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EC number: 220-449-8 | CAS number: 2768-02-7
- 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
Short-term toxicity to aquatic invertebrates
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to aquatic invertebrates
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1993-06-01 to 1993-06-03
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.2 (Acute Toxicity for Daphnia)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- The concentration of hydrolysis products in stock solution determined by Total Organic Carbon analysis. The stock solution concentration (464 mg/l equivalent to a test substance concentration of 1145 mg/L) was used as the basis for determining the concentrations in the test media.
- Vehicle:
- no
- Details on test solutions:
- - Method: Test media prepared by dilution of a 1000 mg/L stock solution prepared by mixing for 18 h followed by filtration. TOC concentration of stock solution determined.
- Treatments: Control and nominal test concentrations of 57, 80, 115, 160, 229, 321 and 458 mg/L. - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Common name: Daphnia magna
- Strain: Clone 5
- Source: Stock culture
- Age at study initiation (mean and range, SD): <24 h
- Method of breeding: Parthenogenetic reproduction
- Feeding during test: None
ACCLIMATION
- Acclimation conditions (same as test or not): yes
- Type and amount of food: sufficient to be consumed each day leaving no residue
- Feeding frequency: daily - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Post exposure observation period:
- none
- Hardness:
- The sum of the Ca2+ and Mg2+ ions was 2.5 mmol
- Test temperature:
- 20 ±1ºC
- pH:
- 7.0 - 7.2
- Dissolved oxygen:
- 6.5 - 8.1 mg/L
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Control and nominal test concentrations of 57, 80, 115, 160, 229, 321 and 458 mg/L.
- Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type: open
- Material, size, headspace, fill volume: glass cylinder containing 10 ml of test medium
- Aeration: none
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Elendt M4 medium
- Intervals of water quality measurement: end of test
OTHER TEST CONDITIONS
- Photoperiod: Dark
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : Immobilization after 24 and 48 h exposure
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.4
STATISTICS
EC50 and confidence interval determined by Probit analysis - Reference substance (positive control):
- yes
- Remarks:
- Potassium dichromate
- Duration:
- 24 h
- Dose descriptor:
- EC50
- Effect conc.:
- 297.2 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 223.9 - 224.2
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 168.7 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mobility
- Remarks on result:
- other: 126.9 - 224.2
- Details on results:
- - Mortality of control: 0
- Results with reference substance (positive control):
- - EC50: >0.9, <1.9 mg/L
- Reported statistics and error estimates:
- The EC50 value and its 95% confidence interval was calculated by Probit analysis.
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 48-h EC50 value of 168.7 mg/L has been determined for the effects of the test substance on mobility of Daphnia magna. A NOEC was not determined in the test. It is likely that the test organisms were primarily exposed to the hydrolysis products of the substance.
Reference
Table 1. Test results
Nominal test substance concentration (mg/L) | Percentage immobile Daphnia after 24 hours | Percentage immobile Daphnia after 48 hours |
0 (Control) | 0 | 0 |
57 | 5 | 25 |
80 | 5 | 25 |
115 | 5 | 35 |
160 | 0 | 35 |
229 | 25 | 45 |
321 | 55 | 75 |
458 | 90 | 100 |
Description of key information
48-hour EC50: 168.7 mg/L for effects of the test substance on mobility of Daphnia magna. It is likely that the test organisms were primarily exposed to the hydrolysis products of the substance. The EC50 is equivalent to 121 mg/L when expressed in terms of the silanol hydrolysis product, vinylsilanetriol (CAS 143-48-6).
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 121 mg/L
Additional information
A 48-hour EC50 value of 168.7 mg/L (nominal concentration) has been determined for the effects of the test substance on mobility of Daphnia magna. It is likely that the test organisms were primarily exposed to the hydrolysis products of the substance. The results may be expressed in terms of the silanol hydrolysis product by adjusting for the respective molecular weights: MW hydrolysis product/MW parent * E(L)C50 or NOEC value, thus 106.15/148.24 * EC50 of 168.7 mg/L = 121 mg/L as vinylsilanetriol (CAS 143-48-6).
The results of this test were selected in preference to those of four other tests because a definitive EC50 value was determined and it was judged to be more reliable.
The following result is from a reliable study included as supporting data:
48-hour EC50 >100 mg/L for effects of the test substance on mobility of Daphnia magna (Dow Corning Corporation, 1979).
Three further studies, for which reliability could not be ascertained, are also included in the dataset:
48-hour EC50 >100 mg/L for effects of the test substance on mobility of Daphnia magna (Bement, 2001).
EC50 360 mg/L for effects of the test substance on mobility of Daphnia magna (Chandra, 1997).
48-hour EC50 >100 mg/L for effects of the test substance on mobility of Daphnia magna (MOE Japan, 2005).
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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