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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 701-196-7 | CAS number: -
- 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:
- 14 -15 April 2010
- 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
- Version / remarks:
- (1984)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- not required
- Vehicle:
- no
- Details on test solutions:
- The test substance was directly weighed out in each test vessel. After 24h of stirring the test substance was completely dispersed.
- Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Origin: Municipal sewage treatment plant of D-31157, Sarstedt Germany
- Preparation of inoculum for exposure:
- Pretreatment: The sludge was washed twice with autoclaved tap water and adjusted corresponding to a dry weight of 4.0 g/L ± 10%. The sludge was used within 24 h after sampling.
- Dry sludge concentration: 3.97 g/L - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Hardness:
- Not reported
- Test temperature:
- 20.9 °C
- pH:
- 6.89
- Dissolved oxygen:
- 5.2 - 7.7 mg O2/L (determined at the start of the measurement)
- Nominal and measured concentrations:
- Nominal concentrations: 0 (control), 100, 180, 320, 580 and 1000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 500 mL Erlenmeyer flasks
- Aeration: Permanent
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 2
TEST MEDIUM / WATER PARAMETERS
Composition of the test medium:
200 mL inoculum
16 mL synthetic waste water
284 mL autoclaved tap water
test item concentration (directly weighed out in each test vessel)
EFFECT PARAMETERS MEASURED:
The oxygen depletion of the control, reference and test item replicates was measured after 3 hours incubation by means of an oximeter and recorded for at least 3 minutes on a flat bed recorder.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.8
- Range finding study: Yes
- Test concentrations: 0 (control), 10, 100 and 1000 mg/L
- Results used to determine the conditions for the definitive study: 0% inhibition at 10 mg/L, 4% inhibtion at 100 mg/L and 18% at 1000 mg/L - Reference substance (positive control):
- yes
- Remarks:
- copper (II) sulphate pentahydrate
- Key result
- Duration:
- 3 h
- 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
- Details on results:
- The EC10 is estimated by the reviewer to be 1000 g/L (11% inhibition at 1000 mg/L and 9% inhibition at 580 mg/L).
- Results with reference substance (positive control):
- The 3h-EC50 of the refence substance copper (II) sulphate pentahydrate was 103 mg/L which is within the recommended confidence range of 54 - 156 mg/L
- Validity criteria fulfilled:
- yes
- Remarks:
- The two control respiration rates differ not more than 15% in the study. The 3h-EC50 of copper (II) sulphate pentahydrate is within the accepted range of 54-156 mg/L.
- Conclusions:
- The 3h-EC50 of the test substance to activated sludge was > 1000 mg/L
The 3h-EC10 of the test substance to activated sludge, estimated by the reviewer was 1000 mg/L - Executive summary:
The toxicity of the test substance to activated sludge was investigated according to OECD guideline 209 and GLP.
The 3h-EC50 of the test substance to activated sludge was > 1000 mg/L
The 3h-EC10 of the test substance to activated sludge, estimated by the reviewer (based on 11% inhibition at 1000 mg/L and 9 % inhibition at 580 mg/L) was ca. 1000 mg/L.
Because the test was carried out according to OECD209 and GLP an no shortcomings were observed a reliability 1 was assigned.
Reference
Table: Respiration rates and inhibition of respiration of test and reference item concentrations.
Treatment |
Concentration (mg/L) |
Respiration rate (mg O2/L/h) |
Inhibition (%) |
Test item |
1000 |
28.0 |
11 |
580 |
28.8 |
9 |
|
320 |
31.6 |
0 |
|
180 |
30.0 |
5 |
|
100 |
32.8 |
-4 |
|
Control |
- |
31.2 |
- |
- |
32.0 |
- |
|
Reference item |
180 |
9.2 |
71 |
100 |
14.8 |
53 |
|
58 |
23.6 |
25 |
Description of key information
The 3h-EC50 of the test substance to activated sludge was > 1000 mg/L.
The 3h-EC10 of the test substance to activated sludge, estimated by the reviewer was 1000 mg/L.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 mg/L
Additional information
The toxicity of the test substance to activated sludge was investigated according to OECD guideline 209 and GLP.
The 3h-EC50 of the test substance to activated sludge was > 1000 mg/L.
The 3h-EC10 of the test substance to activated sludge, estimated by the reviewer (based on 11% inhibition at 1000 mg/L and 9 % inhibition at 580 mg/L) was ca. 1000 mg/L. Based on the fact that this is an estimation, the worst-case EC50 value of 1000 mg/L is taken as key value for the CSA.
Since the test was carried out according to OECD209 and GLP, and because no shortcomings were observed a reliability 1 was assigned.
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.