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: 911-436-4 | CAS number: 61932-63-6
- 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

Endpoint summary
Administrative data
Description of key information
Fish
PR022
In a reliable 96-hours acute toxicity study on Oryzias latipes performed according to OECD 203 and compliant to GLP (reliability category 1), the test item caused neither lethality nor abnormal behaviour or mobility at the applied limit concentration of nominal 100 mg/L (geometric mean measured concentration: 100 mg/L). Also no lethality nor abnormal behaviour or mobility was observed in the control and the solvent control (containing the amount of HCO-40 used in the treatment group). The following (no)effect concentrations were determined (geometric mean measured concentrations): LC50 (96 h): > 100 mg/L; LC0 (96 h): 100 mg/L; EC0 (96 h, behaviour & mobility): 100 mg/L.
Aquatic Invertebrates
PR022
In a reliable 48-hours acute toxicity study on Daphnia magna performed according to OECD 202 and compliant to GLP (reliability category 1), the test item caused no immobilization at the applied limit concentration of nominal 100 mg/L (geometric mean measured concentration: 110 mg/L). No immobilization occured in the control and the solvent control (containing the amount of HCO-40 used in the treatment group). The following (no)effect concentrations were determined (geometric mean measured concentrations): EC50 (48 h): > 110 mg/L; LOEC (48 h): > 110 mg/L; NOEC (48 h): 110 mg/L
PR022
In a daphnia magna reproduction test performed according to OECD 211 and compliant to GLP (reliability category 1) with semistatic test design (test medium renewal every 48 hours) no statistically significant effects were observed at the limit test item concentration of 30 mg/L (time weighted mean measured concentration). The following (no)effect concentrations (21 days) were determined:
LC50 (adult mortality) > 30 mg/L (TWA)
LOEC (reproduction, adult mortality, macroscopic effects) > 30 mg/L (TWA)
NOEC (reproduction, adult mortality, macroscopic effects) = 30 mg/L (TWA)
The validity criteria of the guideline were met.
PR112
The test substance was tested in a daphnia magna reproduction test performed according to OECD 211 and compliant to GLP (reliability category 1). At the saturated solution of the test item with a nominal loading of 1.00 mg/L no biologically or statistically significant effects were determined. The No Observed Effect Loading (NOEL) and the Lowest Observed Effect Loading (LOEL) were assessed at:
NOEL: Saturated Solution (with the nominal loading of 1.00 mg/L)
LOEL: > Saturated Solution (with the nominal loading of 1.00 mg/L)
All effect values given are based on the saturated solution of the test item with the nominal loading of 1.00 mg/L.
Algae
PR210
In this study no inhibition on growth of the freshwater green alga Desmodesmus subspicatus was found after 72 hours exposure to the test item. The NOEC for inhibition of specific growth rate and yield after 72 hours was 1.00 mg/L.
The test item caused a slight stimulation of the algae growth. All effect levels are given based on the nominal concentration of the test item.
Microorganisms
PR112
A Respiration Inhibition Test with activated sludge according to OECD Guideline No. 209 was performed compliant to GLP with the submission substance (reliability category 1). TThe test was performed under static conditions with the nominal limit concentration of 1000 mg/L. The respiration rates of control, reference and test item concentrations were measured after a contact time of three hours, and the inhibitory effects of the test and reference concentrations were determined in comparison to the control respiration rates. No inhibition was observed at the tested limit concentration.
Validity criteria of the test guideline were fulfilled.
The test item is not toxic at concentrations >= 1000 mg/L to activated sludge of a municipal sewage treatment plant.
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.
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.
