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Environmental fate & pathways

Biodegradation in water: screening tests

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Reference
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Study period:
From 17 October to 14 November 2019
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: Cambridge STW, Cowley Road, Cambridge
- Preparation of inoculum for exposure: Sieved to 850μm, settled, decanted and re-suspended using mineral media. Centrifuged at 4000rpm for 10 minutes discarding the supernatant, re-suspended and centrifuged again at 4000rpm for 10 minutes and discarding the supernatant. Dry sludge solids determination was conducted on the pellet produced.
- Concentration of sludge: 0.0299g/L dry sludge solids in test
Duration of test (contact time):
28 d
Initial conc.:
9.9 mg/L
Based on:
ThOD
Parameter followed for biodegradation estimation:
O2 consumption
Details on study design:
TEST CONDITIONS
- Composition of medium: The mineral medium was prepared by the addition of mineral nutrient stock solutions to deionised water.
- Test temperature: 20.4 – 22.8°C
- pH: At test termination the pH of the reference replicates reached 8.73 and 8.88, the toxicity control also reached 9.07.
- pH adjusted: no

TEST SYSTEM
- Number of culture flasks/concentration: 2
- Measuring equipment: The BOD of the test solutions is monitored using the OXITOP® Control OC 110 controller in conjunction with the OXITOP® Control 12 measuring heads. All generated data is manipulated using the communication software ACHAT OC.

SAMPLING
Not applicable: The OXITOP® measuring heads recorded readings of biodegradation every 112 minutes for 28 days.

CONTROL AND BLANK SYSTEM
- Inoculum blank: Included
- Abiotic sterile control: Not included
- Toxicity control: Included
Reference substance:
acetic acid, sodium salt
Parameter:
% degradation (O2 consumption)
Value:
45
Sampling time:
7 d
Parameter:
% degradation (O2 consumption)
Value:
61
Sampling time:
14 d
Parameter:
% degradation (O2 consumption)
Value:
70
Sampling time:
21 d
Parameter:
% degradation (O2 consumption)
Value:
74
Sampling time:
28 d
Details on results:
Reaction Mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) did not achieve the 10-day window since a degradation > 60% (relative to the ThOD value) was not reached until Day 13
Parameter:
ThOD
Value:
3 029 mg O2/g test mat.
Validity criteria fulfilled:
yes
Interpretation of results:
readily biodegradable, but failing 10-day window
Conclusions:
Reaction mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) was degraded at 74% after 28 days but failed to meet the 10-day window.
Executive summary:

The ready biodegradability Reaction mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) was evaluated during a GLP-compliant study performed in accordance with the OECD Testing Guideline 301F (Manometric Respirometry).

The test was performed in closed vessels containing a known concentration of test item in inoculated medium incubated at constant temperature for 28 days. The percent of biodegradation of the test item was calculated based on the Theoretical Oxygen Demand (ThOD) of 3029 mg O2/g test item calculated for the test substance. Oxygen consumption was evaluated through the study.

Sodium acetate was used as reference substance.

The mean biodegradation value of the test item at the end of the test period, on Day 28, was 74% of the ThOD.

Validation criteria were met. A toxicity control indicated that the test substance had no inhibitory effect on the activity of activated sludge microorganisms at the tested concentration of 9.9 mg/L.

Reaction mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) was found to be readily biodegradable under the test conditions within 28 days, but failed to meet the 10-day window.

Description of key information

The ready biodegradability Reaction mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) was evaluated during a GLP-compliant study performed in accordance with the OECD Testing Guideline 301F (Manometric Respirometry).

The test was performed in closed vessels containing a known concentration of test item in inoculated medium incubated at constant temperature for 28 days. The percent of biodegradation of the test item was calculated based on the Theoretical Oxygen Demand (ThOD) of 3029 mg O2/g test item calculated for the test substance. Oxygen consumption was evaluated through the study.

Sodium acetate was used as reference substance.

The mean biodegradation value of the test item at the end of the test period, on Day 28, was 74% of the ThOD.

Validation criteria were met. A toxicity control indicated that the test substance had no inhibitory effect on the activity of activated sludge microorganisms at the tested concentration of 9.9 mg/L.

Reaction mass of 2-Propenoic acid, 2-methyl-, 2-dodecylhexadecyl ester and 2-Propenoic acid, 2-methyl-, 2-tetradecyloctadecyl ester (EC 946-978-0) was found to be readily biodegradable under the test conditions within 28 days, but failed to meet the 10-day window.

Key value for chemical safety assessment

Biodegradation in water:
readily biodegradable but failing 10-day window
Type of water:
freshwater

Additional information