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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:
2017
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 B (Ready Biodegradability: CO2 Evolution Test)
Deviations:
no
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method C.4-C (Determination of the "Ready" Biodegradability - Carbon Dioxide Evolution Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Specific details on test material used for the study:
Name: Poly(oxy-1,2-ethanediyl), .alpha.,.alpha.'-(iminodi-2,1-ethanediyl)bis[.omega.-hydroxy-, N-[3-(C10-16-alkyloxy)propyl] derivs., di-Et sulfate-quaternized
Product Description: C10-16-alkyletherpropylamine, ethoxylated, DES Quat
CAS No.: 70983-58-3
Physical state: yellowish to amber viscous liquid at 20 °C
Batch No.: PFS-755-173
Re-certification date of batch: 19 April 2018
Purity: 100 % (UVCB)
Color, Gardner 8.8
pH, 5% in water 5.76
Acid Value , mg KOH/g 20.1
Moisture, % 0.127
Total Amine, mg/g 11.18
Viscosity,cps, #4@60,25C 3280
Appearance @25C pass
Stability: stable under test conditions
Storage condition of test material: Room temperature, protected from light
Oxygen conditions:
aerobic
Inoculum or test system:
sewage, predominantly domestic, non-adapted
Details on inoculum:
Activated sludge from the municipal wastewater treatment plant Breisgauer Bucht was used as inoculum with a concentration corresponding to 30 mg dry solids per litre. The treatment plant clarifies predominantly domestic wastewater and has a capacity of 600.000 inhabitant equivalents. Sampling date of activated sludge was on 4 July 2017. The dry solid content of the activated sludge was 3.9 g/L. It was determined by weight measurements after drying at 105°C for 5 hours (mean of triplicate measurements). The activated sludge was washed twice with tap water by settling the sludge, decanting the supernatant and re-suspending the sludge.
Duration of test (contact time):
28 d
Initial conc.:
20 mg/L
Based on:
TOC
Parameter followed for biodegradation estimation:
CO2 evolution
Reference substance:
benzoic acid, sodium salt
Key result
Parameter:
% degradation (CO2 evolution)
Value:
-0.3
Sampling time:
28 d
Details on results:
No degradation of the test item could be observed within the test duration. The degradation at the end of the test was -0.3% (28 d after acidification, mean of two replicates). The test item did not reach the criteria for ready biodegradability (60% of ThCO2 within a 10-d window). The degradation of the toxicity control after 14 days was 39.3%. The test item had no inhibitory effect on the inoculum according to the criterion of the guideline.
Results with reference substance:
The reference compound sodium benzoate reached the pass levels for ready biodegradability within 4 days.

Table 1: Ultimate biodegradation after x days [% of ThCO2]

 reactor  day  0  4  7  11  14  21  28  29
 11  Test flasks  0  -1.8  5.8  4.4  4.2  4.3  2.9  2.3
 12    0  -3.6  0.6  1.1  0.5  -1.4  -2.6  -2.9
 13*    0  -0.4  5.3  5.7  7.1  10.6  17.5  18.0
 4  Reference flasks  0  75.4  86.3  88.4  89.5  90.6  93.1  96.8
 5

 0

 77.7

 82.7

 84.7

 87.1

 86.0

 90.4

 94.6

 6

 

 0

 72.8

 80 .7

 86.7

 87.8

 87.6

 88.9

 91.8

 14

 Toxicity control - test item & reference item

 0

 32.1

 37.7

 40.7

 39.3

 40.4

 41.4

 41.4

* outlier

Table 2: Mean CO2 evolution of blanks after x days

 Day  0  4  7  11  14  21  28  29
 CO2 -evolution [mg/l]  0  9.6  14.2  18.5  21.7  25.6  30.5  31.6
Validity criteria fulfilled:
yes
Remarks:
The temperature during the test was 19.2 – 22.3°C and therefore below the range required by the guideline (22 ± 2°C). The underrun of the required temperature occurred between day 15 and day 20 of the study and was therefore only temporarily.
Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
No degradation of the test item could be observed within the test duration. The degradation at the end of the test was -0.3% (28 d after acidification, mean of two replicates). The test item did not reach the criteria for ready biodegradability (60% of ThCO2 within a 10-d window). The degradation of the toxicity control after 14 days was 39.3%. The test item had no inhibitory effect on the inoculum according to the criterion of the guideline.
Executive summary:

In a Klimisch 1 OECD 301 B GLP study no degradation of the test item could be observed within the test duration. The degradation at the end of the test was -0.3% (28 d after acidification, mean of two replicates). The test item did not reach the criteria for ready biodegradability (60% of ThCO2 within a 10-d window). The degradation of the toxicity control after 14 days was 39.3%. The test item had no inhibitory effect on the inoculum according to the criterion of the guideline.

Description of key information

No degradation of the test item could be observed within the test duration. The degradation at the end of the test was -0.3% (28 d after acidification, mean of two replicates). The test item did not reach the criteria for ready biodegradability (60% of ThCO2 within a 10-d window). The degradation of the toxicity control after 14 days was 39.3%. The test item had no inhibitory effect on the inoculum according to the criterion of the guideline.

Key value for chemical safety assessment

Biodegradation in water:
under test conditions no biodegradation observed

Additional information