Registration Dossier
Registration Dossier
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: 221-435-4 | CAS number: 3091-25-6
- 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

Toxicity to aquatic algae and cyanobacteria
Administrative data
- Endpoint:
- toxicity to aquatic algae and cyanobacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 12-15 Novemer 2002
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Study conducted in compliance with agreed protocols, with no or minor deviations from standard test guidelines and/or minor methodological deficiencies, which do not affect the quality of the relevant results. Study was in compliance with OECD Good Laboratory Practice (GLP). Derivations were involved in obtaining the toxicity values using statistical model.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 003
- Report date:
- 2003
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 201 (Alga, Growth Inhibition Test)
- Deviations:
- not specified
- GLP compliance:
- yes
Test material
- Reference substance name:
- Trichlorooctylstannane
- EC Number:
- 221-435-4
- EC Name:
- Trichlorooctylstannane
- Cas Number:
- 3091-25-6
- Molecular formula:
- C8H17Cl3Sn
- IUPAC Name:
- trichlorooctylstannane
- Details on test material:
- - Name of test material (as cited in study report): Trichlorooctylstannane
- Molecular formula (if other than submission substance): C8Hl7CI3Sn
- Molecular weight (if other than submission substance): 338.3 g/mol
- Physical state: colourless liquid
- Analytical purity: 100.0% n-octyltin trichloride
Constituent 1
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
No information
Sampling and analysis
- Analytical monitoring:
- yes
- Details on sampling:
- At the start of the growh inhibition test, duplicate 100 mL samples were taken from all media (without algae) containing all nominal test substance concentrations tested, together with a control. At the end of the test, duplicate 100 mL samples were taken from the media containing the same test substance concentrations with algae. One of the duplicate sample series at the start and at the end of the test was analysed. The remaining samples were stored in a freezer to allow later analysis.
Test solutions
- Vehicle:
- not specified
- Details on test solutions:
- The test substance was added directly to an appropriate quantity of algal medium in an Erlenmeyer flask, followed by stirring for 16-20 hours using a magnetic stirrer. The stirring was such that the vortex created extended to ca. 1/3 of the dept of the fluid column. Following stirring, the medium was allowed to stand for ca. 4 hours to enable phase separation. The clear aqueous phase was tapped and diluted to achieve a concentration series. The first 100 mL was discarded. The saturated solutions were diluted with algal medium to prepare the test dilutions.
Test organisms
- Test organisms (species):
- other: green alga (Scenedesmus subspicatus (SAG 86.81)
- Details on test organisms:
- The freshwater green alga Scenedesmus subspicatus (SAG 86.81), which belongs to the order of Chlorococcales (class Chlorophyceae), was used as the test organism. The culture was supplied by the Collection of Algal Cultures, Institue for Plant Phsiology, University of Gottingen, Nikolausberger Weg 18, D-37073 Gottingen, Germany. A pre-culture of algae in the exponential growth phase was prepared as detailed in OECD Guideline no. 201, using hte medium described in 2.4. The initial inoculum cell density was 0.3 x 10^4 cells/mL to obtain the appropriate biomass level in the test medium.
Study design
- Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 72 h
- Post exposure observation period:
- No information.
Test conditions
- Hardness:
- No information.
- Test temperature:
- 21.7 - 23.6 ºC.
- pH:
- Ranged from 7.5 to 8.0.
- Dissolved oxygen:
- No information.
- Salinity:
- No information.
- Nominal and measured concentrations:
- No information.
- Details on test conditions:
- Light intensity 81 - 100 µmols/s/m^2.
- Reference substance (positive control):
- not specified
Results and discussion
Effect concentrationsopen allclose all
- Duration:
- 72 h
- Dose descriptor:
- NOEC
- Effect conc.:
- 0.045 mg/L
- Basis for effect:
- growth rate
- Duration:
- 72 h
- Dose descriptor:
- EC50
- Effect conc.:
- 0.215 mg/L
- Basis for effect:
- growth rate
- Details on results:
- The study meet validty criteria in OECD test guideline 201.
- Results with reference substance (positive control):
- No information.
- Reported statistics and error estimates:
- The toxicity estimates derived from the statistical model demonstrated that MOTC had a significant adverse effect on the growth rate. The lower EbC50 value is therefore considered to have no toxicological relevance.
Any other information on results incl. tables
No other information.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- yes
- Conclusions:
- The 72-h toxicity of trichlorooctylstannane to fresh water green alga (Scenedesmus subspicatus) (ErC50) was 0.215 mg/L. The NOEC was 0.045 mg/L.
- Executive summary:
The toxicity of trichlorooctylstannane to fresh water green alga (Scenedesmus subspicatus) was determined in a 72 -h growth inhibition test according to OECD Guideline 201 (Alga, Growth Inhibition Test) and in compliance with the OECD principles of Good Laboratory Practices (GLP). The ErC50 was determined to be 0.215 mg/L based on the average measured concentrations of the test substance. The NOEC was 0.045 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.
