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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Referenceopen allclose all

Endpoint:
biodegradation in water: ready biodegradability
Type of information:
other: expert judgement based on available data
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
accepted calculation method
Guideline:
other: REACH Guidance on QSARs R.6
Inoculum or test system:
other: expert judgement
Parameter:
probability of ready biodegradability (QSAR/QSPR)
Remarks on result:
not readily biodegradable based on QSAR/QSPR prediction
Validity criteria fulfilled:
not applicable
Remarks:
estimation by EPI Suite and QSAR
Interpretation of results:
not readily biodegradable
Conclusions:
Based on prediction carried out with EPI Suite and QSAR, the substance resulted as non ready biodegradable.
Executive summary:

Method

Estimation of probability of rapid biodegradation relying on EPI Suite and QSAR dyes. The overall assessment is based on the responses given by different predictive models for biodegradability under various conditions: linear and non-linear models, ultimate and primary survey models, MITI linear and non-linear models, anaerobic linear model.

Results

The substance was predicted to be not ready biodegradable.

Endpoint:
biodegradation in water: ready biodegradability
Remarks:
prediction
Type of information:
(Q)SAR
Adequacy of study:
supporting study
Study period:
2020
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
accepted calculation method
Justification for type of information:
QSAR estimation
Qualifier:
no guideline required
Principles of method if other than guideline:
QSAR dyes R&C report produced by version QSAR dyes RC 2.0 Developed by Milano Chemometrics and QASR research group Dept. Earth and Environmental Science, University Milano
Bicocca, Italy.
Parameter:
probability of ready biodegradability (QSAR/QSPR)
Remarks on result:
not readily biodegradable based on QSAR/QSPR prediction
Validity criteria fulfilled:
not applicable
Remarks:
estimation by prediction tool
Interpretation of results:
not readily biodegradable
Conclusions:
Based on prediction carried out with the prediction tool, the substance resulted as non ready biodegradable.
Executive summary:

Results

The substance was predicted to be not ready biodegradable.

Endpoint:
biodegradation in water: inherent biodegradability
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
From the 15th of July to the 31th of August, 1994
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
Deviations:
no
Principles of method if other than guideline:
Internal method SAV: 13 000 03
GLP compliance:
yes (incl. QA statement)
Inoculum or test system:
activated sludge, domestic (adaptation not specified)
Details on inoculum:
Sludge from Ara Reinach communal sewage treatment plant, collected on 02/08/1994
Duration of test (contact time):
28 d
Details on study design:
TEST CONDITIONS- Test temperature: 22.0 ± 3°C (room temperature)- Lighting: indirect daylight- Test concentrations: 150 mg/L DOC nominal
Reference substance:
diethylene glycol
Preliminary study:
A preliminary study was performed
Parameter:
other: DOC
Value:
5.3
Sampling time:
28 d
Remarks on result:
other: everage of 2 tests running in parallel
Parameter:
other: adsorption
Value:
6.3
Sampling time:
3 h
Details on results:
The biodegradation value has been corrected by the blank control.See table 1 attached for further details on data.
Results with reference substance:
DOC (mg/l) is: 99.5 % 8th day (average of 2 tests running in parallel).Corrected by the blank control and measured.
Validity criteria fulfilled:
not specified
Interpretation of results:
not inherently biodegradable
Conclusions:
The biodegradation of the test substance Acid Red 249 after 28 days was 5.3 % while the biodegradation of the reference substance after 8 days was 99.5 %.
Executive summary:

The inherent biodegradability of the substance was determined in a Zahn-Wellens, test according to the OECD Guideline for Testing of Chemicals, No. 302B, Paris 1992. The test has been performed in compliance with the Procedures and Principles of Good Laboratory Practice (March 1986) issued by the Swiss Federal Department of the Interior recognizing the " OECD Principles of Good Laboratory Practice " Paris, 1981. The test substance Acid Red 249 and the reference substance Diethylenglycol, respectively, were tested in concentrations of 150 mg/l DOC.

The biodegradation of the test substance after 28 days was 5.3 % while the biodegradation of the reference substance after 8 days was 99.5 %.

Endpoint:
biodegradation in water: screening tests
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
The 13th of September 1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Test not performed under GLP Guideline. Internal method were used, but not detailed.
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
Internal Method A.16
GLP compliance:
no
Remarks:
Pre GLP.
Inoculum or test system:
not specified
Remarks on result:
not determinable
Parameter:
BOD5
Value:
ca. 0 mg O2/g test mat.
Key result
Parameter:
BOD5*100/COD
Value:
ca. 0 other: n.a.

Concentration: 500 mg/L

Validity criteria fulfilled:
not specified
Conclusions:
BOD of the test substance is 0 mg/g O2. The calculated Biodegradability index" (B.I.)., BOD5/COD is 0.
Executive summary:

BOD5 was measured according to Method A-15. Details of the method have been not reported.

The BOD measured was 0 mg/g O2, at concentration of 500 mg/L.

The calculated Biodegradability index" (B.I.)., BOD5/COD is 0.

Endpoint:
biodegradation in water: screening tests
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
The 13th of September 1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Test not performed under GLP Guideline. Internal method were used, but not detailed.
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
Internal method A.16
GLP compliance:
no
Remarks:
Pre GLP.
Inoculum or test system:
not specified
Remarks on result:
not determinable
Parameter:
COD
Value:
ca. 1 087 mg O2/g test mat.
Key result
Parameter:
BOD5*100/COD
Value:
0

Concentration: 5 mg/L

Validity criteria fulfilled:
not specified
Conclusions:
COD of the test substance is 1087 mg/g O2. The calculated Biodegradability index" (B.I.)., BOD5/COD is 0.
Executive summary:

COD was measured according to Method A-16. Details of the method have been not reported.

The COD measured was 1087 mg/g O2, at concentration of 5 mg/L.

The calculated Biodegradability index" (B.I.)., BOD5/COD is 0.

Description of key information

Based on expert judgement and QSAR prediction the substance is not readily biodegradable.

Additional tests for the evaluation of inherent biodegradability and BOD/COD evalutaion of the substance itself are available with weight of evidence approach.

Inherent biodegradability: the biodegradation of the test substance after 28 days was 5.3 % while the biodegradation of the reference substance after 8 days was 99.5 %.
COD: 1087 mg/g O2, at concentration of 5 mg/L.
BOD5: 0 mg/g O2, at concentration of 500 mg/L.
BOD5/COD: 0

Key value for chemical safety assessment

Biodegradation in water:
not biodegradable

Additional information

Based on expert judgement and QSAR prediction the substance is not readily biodegradable.

Different available tests may be valuable, as part of a Weight of Evidence approach that gives information on biodegradability.

Inherent biodegradability

The inherent biodegradability was determined in a Zahn-Wellens, test according to the OECD Guideline for Testing of Chemicals, No. 302B, Paris 1992. The test has been performed in compliance with the Procedures and Principles of Good Laboratory Practice (March 1986) issued by the Swiss Federal Department of the Interior recognizing the " OECD Principles of Good Laboratory Practice " Paris, 1981. The test substance and the reference substance Diethylenglycol, respectively, were tested in concentrations of 150 mg/l DOC.

The biodegradation of the test substance after 28 days was 5.3 % while the biodegradation of the reference substance after 8 days was 99.5 %.

COD/BOD5 ratio

Biochemical Oxygen Demand (BOD5) and Chemical Oxygen Demand (COD) are the most commonly used parameters for the characterization of the biodegradability capacity.

COD results are typically higher than BOD5 values, and the ratio between vary depending on the characteristics of the substrate. This ratio has been commonly used as an indicator for biodegradation capacity, the "Biodegradability index" (B.I.).

Studies on BOD5 and COD are available for this substance, therefore they have been used together with the inherent biodegradability OECD 302.B.

in the weight of evidence approach for this substance.

COD was measured according to Method A-16. Details of the method have been not reported. The COD measured was 1087 mg/g O2, at concentration of 5 mg/L.

BOD5 was measured according to Method A-15. Details of the method have been not reported. The BOD5 measured was 0 mg/g O2, at concentration of 500 mg/L.

The ratio BOD5/COD is 0.