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EC number: 275-033-9 | CAS number: 70942-15-3
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Biodegradation in water: screening tests
Administrative data
Link to relevant study record(s)
- Endpoint:
- biodegradation in water: inherent biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- From May 31 to June 28, 1995
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study without detailed documentation
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 302 B (Inherent biodegradability: Zahn-Wellens/EMPA Test)
- Deviations:
- no
- Principles of method if other than guideline:
- Analysis conducted with internal method SAV: 13 000 03
- GLP compliance:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge: Activated sludge of a communal sewage treatment plant Ara Reinach collected on 30.05.95
- Concentration of sludge: 530 mg/l - Duration of test (contact time):
- ca. 28 d
- Initial conc.:
- ca. 150 mg/L
- Based on:
- DOC
- Details on study design:
- TEST CONDITIONS
- Test temperature: 20 - 25°C (room temperature)
- Continuous darkness: no, indirect daylight.
- Estimation Technique : TOC/DOC Analyzer 500TEST SYSTEM
- Number of culture flasks/concentration: 2 tests running in parallel - Reference substance:
- diethylene glycol
- Key result
- Parameter:
- % degradation (DOC removal)
- Value:
- ca. 1
- Sampling time:
- 28 d
- Details on results:
- Adsorption: The adsorption of the test substance after 3 hours was 12 %.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- not inherently biodegradable
- Conclusions:
- The biodegradation of the test substance after 28 days was: 1 %
- Executive summary:
The inherent biodegradability of test substance was determined in a Zahn-Wellens / EMPA test, performed according to the OECD Guideline for Testing of Chemicals, No. 302B, 1992. The test substance and the reference substance Diethylenglycol, respectively, were tested in concentrations of 150 mg/l DOC.
Results
Adsorption: The adsorption of the test substance after 3 hours was: 12 %
Biodegradation: The biodegradation of the test substance after 28 days was: 1 %
The total elimination of the test substance after 28 days was: 12 %
The biodegradation of the reference substance after 7 days was: 100 %
- Endpoint:
- biodegradation in water: screening test, other
- Remarks:
- BOD5/COD evaluation
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- September 23, 1975
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
- Qualifier:
- according to guideline
- Guideline:
- other: Internal method 15
- Qualifier:
- according to guideline
- Guideline:
- other: Internal method 16
- Principles of method if other than guideline:
- The biological oxygen demand BOD is the amount of oxygen needed to degrade organic substances present in waste water with the help of bacteria (and other microorganisms present in sludge). The expression BOD5 represents the oxygen consumption within 5 days of incubation at 20 °C. Various dilutions of a substance solution in oxygen saturated water will be measured for its oxygen content before and after such an incubation period. Within this procedure chemical oxygen demand (COD) is defined as the equivalent amount of oxygen in terms of amount of potassium dichromate that is consumed by reacting with the oxidizable components of 1 g of sample material dissolved in 1 liter water under the given reaction conditions.
- GLP compliance:
- no
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- not specified
- Duration of test (contact time):
- ca. 21 d
- Initial conc.:
- ca. 500 mg/L
- Based on:
- test mat.
- Initial conc.:
- ca. 10 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Remarks on result:
- not determinable because of methodological limitations
- Key result
- Parameter:
- BOD5
- Value:
- ca. 0 mg O2/g test mat.
- Key result
- Parameter:
- COD
- Value:
- ca. 792 mg O2/g test mat.
- Key result
- Parameter:
- BOD5*100/COD
- Value:
- ca. 0 mg O2/g test mat.
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- BOD5 = 0 mg/g O2
COD = 972 mg/g O2
BOD5/COD = 0 - Executive summary:
The substance has been tested for biodegradation according to the Ciba Geigy AG internal method 15 and 16.
The substance shows the following results:
BOD5 = 0 mg/g O2
COD = 972 mg/g O2
BOD5/COD = 0
Referenceopen allclose all
The biodegradation of the reference substance, corrected by the blank control and measured as DOC (mg/l) is: 100 % 7th day (average of 2 tests running in parallel).
Biochemical oxygen demand or BOD is the amount of dissolved oxygen needed by aerobic biological organisms in a body of water to break down organic material present in a given water sample at certain temperature over a specific time period. The term also refers to a chemical procedure for determining this amount. This is not a precise quantitative test, although it is widely used as an indication of the organic quality of water, therefore is not be used as quantitative date about ready biodegradation.
Description of key information
The substance is nor ready nor inherent biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
Additional information
The substance has been tested by one screening study (BOD5, COD) and one study of inherently biodegradation.
The screening test has been conducted in 1975 according to the CIBA GEIGY AG internal method 15 and 16. The purity of substance is approx. 85 %.
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 their ratio 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.).
As indicated in the ECHA Guidance R.7b, the BOD5 test is a traditional biodegradation test that is now replaced by the ready biodegradability tests. Therefore, this test should not be performed today for assessment of the ready biodegradability of substances.
Older test data may, however, be used when no other degradability data are available.
For the assessment it is only available a summary on BOD5 and COD.
COD was measured according to Method A-16. The COD measured was 792 mg/g O2, at concentration of 500 mg/l.
BOD5 was measured according to Method A-15. The BOD5 measured was 0 mg/g O2, at concentration of 10 mg/l.
The ratio BOD5/COD is 0.
When the ratio BOD5/COD > 0.5 the situation can be compared with short time period degradation (readily biodegradable), but it is not our case.
No more data are available, therefore no other discussion can be made.
Inherent biodegradation
This evaluation is supported by the study of inherent biodegradation conducted according the guideline OECD 302B. The purity of substance is 90 %. After 28 days of test period, the biodegradation observed was 1 %.
Based on data in our possess, the substance is not ready biodegradable as shown on 5 days screening study and not inherently biodegradable on basis of the result of inherently biodegradation study after 28 days according to the OECD 302B.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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