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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
27 July 1999 - 24 August 1999
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
EU Method C.4-E (Determination of the "Ready" Biodegradability - Closed Bottle Test)
Deviations:
no
GLP compliance:
yes
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic (adaptation not specified)
Details on inoculum:
Inoculum
-Source of sewage effluent: secondary effluent of a domestic sewage treatment plant (Kläranlage Odenthal)
-Treatment given: separation of coarse particles by filtration
-Concentration of effluents in reaction mixture: 5 mL/L
-Preconditioning: aeration for 4 days
Duration of test (contact time):
28 d
Initial conc.:
4 mg/L
Based on:
test mat.
Parameter followed for biodegradation estimation:
O2 consumption
Details on study design:
The test substance is suspended in a mineral medium, inoculated with a mixed population of aquatic microorganisms and incubated for 28 days under aerobic conditions in the dark at 20 ± 1°C. During this period, the biodegradation of the test substance is determined on the basis of the reduction dissolved oxygen.
Reference substance:
benzoic acid, sodium salt
Remarks:
Purity: 99%; Initail concentration: 2.9 mg/L
Key result
Parameter:
% degradation (O2 consumption)
Value:
3
Sampling time:
28 d
Results with reference substance:
In parallel preparations with the reference substance sodium benzoate a degradation of 73% was achieved within 14 days.

OXYGEN MEASUREMENT

Dissolved oxygen of blank inoculum (mgO₂/L after x days):

Bottle No.

0 days

Bottle No.

7 days

Bottle No.

14 days

Bottle No.

21 days

Bottle No.

28 days

1

2

9.38

9.36

3

4

9.03

9.05

5

6

9.14

9.04

7

8

8.96

9.00

9

10

9.04

9.03

Mean

9.37

 

9.04

 

9.09

 

8.98

 

9.04

 

Dissolved oxygen of reference substance (mgO₂/L after x days):

Bottle No.

0 days

Bottle No.

7 days

Bottle No.

14 days

Bottle No.

21 days

Bottle No.

28 days

11

12

9.29

9.29

13

14

5.69

5.67

15

16

5.47

5.52

17

18

5.42

5.69

19

20

5.62

5.66

Mean

9.29

 

5.68

 

5.50

 

5.56

 

5.64

 

Dissolved oxygen of test substance (mgO₂/L after x days):

Bottle No.

0 days

Bottle No.

7 days

Bottle No.

14 days

Bottle No.

21 days

Bottle No.

28 days

21

22

9.28

9.29

23

24

8.99

9.05

25

26

8.97

8.76

27

28

8.76

8.83

29

30

8.73

8.76

Mean

9.29

 

9.02

 

8.87

 

8.80

 

8.75

 

Dissolved oxygen of toxicity control (mgO₂/L after x days):

Bottle No.

0 days

Bottle No.

7 days

Bottle No.

14 days

Bottle No.

21 days

Bottle No.

28 days

31

32

9.29

9.28

33

34

5.82

5.75

35

36

5.39

5.43

37

38

5.36

5.47

39

40

5.41

5.14

Mean

9.29

 

5.79

 

5.41

 

5.42

 

5.28

 

DO DEPLETION: % DEGRADATION

Test substance

Test concentration: 4.0 mg/L

ThOD: 1745 mg/g

DO Depletion after n days (mg/L)

 

7 d

14 d

21 d

28 d

No. 1: (mt0-mtx) – (mb0-mbx)

0.00

0.03

0.13

0.22

No. 2: (mt0-mtx) – (mb0-mbx)

0.00

0.25

0.07

0.20

D1: % Degradation

0

0

2

3

D2: % Degradation

0

4

1

3

D,Mean

0

2

2

3

 

Reference substance

Test concentration: 2.9 mg/L

ThOD: 1665 mg/g

DO Depletion after n days (mg/L)

 

7 d

14 d

21 d

28 d

No. 1: (mt0-mtx) – (mb0-mbx)

3.27

3.54

3.48

3.34

No. 2: (mt0-mtx) – (mb0-mbx)

3.29

3.49

3.21

3.30

D1: % Degradation

68

73

72

69

D2: % Degradation

68

72

66

68

D,Mean

68

73

69

69

 

Toxicity control*

DO Depletion after n days (mg/L)

 

7 d

14 d

21 d

28 d

No. 1: (mt0-mtx) – (mb0-mbx)

3.14

3.62

3.54

3.55

No. 2: (mt0-mtx) – (mb0-mbx)

3.20

3.57

3.42

3.81

D1: % Degradation

27

31

30

30

D2: % Degradation

27

30

29

32

D,Mean

27

31

30

31

*In the toxicity control 4.0 mg/L test substance and 2.9 mg/L reference substance were used.

Validity criteria fulfilled:
yes
Interpretation of results:
not readily biodegradable
Conclusions:
Within the test period of 28 days, a degradation of 3% was determined for Jasmaprunat. The substance therefore has to be classified as "Not Readily Biodegradable".
Executive summary:

Within the test period of 28 days, a degradation of 3% was determined for Jasmaprunat. The substance therefore has to be classified as "Not Readily Biodegradable".

The method was a closed-bottle test in accordance with Council Directive 92/69 EEC, Method C.4-E

Description of key information

The substance was determined not to be readily biodegradable: attained 3 % degradation after 28 days in a study conducted to EU method C.4-E (closed bottle test).

Key value for chemical safety assessment

Biodegradation in water:
inherently biodegradable, not fulfilling specific criteria
Type of water:
freshwater

Additional information

The substance was determined not to be readily biodegradable and attained 3 % degradation after 28 days in a study conducted to EU method C.4-E (closed bottle test). In an inherent biodegradability study conducted to OECD method 302C, the substance was shown to undergo 43 % biodegradation after 48 days in the test conditions. Biodegradation started on day 3 and reached a plateau at about 40 % on day 11.