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EC number: 201-083-8 | CAS number: 78-10-4
- 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 fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1993-10-11 to 1993-10-15
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.1 (Acute Toxicity for Fish)
- Version / remarks:
- Cited as Directive 92/69/EEC, C.1
- GLP compliance:
- yes
- Analytical monitoring:
- yes
- Details on sampling:
- Samples of freshly prepared test media were taken at the start of each successive 24 hour exposure period (0, 24, 48 and 72 hours). Samples of old test medium were taken at the end of the first 24-hour exposure period in order to assess the stability of the exposure concentrations.
- Vehicle:
- no
- Details on test solutions:
- A stock solution was prepared by adding the test substance to potable water at the rate of 1 g/L. After mixing the medium was filtered and the aqueous phase used as the test medium. The average measured Dissolved Organic Carbon Concentration determined in the fresh test medium over the course of the test (245 mg/L) was used as the basis for expressing the test results.
- Test organisms (species):
- Danio rerio (previous name: Brachydanio rerio)
- Details on test organisms:
- TEST ORGANISM
- Common name: Zebrafish
- Source: West Aquarium, Bad Lauterburg, Germany
- Length at study initiation: 3.0+/-0.5 cm
- Feeding during test: none
ACCLIMATION
- Acclimation period: 14-days
- Acclimation conditions: same as test
- Type and amount of food: Tetramin® at 1% of body weight
- Feeding frequency: Daily
- Health and pre-treatment: The specimens were pre-conditioned (treatment: 3x per week with malachite green) and subjected to a 14-day quarantine. They were used in testing only after this treatment. Only specimens displaying normal behaviour at the beginning of the test and free of obvious disease were used in the study. Fish were not fed during the test. - Test type:
- semi-static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 96 h
- Hardness:
- 10.7 ºdH
- Test temperature:
- 20+/-1ºC
- pH:
- 7.5-8.4
- Dissolved oxygen:
- 4.3-8.9 mg/L (the low value of 4.3 mg/L did not affect the outcome of the test)
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal loading used to prepare test medium: 1000 mg/L
Mean measured DOC concentration in the test medium: 245 mg/L
The mean measured DOC concentration has been used as the basis for expressing the test results. - Details on test conditions:
- TEST SYSTEM
- Test vessel: 20 litre aquarium
- Type (delete if not applicable): open
- Aeration: Yes, continuous
- Renewal rate of test solution: daily
- No. of organisms per vessel: 10
- No. of vessels per concentration (replicates): 1
- No. of vessels per control (replicates): 1
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Potable water from Gelsenwasser AG
OTHER TEST CONDITIONS
- Adjustment of pH: No
- Photoperiod: 16 hours light, 8 hours dark
EFFECT PARAMETERS MEASURED: Daily mortalities
TEST CONCENTRATIONS
- Spacing factor for test concentrations: Limit test - Reference substance (positive control):
- no
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- >= 245 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- > 245 mg/L
- Nominal / measured:
- meas. (arithm. mean)
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Details on results:
- - Mortality of control: 0
- Reported statistics and error estimates:
- There were no mortalities observed in the test and therefore statistical analysis of the results was not required.
- Sublethal observations / clinical signs:
Table 1. Results of analysis of test media
Nominal loading of test substance (mg/L) Measured DOC concentration in fresh medium at start of test (mg/L) Measured DOC concentration in old medium after 24 hours (mg/L) Measured DOC concentration in fresh medium after 24 hours (mg/L) Measured DOC concentration in fresh medium after 48 hours (mg/L) Measured DOC concentration in fresh medium after 72 hours (mg/L) Mean measured DOC concentration (mg/L) 1000 316 247 227 281 156 245 Table 2. Test results
Mean measured DOC concentration (mg/L) Percentage mortality after 24 hours Percentage mortality after 48 hours Percentage mortality after 72 hours Percentage mortality after 96 hours 0 (Control) 0 0 0 0 245 0 0 0 0
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 96-hour LC50 of >245mg/L and a NOEC of ≥245 mg/L have been determined for the effects of the test substance on mortality of Brachydanio rerio. It is likely that the test organisms were exposed to the hydrolysis products of the substance.
Reference
Description of key information
Short-term toxicity to fish: 96-hour LC50 >245 mg/l (mean measured): (highest concentration tested) (test guideline EU method C.1 (Acute Toxicity for Fish)). The LC50 is equivalent to >113 mg/l when expressed in terms of the silanol hydrolysis product, monosilicic acid.
Key value for chemical safety assessment
Additional information
A 96-hour LC50 value of >245 mg/l (mean measured DOC) (highest concentration tested) has been determined for the effects of tetraethyl orthosilicate (CAS 78-10-4) on mortality of Danio rerio (Hüls, 1993) in accordance with test guideline EU method C.1 (Acute Toxicity for Fish) and in compliance with GLP. In view of the test media preparation method/exposure regime it is likely that the test organisms were exposed predominantly to the hydrolysis products of the tested substance. The results may be expressed in terms of concentration of the hydrolysis product, monosilicic acid, by applying a molecular weight correction: (MW of silanol = 96.1 / MW of parent = 208.33) * >245 = >113 mg/l.
Refer to IUCLID Section 6, CSR Section 7.0, for further discussion of the approach to chemical safety assessment.
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