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EC number: 212-667-7 | CAS number: 841-77-0
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2016-01-27 to 2016-03-11
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test (Carbon and Ammonium Oxidation))
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- ISO 8192 (Water quality - Test for inhibition of oxygen consumption by activated sludge for carbonaceous and ammonium oxidation)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.11 (Biodegradation: Activated Sludge Respiration Inhibition Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: M15BB1451
- Expiry date: 2021-01-30
- Purity test date: 2015-05-21 (date of certificate of analysis)
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- storage conditions: room temperature
- Stability under test conditions: until expiry date (2021-01-30)
- Solubility and stability of the test substance in the solvent/vehicle: solubility in water: not indicated
OTHER SPECIFICS:
- CAS n°: 841-77-0
- Solubility in water: 0.45 g/L
- Analytical purity: Assay Base Titration 98.8%
- Impurities (identity and concentrations): HPLC purity: R095795 <0.1%, R00350 <0.1%, R052209 <0.1%, R053616 <0.1%, R048205 <0.1%, sum of other impurities except R095795, R00350 <0.05% - Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: The test item was not sufficiently soluble to allow the preparation of a 10 g/L stock solution in water. 1-Litre test bottles were filled with 200 mL of test item mixtures in Milli-RO water (tap-water purified by reverse osmosis; Millipore Corp., Bedford, Mass., USA) with initial loading rates of 2.5 times the final loading rate. These mixtures were stirred in closed dark brown bottles for approximately 24 hours. Subsequently, 16 mL synthetic medium made up to 50 mL with Milli-RO water and 250 mL sludge were added resulting in the required loading rates. Optimal contact between the test item and test organisms was ensured applying continuous aeration and stirring.
- Controls: blank controls: test medium without test item and treated in the same way as the test item solutions. - Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Laboratory culture: predominantly domestic sewage treatment plant, "Waterschap Aa en Maas", 's-Hertogenbosch, The Netherlands.
- Preparation of inoculum for exposure: coarsely sieved (1 mm) and allowed to settle. The supernatant was removed and ISO-medium was added. A small amount of the sludge was weighed and dried overnight at ~105°C to determine the amount of suspended solids
- Pretreatment: The batch of sludge was used one day after collection; therefore 50 mL of synthetic medium was added per L of activated sludge at the end of the collection day. The sludge was kept aerated at test temperature until use.
- Initial biomass concentration: 3.0 g/L of sludge - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Test temperature:
- between 18 and 20°C (complied with the requirements as laid down in the study plan (20 ± 2°C))
- pH:
- at start between 7.6 and 8.2.
After the 3 hours between 7.3 and 8.1. - Dissolved oxygen:
- DO concentration at the start was above 60-70% saturation (60% of air saturation is > 5 mg/L at 20°C) and to maintain the sludge flocs in suspension.
- Nominal and measured concentrations:
- Nominal concentrations:
- combined limit/range-finding test: 10, 100 and 1000 mg/L
- final test: 4.6, 10, 22, 46 and 100 mg/L.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: All glass
- Type (delete if not applicable): open
- Aeration: adjusted such that the dissolved oxygen concentration at the start was above 60-70% saturation (60% of air saturation is > 5 mg/L at 20°C) and to maintain the sludge flocs in suspension.
- No. of vessels per concentration (replicates): 5 (final test)
- No. of vessels per control (replicates): 5
- Sludge concentration (weight of dry solids per volume): initial loading ca. 3.0 g dw/L
- Nutrients provided for bacteria: no
- Nitrification inhibitor used (delete if not applicable): none
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Tap-water purified by reverse osmosis (Millipore Corp., Bedford, Mass., USA).
* CaCl2.2H2O 211.5 mg/L
* MgSO4.7H2O 88.8 mg/L
* NaHCO3 46.7 mg/L
* KCl 4.2 mg/L
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): Determination of oxygen was performed with multiple oxygen probes connected to a BlueBox (GO-Systemelektronik GmbH, Germany), a multichannel measuring and controlling system.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.2
- Range finding study: 10, 100 and 1000 mg/L
- Test concentrations: 4.6, 10, 22, 46 and 100 mg/L.
- Results used to determine the conditions for the definitive study: yes - Reference substance (positive control):
- yes
- Remarks:
- 3,5-Dichlorophenol
- Key result
- Duration:
- 3 h
- Dose descriptor:
- other: NOELR
- Effect conc.:
- 22 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Key result
- Duration:
- 3 h
- Dose descriptor:
- other: ELR10
- Effect conc.:
- 29 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks on result:
- other: 95% CL: 10-41 mg/L
- Key result
- Duration:
- 3 h
- Dose descriptor:
- other: ELR50
- Effect conc.:
- 70 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks on result:
- other: 95% CL: 54-96 mg/L
- Details on results:
- - Blank controls oxygen uptake rate: 51 mg O2/L.h
- Coefficient of variation of oxygen uptake rate in control replicates: 4 - Results with reference substance (positive control):
- 3-h EC50 = 7.326 and 4.718 mg/L (for the range-finding and limit test respectively).
This is within the recommended range of 2-25 mg/L confirming suitability of the activated sludge used. - Reported statistics and error estimates:
- The 3-h EC50 values were based on Probit Analysis.
The NOEC determination was based on the Welch-t test for inhomogeneous variances with Bonferroni-Holm Adjustment, alpha=0.05, one sided, smaller. - Validity criteria fulfilled:
- yes
- Conclusions:
- Under the conditions of this present test JNJ-130806-AAA (T000750) was not toxic to waste water bacteria (activated sludge) at or below a loading rate of 22 mg/L (NOELR).
The ELR10 was at a loading rate of 29 mg/L (95% confidence limits 10-41). The ELR50 was at a loading rate of 70 mg/L (95% confidence limits 54-96).
These results can be considered reliable without restriction.
Reference
Description of key information
The study of 2016, investigating the acute toxicity of T000750 to microorganisms according to OECD guideline 209, was considered as the key study for endpoint coverage. The 3-h ELR50 was 70 mg/L.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 70 mg/L
- EC10 or NOEC for microorganisms:
- 22 mg/L
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.
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