Registration Dossier
Registration Dossier
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: 223-798-4 | CAS number: 4078-19-7
- 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

Short-term toxicity to fish
Administrative data
Link to relevant study record(s)
Description of key information
In a static non GLP short-term toxicity to fish test (BASF SE, 10F0680/895245, 1990) according to DIN 38412 – L15 guideline (equivalent to OECD 203), the 96-hour LC50 of the test substance for Leusciscus idus (Golden Orfe) was determined to be nominal in the range of 100 - 215 mg/L.
Key value for chemical safety assessment
Additional information
The acute toxicity of the test substance to fish Leusciscus idus (Golden Orfe) was determined in a study (BASF SE, 10F0680/895245, 1990) according to DIN 38412 – L15 (1982) guideline (equivalent to OECD 203) under non GLP conditions. In this static short-term toxicity to fish test the test substance was tested in the nominal concentrations of 0 (control), 46.4, 100, 215, 464 and 1000 mg/L. No concentrations of the test substance were measured. This study encompassed one treatment group for the dose rates of the test item and one replicate for the control. Each group contained 10 individuals. A positive control with the reference substance chloroacetamide was used. The test fish were observed after 1, 4, 24, 48, 72 and 96 hours test duration for sublethaI effects and mortality. The water quality parameters (pH, temperature and oxygen content) were determined after 1, 24, 48, 42 and 96 hours. The water pH, temperature and dissolved oxygen were within acceptable guideline specifications. There were no toxic effects observed in any treatment group during this test. The LC50 of the reference substance was determined to be 34 mg/L after 48 hours. All validity criteria were met. The 96h-LC50 of the test substance was determined to be nominal in the range of 100 – 215 mg/L.
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.
