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EC number: 701-281-9 | CAS number: -
Biodegradation in water: screening tests
Administrative data
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 16 December 2009 - 27 April 2010
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: GLP study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 E (Ready biodegradability: Modified OECD Screening Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 185146-18-2
- IUPAC Name:
- 185146-18-2
- Details on test material:
- - Name of test material (as cited in study report): "3-HYDROXY-2-(HYDROXYMETHYL)-2-METHYLPROPIONALDEHYDE"
- Molecular formula (if other than submission substance):C5H10O3
- Lot No.: CH 138067/001.
- CAS No.: 185146-18-2.
- Appearance: uncolored and high viscous.
- Purity test date:
~ 82 % Dimethylpropanale
~ 10 % Hydroxymethanesulfonic acid, Na-salt (CAS No: 870-72-4)
~ 6 % water *)
~ 2 % Potassiumformiate (CAS No: 590-29-4).
- Solubility: In water: Soluble
- pH: 7.25.
- Conditions of storage: Room temperature.
- Stability at conditions of storage: Min. 1 year.
- Expiry date: 30 November 2010.
*) The results presented in the report refer to the dry weight of the test substance not including the 6 % water content.
Constituent 1
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- other: effluent of a sewage treatment plant
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): effluent from a sewate treatment plant, A-2451 Au am Leithagebirge
- Storage conditions: The effluent was aerated by means of filtered compressed air for about 10 minutes before being used for the study
- Preparation of inoculum for exposure: The number of cells of the effluent was determined. Each flask was inoculated with 0.5 mL sewage effluent with approximately 3 000 000 cells per mL
- Pretreatment: None.
- Initial cell/biomass concentration: approx. 1 500 000 cells per vessel - Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 20 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: Mineral medium as described in the guidelines
- Additional substrate: None.
- Solubilising agent (type and concentration if used): Not used
- Test temperature: mean temperature: 20.6 °C
- pH: Day 0: 7.4 - 7.5, Day 28: 7.1 - 7.3
- pH adjusted: No.
- Aeration of dilution water: No.
- Suspended solids concentration: Not applicable
- Continuous darkness: Yes.
TEST SYSTEM
- Culturing apparatus: 2L conical flask reaction vessel filled with 1 000 mL test medium.
- Number of culture flasks/concentration: 2 negative control flasks, 2 test substance flask, 1 positive control, 1 toxicity control, 1 abiotic steril control, 1 adsorption control
- Method used to create aerobic conditions: the opening of the vessels was covered with aluminium foil in such a way that the exchang of air was guaranteed.
- Measuring equipment: Measurements were performed with a carbon analyser (TOC-Analysator multi N/C 2000, Analytik Jena).
SAMPLING
- Sampling frequency: Day 0, 2, 4, 7, 10, 14, 17, 21, 24, and 28. Abiotic steril control and adsorption control were determined only on day 28.
- Sampling method: DOC concentrations were determined from the supernatants.
- Sample storage before analysis: Samples were analysed on the same day.
CONTROL AND BLANK SYSTEM
- Inoculum blank: Yes
- Abiotic sterile control: Yes.
- Toxicity control: Yes.
- Other: Adsorption control
STATISTICAL METHODS: no.
Reference substance
- Reference substance:
- benzoic acid, sodium salt
Results and discussion
- Preliminary study:
- None.
% Degradation
- Parameter:
- % degradation (DOC removal)
- Value:
- 11.2
- Sampling time:
- 28 d
BOD5 / COD results
- Results with reference substance:
- The plateau of biodegradation was reached on Day 4 and the degradation of sodium benzoate exceeded the pass level of 70 % within 14 days
Any other information on results incl. tables
Validity of the test:
The test is considered valid if the difference of extremes of replicate values of the removal of the test substance at the plateau, at the end of the test or at the 10-d window, as appropriate, is less than 20 % and if the percentage degradation of the reference compound has reached the pass levels by day 14.
These criteria were fulfilled.
Percent biodegradation
|
test substance |
positive control |
toxicity control |
||
Day |
A33 |
A34 |
mean |
PK5 |
TK36 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
3.48 |
2.71 |
3.10 |
86.61 |
47.70 |
4 |
5.07 |
5.98 |
5.52 |
94.68 |
52.86 |
7 |
5.67 |
7.04 |
6.35 |
95.06 |
52.52 |
10 |
29.97 |
16.43 |
23.20 |
100.17 |
56.67 |
14 |
10.74 |
10.03 |
10.38 |
95.96 |
53.45 |
17 |
- *) |
2.49 |
- *) |
98.59 |
- *) |
21 |
10.82 |
10.83 |
10.83 |
98.03 |
55.97 |
24 |
12.96 |
11.81 |
12.39 |
96.97 |
57.24 |
28 |
17.54 |
4.80 |
11.17 |
99.20 |
62.83 |
*)During centrifugation of the day 17 samples the vessels of the individual samples A33 and TK36 broke. Therefore no DOC analysis of these samples could be performed.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- The test substance can not be classified as readily biodegradable.
- Executive summary:
Aim and methods
The ready biodegradability of"3-HYDROXY-2-(HYDROXYMETHYL)-2-METHYLPROPIONALDEHYDE"was determined by the measurement of DOC (dissolved organic carbon) at frequent intervals over a 28 d period. The method used was that described in Part C.4-B of the Regulation (EC) 440/2008 and in the OECD Guideline 301 E.
Results
· The reference substance sodium benzoate was degraded by 96.0 % within 14 days.
· Degradation in the toxicity control, which contained sodium benzoate and the test substance, was not indicative of an inhibition of the microbial activity by the test substance.
· The test substance"3-HYDROXY-2-(HYDROXYMETHYL)-2-METHYLPROPIONALDEHYDE"with a nominal starting concentration of 20 mg DOC/L was not degraded within 28 days of incubation at a mean temperature of 20.6 °C.
Classification
According to the Guidelines a substance giving a result greater than 70 % loss of DOC in a
10-d window within 28 days is regarded as "readily biodegradable".According to the results of this study,"3-HYDROXY-2-(HYDROXYMETHYL)-2-METHYLPROPIONALDEHYDE"can therefore not be classifiedas readily biodegradable.
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