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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 220-668-9 | CAS number: 2855-27-8
- 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 aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1993
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Guideline 92/69/EEC
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: A saturated stock solution of 1g/L (nominal) has been tested by DOC analysis. The DOC was 1.98 mg/L and the stock soultion was diluted to the test concentratios 0.13 mg/L; 0.22 mg/L; 0.37 mg/L; 0.66 mg/L; 1.10 mg/L; and 1.98 mg/L.
- Sampling method: The DOC content of the stock solution has been meausured. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: A suspension of 1 g/L of the test substance in purified water has been stirred for 18 hours. Then the solution was filtered and the carbon content was determined. The DOC content of the solution is 1.98 mg/L corresponding to 2.2 mg/L product. This solution was used as stock solution. The test concentrations were based on the product and calculated from the DOC of the stock solution. The test concentrations of 0.13 mg/L, 0.22 mg/L, 0.37 mg/L, 0.66 mg/L, 1.10 mg/L, and 1.98 mg/L were tested.
- Controls: test water without test substance
- Evidence of undissolved material (e.g. precipitate, surface film, etc.): not specified - Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Common name: green algae
- Strain: Scenedesmus subspicatus (CHODAT 86.81 SAG)
- Source (laboratory, culture collection): Institute for water, soil, and air hygiene, Berlin, and breeding in the laboratory
- Age of inoculum (at test initiation): 3 days before test start a preculture was inoculated from a stock culture.
ACCLIMATION
- Acclimation period: 3 days before test start a preculture was inoculated from a stock culture.
- Culturing media and conditions (same as test or not): not specified - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Test temperature:
- 24 +/- 2 °C
- pH:
- at test start: 7.4 - 7.6
at test end: 8.5 - 8.6 - Nominal and measured concentrations:
- DOC of the stock solution 1.98 mg/L corresponding to 2.2 mg/L product concentration . Test concentration (calculated from stock solution) 0.13 mg/L; 0.22 mg/L; 0.37 mg/L; 0.66 mg/L; 1.10 mg/L; and 1.98 mg/L.
- Details on test conditions:
- TEST SYSTEM
- Test vessel: Erlenmeyer flask
- Type (delete if not applicable): open / closed
- Material, size, headspace, fill volume: glass, steril
- Aeration: yes
- Initial cells density: 20000 cells/mL
- Control end cells density: 81* 10^4 cells/mL
- No. of vessels per concentration (replicates): 5
- No. of vessels per control (replicates): 8
GROWTH MEDIUM
- Standard medium used: not specified, according to guideline
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Light intensity and quality: approx. 8000 Lux, white light
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : number of cell
- Determination of cell concentrations: photometric measurement. Absorption at 685 nmm, calculation of cells/mL by calibration curve - Reference substance (positive control):
- no
- Key result
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1.98 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: highest solubility under test conditions
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- > 1.98 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: highest solubility under test conditions
- Duration:
- 72 h
- Dose descriptor:
- EC90
- Effect conc.:
- > 1.98 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Remarks on result:
- other: highest solubility under test conditions
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1.98 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 1.7 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 1.1 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Details on results:
- Based on the growth rate, an EC50 (0-72h) of >1.98 mg/L and an EC10 (0-72 h) of >1.98 mg/L were found. All concentration are based on the concentration of the test substance. Based on the biomass, an EbC50 of >1.98 mg/L and an EbC10 of 1.7 mg/L were determined. The NOEC based on biomass is 1.1 mg/L. The concentration of 1.98 mg/L is the highest solubilty under test conditions.
- Reported statistics and error estimates:
- It was not possible to calculate EC values according to probit transformation of the percental inhibition values with an regression analysis. The EC10 value has been determined graphically.
- Validity criteria fulfilled:
- yes
- Remarks:
- Valdity criteria are not specified in the report, but the criteria according to the guideline OECD202 (before 2006) are fulfilled. Also the validity criteria of the newer guideline (OECD 202, 2006/2011) would be met.
- Conclusions:
- Based on the growth rate, an EC50 (0-72h) of >1.98 mg/L and an EC10 (0-72 h) of >1.98 mg/L were found. The concentration of 1.98 mg/L corresponds to the highest solubilty under test conditions.
Reference
Description of key information
A toxicity test on Desmodesmus subspicatus with 1,2,4 -Trivinylcyclohexane revealed an ErC50 >1.98 mg/L and an ErC10 (0-72 h) of >1.98 mg/L based on the growth rate.
Key value for chemical safety assessment
Additional information
A toxicity test on Desmodesmus subspicatus (previously Scenedesmus subspicatus) with 1,2,4 -Trivinylcyclyhexane is available and has been performed according to guideline 92/69/EEC and OECD201 (before 2006). The study has been conducted in accordance to GLP requirements and has acceptable restrictions (analytical method for measurement of the test substance concentration is not substance-specific), but is well documented.
Based on the growth rate, an ErC50 (0-72h) of >1.98 mg/L and an ErC10 (0-72 h) of >1.98 mg/L were found. The concentration of 1.98 mg/L corresponds to the highest solubilty under test conditions.
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.