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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 254-996-9 | CAS number: 40601-76-1
- 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:
- supporting study
- Study period:
- 2012-05-21 - 2012-05-24
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Version / remarks:
- 2006
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- ISO 8692 (Water Quality - Fresh Water Algal Growth Inhibition Test with Scenedesmus subspicatus and Selenastrum capricornutum)
- Version / remarks:
- 2004
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Version / remarks:
- 2009
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: Guidance document on aquatic toxicity testing of difficult substances and mixtures, OECD series on testing and assessment number 23, December 14, 2000.
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Remarks:
- Further discussion is provided in the attached background document.
- Details on sampling:
- Samples for possible analysis were taken from all test concentrations and the control according to the schedule below.
Frequency: at t=0 h, t=24 h and t=72 h
Volume: 2 ml
Storage: Samples were stored in a freezer until analysis.
At the end of the exposure period, the replicates with algae were pooled at each concentration before sampling.
Compliance with the Quality criteria regarding maintenance of actual concentrations was demonstrated by running a test vessel at the highest substance concentration but without algae and samples for analysis were taken at the start, after 24 hours of exposure and at the end of the test period.
Additionally, singular reserve samples of 2 ml were taken from all test solutions for possible analysis. If not already used, these samples were stored in a freezer for a maximum of three months after delivery of the draft report, pending on the decision of the sponsor for additional analysis. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
The batch of CYANOX® 1790 Antioxidant tested was an off white powder with a purity >96% and the substance was not completely soluble in test medium at the loading rate initially prepared.
Preparation of test solutions started with a loading rate of 100 mg/l a 2-day period of magnetic stirring. The obtained mixture was filtered through a 0.45 µm membrane filter (RC55, Whatman) and used as the highest concentration. The lower test concentrations were prepared by subsequent dilutions of the highest concentration in test medium. The final test solutions were all clear and colourless.
After preparation, volumes of 50 ml were added to each replicate of the respective test concentration. Subsequently, 1 ml of an algal suspension was added to each replicate providing a cell density of
10E4 cells/ml. - Test organisms (species):
- Raphidocelis subcapitata (previous names: Pseudokirchneriella subcapitata, Selenastrum capricornutum)
- Details on test organisms:
- TEST ORGANISM
- Common name: Pseudokirchneriella subcapitata
- Strain: NIVA CHL 1
- Source (laboratory, culture collection): in-house culture
- Age of inoculum (at test initiation): 3 days before the start of the test, cells from the algal stock culture were inoculated in culture medium at a cell density of 1 x 10E4 cells/ml.
- Method of cultivation: Algae stock cultures were started by inoculating growth medium with algal cells from a pure culture on agar. The suspensions were continuously aerated and exposed to light (60 to 120 µE/m2/s when measured in the photosynthetically effective wavelength range of 400 to 700 nm) in a climate room at a temperature of 21-24°C. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 72 h
- Post exposure observation period:
- no
- Hardness:
- 0.24 mmol(24 mg CaCO3/L)
- Test temperature:
- 21.9 and 24.5°C
- pH:
- 8.0-8.2
- Dissolved oxygen:
- not measured
- Salinity:
- not measured
- Nominal and measured concentrations:
- Solutions containing 0.1, 1.0, 10 and 100% of a 0.45 µm filterate prepared at a loading rate of 100 mg/l.
Samples taken from all groups were analysed. The actual concentration in the undiluted filtrate was 0.012 mg/l at the start of the test. Note that this concentration is below the limit of quantification of the analytical method, i.e. 0.1 mg/l, and therefore, is only indicative. However, it was close to the provided solubility of the test substance in water, i.e. <0.02 mg/l. The measured concentration in this group dropped below the limit of detection of the analytical method, i.e. below 0.005 mg/l, after 24 hours of exposure. In the lower groups the actual concentrations were below the limit of detection from the start of the test. - Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 ml, all-glass, containing 50 ml of test solution
- Type (delete if not applicable): open
- Initial cells density: 10e4 cell/ml
- Control end cells density: 3015000 cells/ml
- No. of vessels per concentration (replicates): 6 for limit concentration, 3 for lower concentrations
- No. of vessels per control (replicates): 6
- No. of vessels per vehicle control (replicates): not applicable
- Incubation: Capped vessels were distributed at random in the incubator and as such were daily repositioned. During incubation the algal cells were kept in suspension by continuous shaking.
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- M2; according to the OECD 201 Guideline, formulated using Milli-RO water (tap-water purified by reverse osmosis; Millipore Corp., Bedford, Mass., USA)
OTHER TEST CONDITIONS
- Sterile test conditions: no
- Adjustment of pH: no
- Photoperiod: continous
- Light intensity and quality: 72 to 83 uE.m-2.s-1.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
- Determination of cell concentrations: [ spectrophotometer], t=0, 24, 48 and 72 h
- 72 h NOErC, 72 h NOEyC, 72 h ErC50, 72 h EyC50
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 10
- Range finding study: the study was performed as a combined limit/range-finding test - Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.012 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 0.012 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- other: yield
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.012 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.012 mg/L
- Nominal / measured:
- meas. (initial)
- Conc. based on:
- test mat.
- Basis for effect:
- other: yield
- Details on results:
- - Exponential growth in the control (for algal test): yes
- Microscopic observations at the end of the test revealed a normal and healthy appearance of the exposed cells when compared to the control.
Further discussion on the approach used to report the results (measured vs. nominal concentrations) can be found in the attached background document. - Results with reference substance (positive control):
- - Results with reference substance valid? yes
- EC50: 0.98 mg/l with a 95% confidence interval ranging from 0.74 to 1.3 mg/l (growth rate reduction) - Reported statistics and error estimates:
- - For determination of the NOEC and the EC50 the approaches recommended in the OECD guideline 201 were used.
- Statistical analysis of the data was not needed as the effects recorded were not significant (<10%).
- No EC50 and EC10-values could be calculated because the test substance proved to be non-toxic (EC10 > maximum soluble concentration). - Validity criteria fulfilled:
- yes
- Conclusions:
- Under the conditions of the present study, no reduction of growth rate or inhibition of yield was recorded at any of the concentrations.
- Executive summary:
Following OECD TG 201 and under GLP conditions, no reduction of growth rate or inhibition of yied was recorded with Pseudokirchneriella subcapitatata at any of the concentrations of Cyanox 1790 Antioxidant tested.
The EC50 for growth rate reduction (ERC50: 0-72h) and the EC50 for yield inhibition (EYC50: 0-72h) were beyond the range tested, i.e. exceeded the initially measured concentration of 0.012 mg/l.
The NOEC for both growth rate reduction and yield inhibition was 0.012 mg/l, i.e. solubility limit in medium.
Due to the very low solubility of the test item in water, concentration levels that might be toxic for algae could not be reached.
Reference
Table: Calculation of growth rate (section-by-section)
%filtrate prep. At 100 mg/l | Vessel number | Growth rate (µ) | Growth rate reduction (%) | ||||
0-24h | 24-48h | 48-72h | 0-24h | 24-48h | 48-72h | ||
control | 1 2 3 4 5 6 | 0.10694 0.10629 0.09974 0.09937 0.11021 0.10878 | 0.07538 0.06757 0.07585 0.07106 0.07902 0.07357 | 0.05774 0.06093 0.06149 0.06195 0.05255 0.05797 | |||
Mean CV | 0.10522 4% | 0.07374 5% | 0.05877 6% | ||||
The mean CV for section-by-section specific growth rate was 26% | |||||||
0.10 | 1 2 3 | 0.10006 0.10028 0.10375 | 0.06952 0.07718 0.06672 | 0.06161 0.06136 0.06377 | 5 5 1 | 6 -5 10 | -5 -4 -9 |
1.0 | 1 2 3 | 0.10478 0.10083 0.10134 | 0.07186 0.07054 0.07099 | 0.06082 0.06289 0.06135 | 0 4 4 | 3 4 4 | -3 -7 -4 |
10 | 1 2 3 | 0.10050 0.10354 0.10575 | 0.07487 0.07007 0.06863 | 0.06002 0.06433 0.06003 | 4 2 -1 | -1 5 7 | -2 -9 -2 |
100 (0.012) | 1 2 3 4 5 6 | 0.10437 0.10521 0.10434 0.10019 0.10327 0.10194 | 0.07273 0.07339 0.07397 0.07849 0.06968 0.07107 | 0.05809 0.06101 0.05998 0.06192 0.06092 0.06258 | 1 0 1 5 2 3 | 1 0 0 -6 6 4 | 1 -4 -2 -5 -4 -6 |
( ) - initially measured concentration (mg/l)
Description of key information
In a 72-h aquatic toxicity study in algae, the test material produced no significant reduction in the growth rate up to the highest concentration tested.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 100 mg/L
- EC10 or NOEC for freshwater algae:
- 100 mg/L
Additional information
In a 72 -h study conducted according to OECD Guideline 201, the test material did not produce significant toxicity in the freshwater algae species, Pseudkirchnerella subcapitata, up to a highest nominal concentration of 100 mg/L. The measured actual concentration of the test material at the start of testing was 0.012 mg/L. The EC50 was reported as > 0.012 mg/L. The NOEC was reported as 0.012 mg/L. Key values for purposes of the chemical safety assessment will be reported as the nominal concentration (100 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.