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Diss Factsheets
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EC number: 201-291-9 | CAS number: 80-56-8
- 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:
- toxicity to microorganisms, other
- Remarks:
- Ready biodegradability test according to OECD 301 D used to derive PNEC microorganisms.
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Reason / purpose for cross-reference:
- other: OECD 301 D study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 301 D
- Deviations:
- no
- Principles of method if other than guideline:
- See cross-referenced study
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Details on sampling:
- Determinations of the concentration of dissolved oxygen using an oxygen electrode in duplicate vessels
were made at day 0, 7, 14, 21, 29, 35, 42, 49 and 56 for the “test suspension” and “inoculum blank with
silica gel” series, at day 0, 7, 14, 21 and 29 for the “procedure control” and “inoculum blank without silica
gel” series, and only at the start of the test and after 7 and 14 days of incubation for the “toxicity control”
series.
Temperature: Measured continuously in the growth chamber - Details on test solutions:
- See cross-referenced study
- Test organisms (species):
- aerobic microorganisms
- Details on inoculum:
- Origin: River water was sampled from “L’Adour”, situated downstream of a plant treating domestic was
tewater (Aureilhan, France).
Pre-conditioning: The river water was aerated for about 7 days before use as inoculum at the test
temperature to reduce endogenous respiration. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 28 d
- Post exposure observation period:
- None
- Hardness:
- No data
- Test temperature:
- between 20.6 and 21.3°C throughout the test
- pH:
- no data
- Salinity:
- Not applicable
- Conductivity:
- No data
- Nominal and measured concentrations:
- Nominal concentration: 2 mg/L
- Details on test conditions:
- See cross-referenced study
- Reference substance (positive control):
- no
- Key result
- Duration:
- 28 d
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: readily biodegradable at this nominal test concentration
- Details on results:
- None
- Reported statistics and error estimates:
- None
- Validity criteria fulfilled:
- yes
- Conclusions:
- The test item is considered as readily biodegradable and the tested concentration is taken as NOECmicrooorganism.
- Executive summary:
A ready biodegradability study was performed according to OECD Guideline for Testing of Chemicals No. 301 D, "Ready biodegradability – Closed Bottle Test" (1), referenced as Method C.4-E of Commission Regulation No. 440/2008 amended by Commission Regulation (EU) 2016/266 (2) and with ISO 10634 (7).
Ten BOD bottles were filled with mineral medium inoculated with river water and test item added at a nominal concentration of 2 mg/L with the help of silica gel.
Therefore, the tested concentration of 2 mg/L can be taken as conservative NOECmicrorganism.
Reference
Description of key information
The tested concentration in the ready biodegradability study (2 mg/L) is taken as conservative NOECmicrorganism.
Key value for chemical safety assessment
- EC50 for microorganisms:
- 2 mg/L
Additional information
A ready biodegradability study was performed according to OECD Guideline for Testing of Chemicals No. 301 D.
The tested concentration of 2 mg/L is taken as conservative NOECmicrorganism and is valid for key value for chemical safety assessment.
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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