Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 202-700-3 | CAS number: 98-79-3
- 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: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 08 November to 09 December 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 F (Ready Biodegradability: Manometric Respirometry Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and batch No.of test material: 20140124
- Expiration date of the lot/batch: No data
- Purity test date: No data
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Ambient temperature
- Stability under test conditions: No data - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge, domestic, non-adapted
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure): Collected from aeration tank 2 of 'STEP de Lille", 33290 Blanquefort, France water treatment plant
- Preparation of inoculum for exposure: Filtered through 1mm sieve to remove coarse particles, sludge washed by decanting in mineral medium until sludge was considered free from excess subtrate or inhibitor
- Pretreatment: Pre-conditioning consisted of aerating sludge in mineral medium for 5-7 days at test temperature
- Concentration of sludge: 3.65 g/L suspended solid
- Initial cell/biomass concentration:
- Water filtered: No - Duration of test (contact time):
- >= 28 d
- Initial conc.:
- >= 100 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Composition of medium: As described in guideline, medium was prepared from concentrated stock in ultrapure water (Na2HPO4.2H2O 334 mg/L, K2HPO4 217.5 mg/L, KH2PO4 85 mg/L, NH4Cl 5 mg/L, CaCl2.2H2O 36.4 mg/L, MgSO4.7H2O 22.5 mg/L, FeCl3.6H2O 0.25 mg/L)
- Test temperature: 20-24oC (actual range 21.9 - 22.4oC)
- pH: Day 0 6.4 - 7.6; Day 28 6.3 - 7.3
- pH adjusted: yes/no
- CEC (meq/100 g):
- Aeration of dilution water:
- Suspended solids concentration: final concentration approximately 30 mg/L
- Continuous darkness: Yes
- Other:
TEST SYSTEM
- Culturing apparatus:
- Number of culture flasks/concentration:
- Method used to create aerobic conditions:
- Method used to create anaerobic conditions:
- Measuring equipment:
- Test performed in closed vessels due to significant volatility of test substance:
- Test performed in open system:
- Details of trap for CO2 and volatile organics if used:
- Other:
SAMPLING
- Sampling frequency:
- Sampling method:
- Sterility check if applicable:
- Sample storage before analysis:
- Other:
CONTROL AND BLANK SYSTEM
- Inoculum blank:
- Abiotic sterile control:
- Toxicity control:
- Other:
STATISTICAL METHODS: - Reference substance:
- benzoic acid, sodium salt
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 100.7
- Sampling time:
- 7 d
- Remarks on result:
- other: ThOD NH4 (1.115 mg O2/mg/test substance)
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 69.7
- Sampling time:
- 7 d
- Remarks on result:
- other: ThOD NO3 (1.611 mg O2/mg test substance)
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 112.4
- Sampling time:
- 14 d
- Remarks on result:
- other: ThOD NH4 (1.115 mg O2/mg test substance)
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 77.8
- Sampling time:
- 14 d
- Remarks on result:
- other: ThOD NO3 (1.611 mgO2/mg test substance)
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 114.1
- Sampling time:
- 21 d
- Remarks on result:
- other: ThOD NH4 (1.115 mg O2/mg test substance)
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 79
- Sampling time:
- 21 d
- Remarks on result:
- other: ThOD NO3 (1.611 mgO2/mg test substance)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 114
- Sampling time:
- 28 d
- Remarks on result:
- other: ThOD NH4 (1.115 mg O2/mg test substance)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- >= 78.9
- Sampling time:
- 28 d
- Remarks on result:
- other: ThOD NO3 (1.611 mgO2/mg test substance)
- Details on results:
- Start of 10-day window was Day 2, and at the end of the 10-day window the degradation was 71.2% (Day 5, ThOD NH4) and 60.9% (Day 6, ThOD NO3)
- Results with reference substance:
- The positive control showed 80.8% degradation after 14 days and 79.3% degradation after 28 days
The toxicity control showed 104.5% degradation after 14 days and 105.1% degradation after 28 days - Validity criteria fulfilled:
- yes
- Interpretation of results:
- readily biodegradable
- Conclusions:
- The test substance was readily biodegradable under the conditions of the test
- Executive summary:
A study was performed to assess the ready biodegradability of the test substance according to OECD test guideline OECD 301F (Determination of ready biodegradability - manometric respiration test), in compliance with GLP.
The test substance, at nominal 100 mg/L in mineral medium, was inoculated with effluent from a treatment works treating predominantly domestic sewage and incubated for 28 days. During this period the biodegradation was followed by O2 consumption, based on the ThOD of the test substance. The ThOD defined as the total amount of oxygen required to oxidise the test substance completely; and was calculated assuming no nitrification occurs (ThOD NH4) and assuming nitrification occurs (ThOD NO3).
The test substance showed 100.7, 112.4, 114.1 and 114.0% degradation after 7, 14, 21 and 28 days (assuming no nitrification occurs) and 68.7, 77.8, 79.0 and 78.9% degradation after 7, 14, 21 and 28 days (assuming nitrification occurs).
The positive control showed 80.8% degradation after 14 days and 79.3% degradation after 28 days.
The toxicity control showed 104.5% degradation after 14 days and 105.1% degradation after 28 days.
The test substance is considered to be readily biodegradable under the conditions of the test and is not considered to have an inhibitory effect on sewage treatment process microorganisms at the nominal test concentration of 100 mg/L.
The study is considered acceptable and satisfies the guideline requirements for a biodegradation in water screening test.
Reference
Day |
% degradation |
||||
Test substance1 |
Test substance2 |
Positive control |
Toxicity control |
Abiotic control |
|
7 |
100.7 |
69.7 |
73.3 |
95.8 |
- |
14 |
112.4 |
77.8 |
80.8 |
104.5 |
- |
21 |
114.1 |
79.0 |
80.6 |
105.1 |
- |
28 |
114.0 |
78.9 |
79.3 |
105.1 |
0 |
1 ThOD NH4= 1.115 mgO2/mg test substance
2 ThOD NO3= 1.611 mgO2/mg test substance
Description of key information
A reliable study was performed to assess the ready biodegradability of the test substance according to the test guideline OECD 301F (Determination of ready biodegradability - manometric respiration test), in compliance with GLP.
The test substance was incubated with mineral medium and effluent from a treatment works treating predominantly domestic sewage for 28 days. Biodegradation was based on O2 consumption and the ThOD of the test substance. The ThOD, defined as the total amount of oxygen required to oxidise the test substance completely; was calculated assuming no nitrification occurs (ThOD NH4) and nitrification occurs (ThOD NO3).
The test substance showed 114% degradation after 28 days (assuming no nitrification occurs) and 79% degradation after 28 days (assuming nitrification occurs).
The test substance is considered to be readily biodegradable and meets the 10 -day window criterion under the conditions of the test.
The study is considered acceptable and satisfies the guideline requirements for a biodegradation in water screening test.
Key value for chemical safety assessment
- Biodegradation in water:
- readily biodegradable
Additional information
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.