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EC number: 215-224-6 | CAS number: 1314-18-7
- 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
Toxicity to aquatic algae and cyanobacteria
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Test conducted under GLP according to standard OECD guidelines
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
Further information in a detailed justification report is included as attachment to the same record.
1. HYPOTHESIS FOR THE ANALOGUE APPROACH
For the determination of analogue in this read-across approach, the following points have been considered:
- Chemical speciation and valency (common strontium cation: Sr2+).
- The water solubility, as it provides a first indication of the availability of the metal ion in the different compartments of interest. The most simplistic approach to hazard evaluation is to assume that the specific metal-containing compound to be evaluated shows the same hazards as the most water-soluble compounds.
- In fluids of organisms and in in aqueous media, dissociation of strontium peroxide takes place immediately, resulting in formation of strontium cations (Sr2+) and oxygen. Thus, any ingestion or absorption of strontium peroxide by living organisms, in case of systemic consideration, will inevitably result of exposure to the dissociation products.
- Oxygen (formed during the dissociation of strontium peroxide) is of low (eco)toxicological relevance when ingested and taken up systemically. Thus, any possible toxicological or ecotoxicological effect triggered by strontium peroxide exposure can be attributed to strontium.
- Counter ions: the assumption that the metal ion is responsible for the common property or effect implies that the toxicity or ecotoxicity of the counter ion present in the compound will be largely irrelevant in producing the effects to be assessed.
- Likely common breakdown products via physical and/or biological processes for the targeted substance (strontium peroxide) and the analogues identified cannot present strong differences since the structures are very simple and very similar (formation of Sr2+ ion).
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES)
Source chemical information is provided in the “source” endpoint. No impurity affecting the classification is reported for the source chemical.
Information on the impurities of the target chemical are detailed in the attached report.
3. ANALOGUE APPROACH JUSTIFICATION
The main hypothesis for the analogue approach are verified. They are presented in the detailed report attached. The experimental data performed on the substance (tests performed in this REACH registration dossier on strontium peroxide) confirms the analogue approach performed (same results on analogues).
4. DATA MATRIX
A data matrix is presented in the detailed report attached. - Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Reference substance (positive control):
- yes
- Remarks:
- potassium dichromate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 43.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- element
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 104.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 43.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- element
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 104.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 43.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- element
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 104.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 43.3 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- element
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 104.7 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Details on results:
- No significant differences were recorded between the values for growth rate or yield at the limit concentration, i.e., 100 mg/L when compared to the control group. The growth and yield in lower test concentrations were stimulated rather than reduced/inhibited by the test substance. Microscopic observations at the end of the test revealed a normal and healthy appearance of the exposed cells when compared to the control.
Compliance with the Quality criteria regarding mainenance of actual concentrations was demonstrated by running a test vessel at the highest substance concentrartion 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.
Test results were in compliance with all validity criteria (minimum increase in cell density, criteria on variation (growt rates, section-by-section specific growth rates) were not exceeded. - Results with reference substance (positive control):
- The 72h-EC50 for growth reduction was 1.2 mg/L (95%CL: 0.77-2.0 mg/L).
The historical range of this value lie between 0.82 and 2.3 mg/L. - Reported statistics and error estimates:
- Recorded effects were not significant (< 10%); EC50 values could not be calculated because the test substance proved to be non-toxic within the tested concentration range.
For determination of the NOEC and the EC50 the approaches recommended in the OECD guideline 201 are used. An effect was considered to be significant if statistical analysis of the data obtained for the test concentrations compared with those obtained in the negative control revealed significant reduction of growth rate or yield inhibition (ANOVA, Tukey test, Bonferroni t-test, TOXSTAT Release 3.5, 1996, D.D. Gulley et al). - Validity criteria fulfilled:
- yes
- Conclusions:
- No statistically significant differences were found between the control and any test item concentration up to and including 100 mg test item/L. The results of the study demonstrate that the EC50 for Pseudokirchneriella subcapitata is >100 mg test item/L. The no-observed effect concentration (NOEC) is ≥104.5 mg/L strontium nitrate (based on measured concentrations). Considering the measured concentrations, the EC50 for Pseudokirchneriella subcapitata is > 43.3 mg Sr/L (measured in the highest concentration at test end). The no-observed effect concentration (NOEC) is ≥ 43.3 mg/L Sr.
Considering that these results are based on dissolved Strontium, they are considered relevant in a read-across approach. Consequently they are used for hazard and risk assessment purposes (classification; PNEC-derivation) for strontium peroxide. - Executive summary:
This study was used in a read-across approach.
The results of the study demonstrate that the EC50 for Pseudokirchneriella subcapitata is >100 mg test item/L. The no-observed effect concentration (NOEC) is ≥104.5 mg/L strontium nitrate (based on measured concentrations). Considering the measured concentrations, the EC50 for Pseudokirchneriella subcapitata is > 43.3 mg Sr/L (measured in the highest concentration at test end). The no-observed effect concentration (NOEC) is ≥ 43.3 mg/L Sr.
These data can be used for hazard and risk assessment purposes (classification; PNEC-derivation) for Strontium peroxide.
Reference
Percentage reduction of growth rate (total test period)
Nominal Concentration Strontium nitrate (mg/L | Mean growth rate - u (0 -72h) | Mean growth rate - reduction (%) |
Control | 0.05924 | |
0.10 | 0.06675 | - 12.7 |
1.0 | 0.06704 | -13.2 |
10 | 0.06628 | -11.9 |
100 | 0.05931 | -0.1 |
Description of key information
One reliable acute/chronic toxicity data point (Klimisch 1, GLP) for an algal species -the green alga Pseudokirchneriella subcapitata - has been identified.
A 72h-ErC50 and 72h-NOEC of is reported using Sr(NO3)2 as test substance.
The measured Sr-levels in solution are based on dissociate strontium. The results are thus considered relevant in a read-across approach on strontium peroxide and these data can be used for hazard and risk assessment purposes (classification; PNEC-derivation) for Strontium peroxide.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 43.3 mg/L
- EC10 or NOEC for freshwater algae:
- 43.3 mg/L
Additional information
One reliable acute/chronic toxicity data point (Klimisch 1, GLP) for an algal species - the freshwater green alga Pseudokirchneriella subcapitata - has been identified. No effect (growth rate) was noted at the highest (nominal) test concentration of 100 mg test material/L. Based on measured Sr-levels, this effects levels translates to 43.3 mg Sr/L or 104.7 mg strontium nitrate/L.
Therefore, based on measured Sr-levels in solution, the ErC50 and NOEC are >43.3 and >=43.3 mg Sr/L, respectively.
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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