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EC number: 202-815-9 | CAS number: 100-06-1
- 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: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992-02-18 to 1992-03-17
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- no replicate was performed or recorded.
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.4-B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test)
- Deviations:
- yes
- Remarks:
- Tox-control not performed
- GLP compliance:
- yes
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum: activated sludge, derived from the effluent of a laboratory-scale activated sludge plant receiving domestic sewage (Wupperverband)
- Test organisms: mixed culture of microorganisms
- Concentration of sludge: 0.5 mL / 900 mL
- Pretreatment: no
- sampling date: 02/18/1992 - Duration of test (contact time):
- 28 d
- Initial conc.:
- 20 mg/L
- Based on:
- DOC
- Parameter followed for biodegradation estimation:
- DOC removal
- Details on study design:
- TEST CONDITIONS
- Composition of medium: according to OECD Guideline 301 E
- Test temperature: 20-24 °C
- Continuous darkness: yes
SAMPLING
- Sampling frequency: sampling on days 7, 14, 21, 27 and 28
CONTROL AND BLANK SYSTEM
- Toxicity control: not performed
- procedure control: yes, with reference substance aniline
- Reference substance:
- aniline
- Preliminary study:
- Not performed
- Test performance:
- All validity criteria were fulfilled. The test item reached the 10 % level after 7 days and passed the level > 70 % after 14 days as a biodegradation rate of 100 % was already reached.
- Key result
- Parameter:
- % degradation (DOC removal)
- Value:
- 100
- Sampling time:
- 28 d
- Results with reference substance:
- The reference substance in parallel procedure control was ready degraded (100%) within 28 days.
- Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The ready biodegradability of the test item was determined with a non-adapted activated sludge over a test period of 28 days in the Modified OECD Screening Test according to the OECD guideline 301 E and the EU Method C.4 -B. The test item is classified as readily biodegradable as the pass level of 70 % degradation was reached in a 10-d-window within the 28 days period of the study.
- Executive summary:
The ready biodegradability of the test substance was investigated according to EU Method C.4 -B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test) and GLP principles. The biodegradation of the test substance was followed by exposing it to microorganisms from the effluent of a laboratory-scale activated sludge plant (receiving domestic sewage). As a reference compound (procedure control) aniline was tested simultaneously. The test item concentration selected as appropriate was 20 mg/L DOC. The flasks were incubated for 28 days under aerobic and dark conditions at 20-24 °C. The biodegradability was derived from DOC removal within the test period. In result, the test item reached the 10 % level after 7 days and passed the level >70 % after 14 days as a biodegradation rate of 100 % was already reached. All validity criteria were fulfilled. In conclusion, the test item is regarded to be in the 10-d-window and after 28 days readily biodegradable.
Reference
Table: DOC values [mg/L] for the blank control and the test item as well as degradation [%] of the test item after 0, 7, 14, 21 and 28 days.
Time | Blank | Test Item | ||
DOC (mg/l) |
DOC (mg/l) | DOC cor. (mg/l) | Degradation (%) | |
0 h | 2 | 19 | 17 | 0 |
7 d | 2 | 17 | 15 | 12 |
14 d | 2 | 0 | 0 | 100 |
21 d | 2 | 0 | 0 | 100 |
28 d | 2 | 0 | 0 | 100 |
Description of key information
The test item reached a biodegradation rate of 100 % after 14 days. The test item is regarded to be in the 10-d-window and after 28 days readily biodegradable.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
A 28-day biodegradation study was carried out for the test substance according to EU Method C.4 -B (Determination of the "Ready" Biodegradability - Modified OECD Screening Test) and GLP principles. Test solutions were inoculated with activated sludge and incubated under aerobic conditions for 28 days. The DOC-value of the stock solution of the test item was 144 mg/L and the test temperature was in the range of 20 to 24 °C. A procedure control with the reference substance aniline was performed in parallel. The test substance was found to be 100 % degraded after 14 days. The 10-day window was met. Thus, the test substance is considered to be readily biodegradable. The reference substance was completely biodegraded (100%) after 28 days. All validity criteria of the guidelines were met.
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