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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 485-350-6 | CAS number: 405095-33-2
- 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:
- July - August 1992
- 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:
- yes
- Remarks:
- In deviation from the Guideline settled sludge instead of centrifugated sludge was used.
- GLP compliance:
- yes
- Remarks:
- This study has been performed in compliance with GLP in Switzerland, Procedures and Principles, March 1986, issued by the Swiss federal Department of the Interior and the Intercantonal Office for the Control of Medicaments.
- Analytical monitoring:
- not required
- Vehicle:
- no
- Test organisms (species):
- activated sludge
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 3 h
- Key result
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- 64.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 3 h
- Dose descriptor:
- other: EC20
- Effect conc.:
- 7.3 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Duration:
- 3 h
- Dose descriptor:
- EC100
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of total respiration
- Remarks:
- respiration rate
- Validity criteria fulfilled:
- yes
- Remarks:
- The two control respiration rates are within 15 % of each other and the EC50 (3h) of 3,5-Dichlorphenol is in the accepted range 5 to 30 mg/l
- Conclusions:
- EC50 (3h) = 64.2 mg/L
EC20 (3h) = 7.3 mg/L
EC100 (3h) > 100 mg/L - Executive summary:
The toxicity of CA 1139 A to activated sludge was determined in a 3-hours respiration inhibition test, according to GLP Guideline OECD 209, under aerobic conditions at room temperature (20 +/-2 ºC). The experiment was conducted in compliance with Good Laboratory Practice (GLP) in, Procedures and Principles, March 1986, issued by the Federal Department of the interior and the Intercantonal Office for the Control of Medicaments.
The test substance concentrations tested were 100.3, 32.1, 10.0, 3.2 and 1.0 mg/l. The reference substance 3,5-Dichlorophenol was tested in concentrations of 32, 10 and 3.2 mg/l.
The test system consisted of activated sludge collected from a communal sewage treatment plant. 1.69 g/l sludge (dry weight) was used.
The respiration rate of the activated sludge fed with a standard amount of synthetic sewage feed was measured (ORION – Electrode Type 97-08, ORION Microprocessor Ionalizer 901) after a contact time of 3 hours with the test substance. The reference substance 3,5-Dichlorophenol and a blank (synthetic sewage feed, inoculum and water) served as controls.
The following values have been graphically determined:
EC50 (3h) = 64.2 mg/L
EC20 (3h) = 7.3 mg/L
EC100 (3h) > 100 mg/L
The results are based on nominal concentrations.
Reference
Description of key information
The toxicity of CA 1139 A to activated sludge was determined in a 3-hours respiration inhibition test,
according to GLP Guideline OECD 209, under aerobic conditions at room
temperature (20 +/-2 ºC). The experiment was conducted in compliance
with Good Laboratory Practice (GLP) in, Procedures and Principles, March
1986, issued by the Federal Department of the interior and the
Intercantonal Office for the Control of Medicaments.
The test substance concentrations tested were 100.3, 32.1, 10.0, 3.2 and
1.0 mg/l. The reference substance 3,5-Dichlorophenol was tested in
concentrations of 32, 10 and 3.2 mg/l.
The test system consisted of activated sludge collected from a communal
sewage treatment plant. 1.69 g/l sludge (dry weight) was used.
The respiration rate of the activated sludge fed with a standard amount
of synthetic sewage feed was measured (ORION – Electrode Type 97-08,
ORION Microprocessor Ionalizer 901) after a contact time of 3 hours with
the test substance. The reference substance 3,5-Dichlorophenol and a
blank (synthetic sewage feed, inoculum and water) served as controls.
The following values have been graphically determined:
EC50 (3h) = 64.2 mg/L
EC20 (3h) = 7.3 mg/L
EC100 (3h) > 100 mg/L
The results are based on nominal concentrations.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 64.2 mg/L
Additional information
Guideline Test Type |
Species |
Results |
Reference |
Reliability |
OECD 209 |
activated sludge of a communal sewage treatment plant |
EC50(3h) = 64.2 mg/l EC20(3h) = 7.3 mg/L EC100(3h) > 100 mg/L
|
Ciba-Geigy Ltd., Baumann, W.; 1992 |
Reliable without restriction |
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.