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Environmental fate & pathways

Biodegradation in water: screening tests

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Endpoint:
biodegradation in water: ready biodegradability
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1988
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 E (Ready biodegradability: Modified OECD Screening Test)
Qualifier:
according to guideline
Guideline:
EU Method C.4-B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test)
GLP compliance:
yes
Specific details on test material used for the study:
Details on properties of test surrogate or analogue material:
PHYSICO-CHEMICAL PROPERTIES
- Melting point: > 320°C
- Boiling point: NA
- Vapour pressure: NA
- Henry's law constant (for volatie substances): NA
- Water solubility (under test conditions): ca 171 g/l (corrected for purity)
- Solubility in organic solvents: NA
- log Pow: ca. 7.1
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: Kommunale Kläranlage Frankfurt-Sindlingen
- Preparation of inoculum for exposure:
- Pretreatment: according to directive section 1.6.3.1
- Concentration of sludge: according to directive section 1.6.4
Duration of test (contact time):
28 d
Initial conc.:
110 mg/L
Based on:
test mat.
Initial conc.:
39.02 mg/L
Based on:
DOC
Parameter followed for biodegradation estimation:
DOC removal
Parameter:
% degradation (DOC removal)
Value:
30 - 40
Sampling time:
28 d
Details on results:
pH during test phase: 6.5 to 7.6
The biotic degradation of the test-substance remained clearly below 70% lying between 30% to 40%. It is therefore considered not to be readily biodegradable.
It cannot be excluded that ultimate biodegradation (inherent biodegradation) takes place.
A fraction of about 20% was eliminated via absorption to the biomass.
Results with reference substance:
Degradation of reference substance is above 80%
Validity criteria fulfilled:
yes
Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
The biotic degradation of the test-substance remained clearly below 70% lying between 30% to 40%. It is therefore considered not to be readily biodegradable.
It cannot be excluded that ultimate degradation (inherent biodegradation) takes place.
A fraction of about 20% was eliminated via absorption to the biomass.
Endpoint:
biodegradation in water: ready biodegradability
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Study period:
1988
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
Please refer to Section 13
Reason / purpose for cross-reference:
read-across source
Qualifier:
according to guideline
Guideline:
OECD Guideline 301 E (Ready biodegradability: Modified OECD Screening Test)
Qualifier:
according to guideline
Guideline:
EU Method C.4-B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test)
GLP compliance:
yes
Specific details on test material used for the study:
Details on properties of test surrogate or analogue material:
PHYSICO-CHEMICAL PROPERTIES
- Melting point: > 320°C
- Boiling point: NA
- Vapour pressure: NA
- Henry's law constant (for volatie substances): NA
- Water solubility (under test conditions): ca 171 g/l (corrected for purity)
- Solubility in organic solvents: NA
- log Pow: ca. 7.1
Oxygen conditions:
aerobic
Inoculum or test system:
activated sludge, domestic, non-adapted
Details on inoculum:
- Source of inoculum/activated sludge: Kommunale Kläranlage Frankfurt-Sindlingen
- Preparation of inoculum for exposure:
- Pretreatment: according to directive section 1.6.3.1
- Concentration of sludge: according to directive section 1.6.4
Duration of test (contact time):
28 d
Initial conc.:
110 mg/L
Based on:
test mat.
Initial conc.:
39.02 mg/L
Based on:
DOC
Parameter followed for biodegradation estimation:
DOC removal
Parameter:
% degradation (DOC removal)
Value:
30 - 40
Sampling time:
28 d
Details on results:
pH during test phase: 6.5 to 7.6
The biotic degradation of the test-substance remained clearly below 70% lying between 30% to 40%. It is therefore considered not to be readily biodegradable.
It cannot be excluded that ultimate biodegradation (inherent biodegradation) takes place.
A fraction of about 20% was eliminated via absorption to the biomass.
Results with reference substance:
Degradation of reference substance is above 80%
Validity criteria fulfilled:
yes
Interpretation of results:
under test conditions no biodegradation observed
Conclusions:
The biotic degradation of the test-substance remained clearly below 70% lying between 30% to 40%. It is therefore considered not to be readily biodegradable.
It cannot be excluded that ultimate degradation (inherent biodegradation) takes place.
A fraction of about 20% was eliminated via absorption to the biomass.

Description of key information

The biotic degradation of the test-substance remained clearly below 70% lying between 30% to 40%. It is therefore considered not to be readily biodegradable.
It cannot be excluded that ultimate biodegradation (inherent biodegradation) takes place.
A fraction of about 20% was eliminated via absorption to the biomass.

Key value for chemical safety assessment

Biodegradation in water:
not biodegradable
Type of water:
freshwater

Additional information