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EC number: 205-746-2 | CAS number: 149-74-6
- 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:
- 2002-05-06 to 2003-02-06
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Guideline study, GLP, described in sufficient detail. The restrictions are that the analytical work done did not cover the test conditions upon which the final conclusions are based.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Nominal concentrations: 0(Control), 2.15, 4.64, 21.5, 46.4 and 100 mg/L
- Sampling method: An aliquot from the freshly prepared test media of all test concentrations was taken at the start of the test before filling the test vessels. A combined aliquot was taken from the test media of all four exposure vessels of all treatments at the end of the test.
- Sample storage conditions before analysis: Samples were stored at -20ºC before analysis. - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: The substance hydrolyses in water. An initial stock suspension was prepared at a nominal concentration of 100 mg/L by shaking for approximately 30 minutes. The suspension was then filtered through a 0.45 μm cellulose-acetate filter. The solution was diluted to prepare additional treatment levels.
- pH adjustment: A second series of treatments was prepared with adjustment of pH. The pH was adjusted to 7.9 by addition of NaOH. No precipitation was noted during or following pH adjustment.
- Controls: Dilution water - Test organisms (species):
- Daphnia magna
- Details on test organisms:
- TEST ORGANISM
- Source: IRChA, France
- Age at study initiation (mean and range, SD): 6-24 hours
- Method of breeding: Laboratory stock culture
- Feeding during test: none
ACCLIMATION
- Acclimation conditions (same as test or not): same as test
- Type and amount of food: green algae (Scenedesmus subspicatus) and a small amount of aerated sewage
- Feeding frequency: not reported - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 48 h
- Hardness:
- 250 mg/l as CaCO3
- Test temperature:
- 20+/-1ºC
- pH:
- First test (without pH adjustment): 6.95-8.12 (2.15-21.5 mg/L nominal treatments), <5.6 (46.4 mg/L nominal treatment) and <3.0 (100 mg/L nominal treatment)
Second test (with pH adjustment): 7.76-8.02 - Dissolved oxygen:
- ≥80% ASV
- Salinity:
- not applicable
- Nominal and measured concentrations:
- Nominal concentrations: 0(Control), 2.15, 4.64, 10.0, 21.5, 46.4 and 100 mg/L
In the first test (without pH adjustment), the measured concentrations of dissolved organic carbon (DOC) were close (approx 75%) to the theoretical values at the start of the test. By the end of the test the values in the 100 mg/L treatment had declined to approximately 15% of the theoretical values. The concentrations in the other treatments had remained stable. The decline in concentration in the 100 mg/L treatment was interpreted by the study report authors as being attributable to the formation of insoluble condensation products at the low pH. These products will have adsorbed to glass surfaces of the test vessels.
The results are reported with reference to nominal test concentrations.
No measured concentrations are available to support the interpretation of the second test. - Details on test conditions:
- Unless otherwise stated, these test conditions apply to both the first test and the second test.
TEST SYSTEM
- Test vessel:
- Type: open
- Material, size, fill volume: Glass, 50 ml with 50 ml of test medium
- Aeration: none
- Renewal rate of test solution (frequency/flow rate): static test
- No. of organisms per vessel: 5
- No. of vessels per concentration (replicates): 4
- No. of vessels per control (replicates): 4
- Biomass loading rate: 1 daphnid/10 ml of test medium
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Reconstituted freshwater prepared by adding salts to fully demineralised water.
- Alkalinity: 0.8 mmol/l
- Ca/mg ratio: 4:1
- Culture medium different from test medium: no
- Intervals of water quality measurement: start and end of test
OTHER TEST CONDITIONS
- Adjustment of pH: no (first test only)
- Photoperiod: 16 h light, 8 h dark
- Light intensity: 500 lux +/-20% provided by white fluorescent lights
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): immobility after 24 and 48 hours
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2.2
- Range finding study: no - Reference substance (positive control):
- no
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- 38 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- mobility
- Remarks on result:
- other: Without pH adjustment
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- < 2.15 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- mobility
- Remarks on result:
- other: Without pH adjustment
- Duration:
- 48 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- mobility
- Remarks on result:
- other: With pH adjustment
- Duration:
- 48 h
- Dose descriptor:
- NOEC
- Effect conc.:
- < 2.15 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- mobility
- Remarks on result:
- other: With pH adjustment
- Details on results:
- - Mortality of control: 5% (First test - without pH adjustment), 0% (Second test - with pH adjustment)
- Reported statistics and error estimates:
- The EC50 values were calculated by Probit Analysis using Probit Program Version 1.5, US Environmental protection Agency, 1992. The NOECs were obtained directly from the raw data.
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 48-h EC50 value of 38 mg/L and a NOEC of <2.15 mg/L have been determined for the effects of the test substance on mobility of Daphnia magna based on nominal test concentrations and under conditions with no pH adjustment. Under conditions where pH was adjusted, the corresponding values were >100 mg/L and <2.15 mg/L. Due to the very rapid hydrolysis of the registered substance, it is very likely that the test organisms were exposed to the hydrolysis products of the substance rather than the parent substance. Under the corresponding pH conditions these are expected to have been predominantly methylphenylsilanediol (CAS No. 3959-13-5) and chloride.
Reference
Table 1. Test results - first test (without pH adjustment)
Nominal concentration (mg/l) | Mean % immobile Daphnia after 24 hours | Mean % immobile Daphnia after 48 hours |
0 (Control) | 0 | 5 |
2.15 | 0 | 5 |
4.64 | 5 | 25 |
10.0 | 0 | 0 |
21.5 | 10 | 30 |
46.4 | 10 | 55 |
100 | 100 | 100 |
Table 2. Results of analysis of test media - first test (without pH adjustment)
Nominal concentration of test substance (mg/l) | Theoretical DOC concentration (mg/l) | Actual DOC concentration at start of test (mg/l) | Actual DOC concentration at end of test (mg/l) |
2.15 | 0.944 | 1.5 | 1.2 |
4.64 | 2.04 | 2.5 | 2.3 |
10.0 | 4.40 | 4.5 | 5.3 |
21.5 | 9.44 | 9.0 | 9.8 |
46.4 | 20.4 | 20.5 | 23 |
100 | 44.0 | 30.7 | 6.5 |
Note: theoretical DOC concentrations recalculated by the current reviewer.
Table 3. Test results - second test (with pH adjustment)
Nominal concentration (mg/l) | Mean % immobile Daphnia after 24 hours | Mean % immobile Daphnia after 48 hours |
0 (Control) | 0 | 0 |
2.15 | 0 | 5 |
4.64 | 0 | 10 |
10.0 | 5 | 10 |
21.5 | 5 | 15 |
46.4 | 10 | 20 |
100 | 20 | 25 |
Description of key information
Short-term toxicity to invertebrates: 48-hour EC50 >100 mg/l (nominal) (highest concentration tested) (OECD Guideline 202 (Daphnia sp. Acute Immobilisation Test)). The observations in this study are attributed to the exposure of test organisms to the hydrolysis products in the test system. The result may be expressed in terms of concentration of the hydrolysis product: 48-hour EC50 >81 mg/l as methylphenylsilanediol.
Key value for chemical safety assessment
Fresh water invertebrates
Fresh water invertebrates
- Effect concentration:
- 81 mg/L
Additional information
A 48-hour EC50 value of 38 mg/l has been determined for the effects of the test substance on mobility of Daphnia magna based on nominal test concentrations and under conditions of no pH adjustment. However, pH was reported to be <5.6 in the 46.4 mg/L nominal treatment and <3.0 in the 100 mg/L nominal treatment, therefore the result is not reliable and is disregarded. Under conditions where pH was adjusted the corresponding value was >100 mg/l. Due to the very rapid hydrolysis it is very likely that the test organisms were exposed to the hydrolysis products of the substance rather than the parent substance. The results may be expressed in terms of concentration of the hydrolysis product, methylphenylsilanediol, by applying a molecular weight correction: (MW of silanol = 154.24 / MW of parent = 191.13) * [CONCENTRATION OF PARENT = >100] = >81 mg/l.
The following data are used to support the read-across in the fish and algal trophic levels:
A 48-hour EC50 value of >100 mg/l has been determined for the effects of the supporting analogue substance, trichloro(phenyl)silane (CAS 98-13-5), on mobility of Daphnia magna. It is likely that the test organisms were predominantly exposed to the hydrolysis products of the test substance, phenylsilanetriol and hydrochloric acid.
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