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EC number: 219-842-7 | CAS number: 2550-02-9
- 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
- Justification for type of information:
- Please refer to the justification for grouping of substances provided in IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 819 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 819 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 237 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 237 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 607 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Conclusions:
- A 72-hour EC50 value of >819 mg/L and NOEC of 237 mg/L have been determined for the effects of the test substance on growth rate and biomass of Scenedesmus subspicatus. The study is considered reliable.
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1993-07-06 to 1993-07-09
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- 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:
- The Dissolved Organic Carbon (DOC) concentration of the stock solution that was used to prepare the test media was determined and used as the basis for calculating the nominal treatment concentrations.
- Vehicle:
- no
- Details on test solutions:
- Six nominal test concentrations of 55, 91, 155, 273, 455 and 819 mg/L. 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 to be 408 mg/L, equivalent to a test substance concentration of 910 mg/L..
- Test organisms (species):
- Desmodesmus subspicatus (previous name: Scenedesmus subspicatus)
- Details on test organisms:
- TEST ORGANISM
- Strain: 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. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Hardness:
- Not reported
- Test temperature:
- 24 +/-2ºC
- pH:
- Start of test: 6.9 - 7.4
End of test: 4.5 - 8.6 - Dissolved oxygen:
- Not applicable
- Salinity:
- Not applicable
- Nominal and measured concentrations:
- Nominal concentrations: 0 (Control), 55, 91, 155, 273, 455 and 819 mg/L
- 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: 900000 cells/ml
- No. of vessels per concentration (replicates): 4 or 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 (with observation intervals if applicable): Growth rate and biomass
- 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:
- EC50
- Effect conc.:
- > 819 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 819 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 237 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 237 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- biomass
- Duration:
- 72 h
- Dose descriptor:
- EC10
- Effect conc.:
- 607 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- growth rate
- Reported statistics and error estimates:
- The effects on growth were insufficient to determine an EC50 value. The EC10 value was determined by Probit analysis. The NOEC was determined by visual examination of the raw data.
- Validity criteria fulfilled:
- yes
- Conclusions:
- A 72-hour EC50 value of >819 mg/L and NOEC of 237 mg/L have been determined for the effects of the test substance on growth rate and biomass of Scenedesmus subspicatus. The study is considered reliable.
Referenceopen allclose all
Table 1. Test results
Nominal test concentration (mg/L) | Mean cell density at start of test (cells/mL) | Mean cell density after 24 hours (cells/mL) | Mean cell density after 48 hours (cells/mL) | Mean cell density after 72 hours (cells/mL) |
0 (Control) | 20000 | 80000 | 250000 | 900000 |
55 | 20000 | 80000 | 280000 | 990000 |
91 | 20000 | 80000 | 280000 | 940000 |
155 | 20000 | 80000 | 310000 | 1010000 |
273 | 20000 | 80000 | 290000 | 880000 |
455 | 20000 | 70000 | 250000 | 990000 |
819 | 20000 | 70000 | 230000 | 500000 |
Description of key information
A 72-hour EC50 value of >819 mg/L (EU Method C.3, read across from CAS 5089-70-3).
Key value for chemical safety assessment
Additional information
Note: An acute fish study, a daphnia test and a biodegradation screening study are currently ongoing for the registered substance (i.e. triethoxy(propyl)silane (CAS 2550-02-9)) in order to support the read across from (3-chloropropyl) triethoxysilane (CAS 5089-70-3) . This dossier will be updated once the final study reports are available.
Measured data were not available for triethoxy(propyl)silane. It was considered appropriate to read across from the structurally analogous substance, (3-chloropropyl)triethoxysilane (5089-70-3). A 72-hour EC50value of >819 mg/l and NOEC of 237 mg/l have been determined for the effects of the test substance on the growth rate and biomass of Scenedesmus subspicatus. The study was conducted according to EU Method C.3 (Algal Inhibition test) and is considered reliable for assessment.
Additional good quality data for the analogue substance,trimethoxypropylsilane, have been read across for triethoxypropylsilane. Both substances share the same silanol hydrolysis product, propylsilanetriol; the other hydrolysis products being ethanol and methanol.A 72 hr EC50of 913 mg/l and NOEC of ≥913 mg/l have been deteremined for the effect on growth rate on the algae Scenedesmus subspicatus (new name: Desmodesmus subspicatus) (EU Method C.3 (Algal Inhibition test) based on nominal concentrations of the substance.
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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