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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: 242-056-0 | CAS number: 18171-19-2
- 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:
- key study
- Study period:
- 1994-05-24 to 1994-05-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- Guideline study without restrictions. The study was conducted according to the appropriate OECD test guideline, and in compliance with GLP.
- Qualifier:
- according to guideline
- Guideline:
- EU Method C.3 (Algal Inhibition test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- yes
- Details on sampling:
- - Concentrations: 34, 57, 95, 161, 284, 473 and 851 mg/L.
- Sampling method: Samples of the test media were taken for analysis at the start and end of the test.
- Sample storage conditions before analysis: not described - Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Method: Nominal test concentrations of 34, 57, 95, 161, 284, 473 and 851 mg/L were prepared by dilution of a 1000 mg/l nominal concentration stock solution. The stock solution was prepared by stirring for 18 h followed by filtration and contained 432 mg/l of dissolved organic carbon equivalent to 945 mg/L of test substance.
- Controls: Dilution water (algal growth medium) - Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Strain: CHODAT (86.81.SAG)
- Source (laboratory, culture collection): Institute for Water, Ground and Air Hygiene, Berlin (Germany)
- Age of inoculum (at test initiation): 3 days
- Method of cultivation: A pre-culture is produced from an original culture by super-inoculation three days before the test begins. From this culture the test cultures are inoculated at a density of about 20000 cells/mL. The cell concentration is determined from a calibration curve of absorbance at 685 nm versus cell density. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Hardness:
- not reported
- Test temperature:
- 24+/-2ºC
- pH:
- 8.4-8.5 at start of test
7.9-9.6 at end of test - Dissolved oxygen:
- not reported
- Salinity:
- not applicable
- Nominal and measured concentrations:
- Nominal concentrations: 0(Control), 34, 57, 95, 161, 284, 473 and 851 mg/L.
Measured concentrations were within 20% of nominal. The results are therefore reported with reference to nominal concentrations. - Details on test conditions:
- TEST SYSTEM
- Test vessel:
- Type: open Erlenmeyer flasks
- Material: glass
- Aeration: none
- Initial cells density: 20000 cells/mL
- Control end cells density: 1050000 cells/mL
- No. of vessels per concentration (replicates): 5
- No. of vessels per control (replicates): 8
GROWTH MEDIUM
- Standard medium used: yes
TEST MEDIUM / WATER PARAMETERS
- Culture medium different from test medium: no
- Intervals of water quality measurement: start and end of test
OTHER TEST CONDITIONS
- Sterile test conditions: yes
- Adjustment of pH: no
- Photoperiod: continuous
- Light intensity and quality: 8000 Lux
EFFECT PARAMETERS MEASURED:
- Determination of cell concentrations: spectrophotometer (absorption at 685 nm)
- Other:
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 1.7 - Reference substance (positive control):
- no
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 57 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- growth rate
- Remarks:
- and biomass
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 137 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 99 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 437 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 262 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- but exposure is to hydrolysis products
- Basis for effect:
- biomass
- Details on results:
- - Exponential growth in the control (for algal test): yes
- Any stimulation of growth found in any treatment: no - Reported statistics and error estimates:
- The area under the growth curve (biomass) and growth rate parameters were calculated from the cell concentration data in accordance with the description of the test method.
The EC50 values were determined by probit analysis (Cavalli-Sforza, L. (1972). Biometrie. Gustav Fischer Verlag, Stuttgart, pp. 212). The NOEC was determined by t-test. - Validity criteria fulfilled:
- yes
- Conclusions:
- A 72-hour EC50 value of 437 mg/L and NOEC of approximately 57 mg/L have been determined for the effects the test substance on growth rate of Scenedesmus subspicatus. The results are interpreted with reference to nominal concentrations of the test substance. However it is likely that the test organisms were predominantly exposed to the hydrolysis products of the substance during the study, and not the parent compound.
Reference
Table 1. Test results
Nominal test substance concentration (mg/L) | Mean cell concentration at start of test (cells/mL) | Mean cell concentration after 24 hours (cells/mL) | Mean cell concentration after 48 hours (cells/mL) | Mean cell concentration after 72 hours (cells/mL) |
0 (Control) | 20000 | 80000 | 250000 | 1050000 |
34 | 20000 | 80000 | 280000 | 1010000 |
57 | 20000 | 80000 | 270000 | 990000 |
95 | 20000 | 80000 | 250000 | 860000 |
161 | 20000 | 80000 | 230000 | 650000 |
284 | 20000 | 70000 | 160000 | 450000 |
473 | 20000 | 50000 | 100000 | 120000 |
851 | 20000 | 40000 | 40000 | 40000 |
Table 2. Results of analysis of test media
Nominal test substance concentration (mg/L) | Measured concentration at start of test (mg/L) | Measured concentration at end of test (mg/L) | Concentration used as the basis for assessing effects (mg/L) |
34 | 36 | 33 | 34 |
57 | 60 | 56 | 57 |
95 | 93 | 85 | 95 |
161 | 168 | 152 | 161 |
284 | 295 | 273 | 284 |
473 | 462 | 420 | 473 |
851 | 923 | 739 | 851 |
Description of key information
72-hour ErC50 437 mg/l, ErC10 137 mg/l and NOEC 57 mg/l (nominal concentration) (EU Method C.3 (Algal Inhibition test)), read-across from an analogous/structurally related substance, 3-chloropropyl(diethoxy)methylsilane (CAS 13501-76-3, EC 236-828-6). 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: 72-hour ErC50 321 mg/l and ErC10 101 mg/l as 3-chloropropyl(methyl)silanediol.
Key value for chemical safety assessment
- EC50 for freshwater algae:
- 321 mg/L
- EC10 or NOEC for freshwater algae:
- 101 mg/L
Additional information
No data are available for toxicity of the registration substance, 3-chloropropyl(dimethoxy)methylsilane (CAS 18171-19-2, EC 242-056-0), to algae. However, data are available from the related substance 3-chloropropyl(diethoxy)methylsilane (CAS 13501-76-3). Both substances have the same silanol hydrolysis product, 3-chloropropyl(methyl)silanediol. The other hydrolysis products are methanol and ethanol, respectively. In the test with 3-chloropropyl(diethoxy)methylsilane (CAS 13501-76-3), the observations are attributed to the exposure of test organisms to 3-chloropropyl(methyl)silanediol in the test system. There is no basis to expect that ethanol significantly influenced the results of the tests. The toxicity of ethanol is discussed further in the RAAF report for ecotoxicity attached in Annex 4 of the CSR and Section 13 of IUCLID.
A 72-hour ErC50 value of 437 mg/l, ErC10 value of 137 mg/l and NOEC value of approximately 57 mg/l have been determined for the effects of 3-chloropropyl(diethoxy)methylsilane (CAS 13501-76-3) on growth rate of Desmodesmus subspicatus. The results have been reported in terms of nominal concentrations of parent substance. Due to the hydrolysis rate of the test substance (9.5 hours at pH 7) and test media preparation methods (stirring for 18 hours prior to addition of test organisms), it is very likely that the test organisms were exposed to the hydrolysis products 3-chloropropyl(methyl)silanediol and ethanol. The results may be expressed in terms of concentration of the hydrolysis product, 3-chloropropyl(methyl)silanediol, by applying a molecular weight correction: (MW of silanol = 154.67 / MW of parent = 210.78) * [CONCENTRATION OF PARENT = EC50 437 mg/l and EC10 137 mg/l] = ErC50 321 mg/l and ErC10 101 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.