoculum or test system:
sewage, predominantly domestic, non-adapted
Remarks:
Secondary effluent from a domestic sewage treatment plant
Details on inoculum:
- Source of inoculum/activated sludge: municipal sewage treatment plant Hochdahl
- Storage conditions: not reported
- Storage length: not reported
- Preparation of inoculum for exposure: not reported
- Pretreatment: not reported
- Concentration of inoculum: one drop per litre of mineral medium
Duration of test (contact time):
28 d
Initial conc.:
2 mg/L
Based on:
test mat.
Initial conc.:
5 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation:
O2 consumption
Details on study design:
TEST CONDITIONS
- Composition of medium: not reported
- Additional substrate: no
- Solubilising agent (type and concentration if used): yes, but not specified
- Test temperature: 20 ± 1 °C
- pH: not reported
- pH adjusted: no
- Aeration of dilution water: yes, prior to test
- Suspended solids concentration: not applicable
- Continuous darkness: yes

TEST SYSTEM
- Number of culture flasks/concentration: 10
- Method used to create aerobic conditions: aeration of test water
- Measuring equipment: iodometric determination of oxygen concentration
- Test performed in closed vessels due to significant volatility of test substance: yes

SAMPLING
- Sampling frequency: weekly

CONTROL AND BLANK SYSTEM
- Inoculum blank: yes
- Toxicity control: no
- Other: solvent control
Reference substance:
benzoic acid, sodium salt
Parameter:
% degradation (O2 consumption)
Value:
60
Sampling time:
7 d
Remarks on result:
other: Obtained with 2 mg/L
Key result
Parameter:
% degradation (O2 consumption)
Value:
86
Sampling time:
28 d
Remarks on result:
other: Obtained with 2 mg/L
Key result
Parameter:
% degradation (O2 consumption)
Value:
62
Sampling time:
28 d
Remarks on result:
other: Obtained with 5 mg/L
Details on results:
The concentration of dissolved oxygen fell below 0.5 mg/L at the 5 mg/L test concentration, which should normally be avoided according to the validity criteria of the test. However, no such effect was seen at the lower test concentration of 2 mg/L, which is given as the generally applicable test concentration for the closed bottle test (see OECD guideline 301-D).
Results with reference substance:
The test with the positive reference substance sodium benzoate gave a degradation of 84% after 2 weeks and a degradability of 90% after 28 days. This test demonstrated the suitability of the test system.
Validity criteria fulfilled:
yes
Remarks:
for the lower test concentration of 2 mg/L; for the higher test concentration the oxygen demand was too high leading to an unacceptable depletion in the dissolved oxygen concentration
Interpretation of results:
readily biodegradable
Conclusions:
The substance was readily biodegradable in the closed bottle test and the 10-day window was fulfilled.
Executive summary:

The ready biodegradability of the test substance allylcyclohexylpropionate was studied under GLP in accordance with OECD TG 301-D in a closed bottle test. Secondary effluent from a municipal treatment plant processing mainly domestic sewage was used as inoculum. The tests were performed with concentrations of the test substance at 2 mg/L and 5 mg/L and a concentration of one drop of inoculum per L mineral medium. An unknown solvent was used to dissolve the poorly water-soluble substance. The dissolved oxygen concentration (DOC) in the test medium was maximised by vigorously aerating the mineral medium prior to the test and the DOC was 9.14 mg/L at the beginning of the test. Tightly closed bottles were incubated in the dark at a temperature of 20 ± 1 °C for 28 days. The oxygen consumption was determined every 7 days by iodometric measurement and the percentage of degradation was calculated by comparing the measured oxygen consumption with the theoretical consumption. With 2 mg/L test concentration, 60% degradation was obtained after 7 days and 86% degradation was obtained after 28 days. A significant depletion in the DOC below 0.5 mg/L was seen with 5 mg/L test concentration at the third sampling timepoint. This was obviously due to a too high oxygen consumption at this concentration and this test was not fulfilling the validity criteria. A parallel test with the reference substance sodium benzoate gave 81% degradation after 7 days and 84% degradation after 14 days showing the suitability of the test system and inoculum. Based on the test with 2 mg/L test concentration, the substance was considered as readily biodegradable fulfilling the 10-day window.

Description of key information

Readily biodegradable

Key value for chemical safety assessment

Biodegradation in water:
readily biodegradable
Type of water:
freshwater

Additional information

A valid closed bottle test using 2 mg/L test substance according to OECD TG 301-D demonstrated the ready biodegradability of allyl 3-cyclohexylpropionate (86% degradation, 10-day window fulfilled).