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EC number: 231-272-0 | CAS number: 7473-98-5
- 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
- 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
- Deviations:
- not specified
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- activated sludge, domestic
- Details on inoculum:
- - Method of cultivation: Activated sludge from the municipal wastewater treatment plant of Mannheim, Germany was collected on 23 Feb 2010 from the aeration tank of the plant
- Preparation of inoculum for exposure: The sludge suspension was sieved with a fine woven mesh (mesh size about 1mm).
- Pretreatment: The suspension was pre-aerated over night at room temperature. At thenext day the sludge suspension was washed with tap water once. After that the suspension was adjusted to 7.5 g/L dry matter
- Initial biomass concentration: 1.5 g/L dry matter - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 180 min
- pH:
- 7.2 at test start
7.9 - 8.0 at the end of the exposure - Nominal and measured concentrations:
- nominal: blank, 62.4, 125, 250, 500 and 1000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 250 ml Erlenmeyer-vessels
- Material, size, headspace, fill volume: glass, fill volume = 250 mL
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
- Biomass loading rate: 1.5 g/L dry matter
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: 8 mL/vessel 100-fold concentrated OECD medium
OTHER TEST CONDITIONS
- Adjustment of pH: no
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : oxygen consumption
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2 - Reference substance (positive control):
- yes
- Remarks:
- 3,5 dichlorophenol
- Duration:
- 180 min
- Dose descriptor:
- EC10
- Effect conc.:
- 450 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 180 min
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 180 min
- Dose descriptor:
- other: EC20
- Effect conc.:
- 600 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Results with reference substance (positive control):
- - Results with reference substance valid? yes
- Relevant effect levels: EC50 = 8.0 mg/L - Reported statistics and error estimates:
- The values were given with an accuracy of 2 significant digits. The degree of inhibition was evaluated by Probit analysis according to Finney
- Validity criteria fulfilled:
- yes
- Conclusions:
- The inhibition of the degradation activity of activated sludge is not anticipated when introduced to biological treatment plants in appropriate low concentrations.
- Executive summary:
In this guideline (OECD 209) study with GLP certification, the 3 hour EC50 of the test material to sewerage microorganisms was determined to be >1000 mg/l (nominal). The test was conducted upon a washed activated sewerage sludge taken from a municipal sewerage treatment plant. The test material is not expected to inhibit sewerage microorganisms at low concentrations.
Reference
Assay identification |
BC1 |
BC2 |
RS1 |
RS2 |
RS3 |
TS1 |
TS2 |
TS3 |
TS4 |
TS5 |
O2 concentration Start [mg/L] |
7.4 |
7.0 |
7.4 |
8.5 |
8.8 |
8.3 |
7.7 |
7.6 |
7.7 |
7.1 |
O2 concentration after 6 minutes [mg/L] |
6.0 |
5.5 |
6.0 |
8.0 |
8.7 |
7.5 |
6.5 |
6.0 |
6.0 |
5.0 |
O2 consumption rate [mg/L in 6 min] |
1.4 |
1.5 |
1.4 |
0.5 |
0.1 |
0.8 |
1.2 |
1.6 |
1.7 |
2.1 |
O2 consumption rate [mg/L*h] |
14 |
15 |
14 |
5 |
1 |
8 |
12 |
16 |
17 |
21 |
Specific O2 consumption rate [mg O2/g*h] |
9 |
10 |
9 |
3 |
1 |
5 |
8 |
11 |
11 |
14 |
RS/TS concentrations [mg/L] |
- |
1 |
10 |
100 |
1000 |
500 |
250 |
125 |
62.4 |
|
Calculation of inhibition respiration [%] |
- |
- |
3 |
66 |
93 |
45 |
17 |
-10 |
-17 |
-45 |
Legend: TS = test item, RS = reference item, BC = blank control
Description of key information
Study conducted to recognised training guidelines with GLP certification.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 mg/L
- EC10 or NOEC for microorganisms:
- 450 mg/L
Additional information
In the key study on the toxicity of the test substance on activated sludge an EC10 of 450 mg/L and an EC50 of > 1000 mg/L was reported. The test was conducted under GLP regulations and according to OECD test guideline 209. The respiration inhibition was determined in activated sludge obtained from a municipal sewage treatment plant. The effect concentrations were derived after a test duration of 3 hours.
A supporting study was conducted using the test material before the final distillation and industrial activated sludge. The EC50 after 30 min was determined to be 3 mg/L. However, the value will not be used in the risk assessment since test material without the final distillation was used and a more reliable up-to-date key study is available.
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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